### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = CYP2A6) # charset = UTF-8 ## Genes ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{name}}" "{{chromosome}}" "{{chrom_band}}" "{{imprinting}}" "{{refseq_genomic}}" "{{refseq_UD}}" "{{reference}}" "{{url_homepage}}" "{{url_external}}" "{{allow_download}}" "{{id_hgnc}}" "{{id_entrez}}" "{{id_omim}}" "{{show_hgmd}}" "{{show_genecards}}" "{{show_genetests}}" "{{show_orphanet}}" "{{note_index}}" "{{note_listing}}" "{{refseq}}" "{{refseq_url}}" "{{disclaimer}}" "{{disclaimer_text}}" "{{header}}" "{{header_align}}" "{{footer}}" "{{footer_align}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{updated_by}}" "{{updated_date}}" "CYP2A6" "cytochrome P450, family 2, subfamily A, polypeptide 6" "19" "q13.2" "no" "NG_008377.1" "UD_132118378151" "" "https://www.LOVD.nl/CYP2A6" "" "1" "2610" "1548" "122720" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "https://databases.lovd.nl/shared/refseq/CYP2A6_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2018-10-27 11:33:59" "00000" "2025-05-05 21:14:00" ## Transcripts ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{geneid}}" "{{name}}" "{{id_mutalyzer}}" "{{id_ncbi}}" "{{id_ensembl}}" "{{id_protein_ncbi}}" "{{id_protein_ensembl}}" "{{id_protein_uniprot}}" "{{remarks}}" "{{position_c_mrna_start}}" "{{position_c_mrna_end}}" "{{position_c_cds_end}}" "{{position_g_mrna_start}}" "{{position_g_mrna_end}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00005994" "CYP2A6" "cytochrome P450, family 2, subfamily A, polypeptide 6" "001" "NM_000762.5" "" "NP_000753.3" "" "" "" "-21" "1743" "1485" "41356352" "41349443" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 7 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00000" "Healthy/Control" "Healthy individual / control" "" "" "" "" "" "00000" "2012-07-26 17:29:43" "" "" "00198" "?" "unclassified / mixed" "" "" "" "" "" "00006" "2013-09-13 14:21:47" "00006" "2024-11-23 09:38:12" "00639" "cancer, lung" "cancer, lung (adenocarcinoma)" "" "211980" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "01269" "DMBCYP2A6" "metabolism, drug, resistance, coumarin" "AD" "122700" "" "autosomal dominant" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "01586" "nicotine" "addiction, nicotine, susceptibility to" "" "188890" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2023-10-23 16:02:32" "04264" "DMBp" "metabolism, drug, poor" "" "" "" "" "" "00006" "2015-05-14 15:38:48" "00006" "2021-12-11 13:56:28" "04272" "DMBr" "metabolism, drug, rapid" "" "" "" "" "" "00006" "2015-05-14 16:05:54" "00006" "2021-12-11 13:56:28" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 3 "{{geneid}}" "{{diseaseid}}" "CYP2A6" "00639" "CYP2A6" "01269" "CYP2A6" "01586" ## Individuals ## Do not remove or alter this header ## ## Count = 136 "{{id}}" "{{fatherid}}" "{{motherid}}" "{{panelid}}" "{{panel_size}}" "{{license}}" "{{owned_by}}" "{{Individual/Reference}}" "{{Individual/Remarks}}" "{{Individual/Gender}}" "{{Individual/Consanguinity}}" "{{Individual/Origin/Geographic}}" "{{Individual/Age_of_death}}" "{{Individual/VIP}}" "{{Individual/Data_av}}" "{{Individual/Treatment}}" "{{Individual/Origin/Population}}" "{{Individual/Individual_ID}}" "00183692" "" "" "" "1" "" "00008" "" "reference haplotype/ Incr.?/ has also been called CYP2A6*1E / previously CYP2A6*1B1" "" "" "" "" "0" "" "" "" "" "00183693" "" "" "" "1" "" "00008" "" "reference haplotype/ has also been called CYP2A6*1B" "" "" "" "" "0" "" "" "" "" "00183694" "" "" "" "1" "" "00008" "" "reference haplotype/ has also been called CYP2A6*1B3" "" "" "" "" "0" "" "" "" "" "00183695" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183696" "" "" "" "1" "" "00008" "" "reference haplotype/ Tentative allele" "" "" "" "" "0" "" "" "" "" "00183697" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype / Tentative allele" "" "" "" "" "0" "" "" "" "" "00183698" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype / Tentative allele" "" "" "" "" "0" "" "" "" "" "00183699" "" "" "" "1" "" "00008" "" "reference haplotype/ Tentative allele" "" "" "" "" "0" "" "" "" "" "00183700" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype / Tentative allele" "" "" "" "" "0" "" "" "" "" "00183701" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype / Tentative allele" "" "" "" "" "0" "" "" "" "" "00183702" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype / Tentative allele" "" "" "" "" "0" "" "" "" "" "00183703" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183704" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183705" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2007:17522595}" "" "" "" "" "" "0" "" "" "" "" "00183706" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183707" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183708" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183709" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183710" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183711" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183712" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183713" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183714" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183715" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183716" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183717" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183718" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183719" "" "" "" "1" "" "00008" "" "reference haplotype/ (Decr.)†" "" "" "" "" "0" "" "" "" "" "00183720" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183721" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183722" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183723" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183724" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183725" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183726" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183727" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183728" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183729" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183730" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183731" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183732" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183733" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183734" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183735" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183736" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183737" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183738" "" "" "" "1" "" "00008" "" "reference haplotype/ Predicted haplotype" "" "" "" "" "0" "" "" "" "" "00183739" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183740" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183741" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183742" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183743" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183744" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183747" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183748" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183751" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183752" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183753" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183754" "" "" "" "1" "" "00008" "" "reference haplotype/ Decr. expr./Decr. activity per pmol" "" "" "" "" "0" "" "" "" "" "00183755" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183756" "" "" "" "1" "" "00008" "" "reference haplotype/ Decr. expr./Incr. activity per pmol" "" "" "" "" "0" "" "" "" "" "00183757" "" "" "" "1" "" "00008" "" "reference haplotype/ Decr. expr./Incr. activity per pmol" "" "" "" "" "0" "" "" "" "" "00183758" "" "" "" "1" "" "00008" "" "reference haplotype/ Decr. expr./Incr. activity per pmol" "" "" "" "" "0" "" "" "" "" "00183760" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, present in characterized haplotypes" "" "" "" "" "0" "" "" "" "" "00183762" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183763" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183764" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183765" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183766" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183767" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183768" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183769" "" "" "" "1" "" "00008" "" "reference haplotype/ Additional SNPs, where the haplotype has not yet been determined" "" "" "" "" "0" "" "" "" "" "00183770" "" "" "" "1" "" "00008" "{PMID:Yamano 1990:2322567}, {PMID:Nakajima 2001:11180041}, {PMID:Pitarque 2004:14974084}" "" "" "" "" "" "0" "" "" "" "" "00183771" "" "" "" "1" "" "00008" "{PMID:Oscarson 1999b:10544257}, {PMID:Ariyoshi 2000:11186131}, {PMID:Pitarque 2004:14974084}" "" "" "" "" "" "0" "" "" "" "" "00183772" "" "" "" "1" "" "00008" "{PMID:Kiyotani 2002:15618701}" "" "" "" "" "" "0" "" "" "" "" "00183773" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2010:20136358}" "" "" "" "" "" "0" "" "" "" "" "00183774" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183775" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183776" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183777" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183778" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183779" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183780" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183781" "" "" "" "1" "" "00008" "{PMID:Nakajima 2006:16952495}" "" "" "" "" "" "0" "" "" "" "" "00183782" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2007:17522595}" "" "" "" "" "" "0" "" "" "" "" "00183783" "" "" "" "1" "" "00008" "" "reference haplotype" "" "" "" "" "0" "" "" "" "" "00183784" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183785" "" "" "" "1" "" "00008" "{PMID:Pitarque 2004:14974084}" "" "" "" "" "" "0" "" "" "" "" "00183786" "" "" "" "1" "" "00008" "{PMID:Nakajima 2004:15225612}" "" "" "" "" "" "0" "" "" "" "" "00183787" "" "" "" "1" "" "00008" "{PMID:Nakajima 2004:15225612}" "" "" "" "" "" "0" "" "" "" "" "00183788" "" "" "" "1" "" "00008" "{PMID:von Richter 2004:15247629}" "" "" "" "" "" "0" "" "" "" "" "00183789" "" "" "" "1" "" "00008" "{PMID:von Richter 2004:15247629}" "" "" "" "" "" "0" "" "" "" "" "00183790" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183791" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2010:20136358}" "" "" "" "" "" "0" "" "" "" "" "00183792" "" "" "" "1" "" "00008" "{PMID:Rao 2000:10999944}" "" "" "" "" "" "0" "" "" "" "" "00183793" "" "" "" "1" "" "00008" "{PMID:Fukami 2007:17267622}" "" "" "" "" "" "0" "" "" "" "" "00183794" "" "" "" "1" "" "00008" "{PMID:Yamano 1990:2322567}, {PMID:Hadidi 1997:9409631}, {PMID:Oscarson1998:9827545}" "" "" "" "" "" "0" "" "" "" "" "00183795" "" "" "" "1" "" "00008" "{PMID:Oscarson 1999b:10544257}" "" "" "" "" "" "0" "" "" "" "" "00183796" "" "" "" "1" "" "00008" "{PMID:Kitagawa 2001:11278503}" "" "" "" "" "" "0" "" "" "" "" "00183797" "" "" "" "1" "" "00008" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "" "" "" "" "0" "" "" "" "" "00183798" "" "" "" "1" "" "00008" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "" "" "" "" "0" "" "" "" "" "00183799" "" "" "" "1" "" "00008" "{PMID:Pitarque 2001:11394901}, {PMID: Yoshida 2003:12844137}, {PMID:Kiyotani 2003:14583682}, {PMID: von Richter 2004:15247629}" "" "" "" "" "" "0" "" "" "" "" "00183800" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183801" "" "" "" "1" "" "00008" "{PMID:Yoshida 2002:12445030}, {PMID:Xu 2002:11779172}" "" "" "" "" "" "0" "" "" "" "" "00183802" "" "" "" "1" "" "00008" "{PMID:Daigo 2002:12042667}" "" "" "" "" "" "0" "" "" "" "" "00183803" "" "" "" "1" "" "00008" "{PMID:Oscarson 2002:12325023}" "" "" "" "" "" "0" "" "" "" "" "00183804" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183805" "" "" "" "1" "" "00008" "{PMID:Kiyotani 2002:15618701}" "" "" "" "" "" "0" "" "" "" "" "00183806" "" "" "" "1" "" "00008" "{PMID:Kiyotani 2002:15618701}" "" "" "" "" "" "0" "" "" "" "" "00183807" "" "" "" "1" "" "00008" "{PMID:Kiyotani 2002:15618701}" "" "" "" "" "" "0" "" "" "" "" "00183808" "" "" "" "1" "" "00008" "{PMID:Kiyotani 2002:15618701}" "" "" "" "" "" "0" "" "" "" "" "00183809" "" "" "" "1" "" "00008" "{PMID:Fukami 2004:15592323}" "" "" "" "" "" "0" "" "" "" "" "00183810" "" "" "" "1" "" "00008" "{PMID:Fukami 2005a:15900015}" "" "" "" "" "" "0" "" "" "" "" "00183811" "" "" "" "1" "" "00008" "{PMID:Fukami 2005a:15900015}" "" "" "" "" "" "0" "" "" "" "" "00183812" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183813" "" "" "" "1" "" "00008" "{PMID:Fukami 2005a:15900015}" "" "" "" "" "" "0" "" "" "" "" "00183814" "" "" "" "1" "" "00008" "{PMID:Fukami 2005b:15993850}" "" "" "" "" "" "0" "" "" "" "" "00183815" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}, {PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183816" "" "" "" "1" "" "00008" "{PMID:Haberl 2005:16041240}" "" "" "" "" "" "0" "" "" "" "" "00183817" "" "" "" "1" "" "00008" "{PMID:Ho 2008:18216723}" "" "" "" "" "" "0" "" "" "" "" "00183818" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183819" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183820" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183821" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183822" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183825" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183826" "" "" "" "1" "" "00008" "{PMID:Mwenifumbo 2008:18360915}" "" "" "" "" "" "0" "" "" "" "" "00183829" "" "" "" "1" "" "00008" "{PMID:Koudsi 2009:19365400}" "" "" "" "" "" "0" "" "" "" "" "00183830" "" "" "" "1" "" "00008" "{PMID:Bloom 2011:21597399}" "" "" "" "" "" "0" "" "" "" "" "00183831" "" "" "" "1" "" "00008" "{PMID:Piliguan 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00183832" "" "" "" "1" "" "00008" "{PMID:Piliguian 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00183833" "" "" "" "1" "" "00008" "{PMID:Piliguian 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00183834" "" "" "" "1" "" "00008" "{PMID:Piliguian 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00183835" "" "" "" "1" "" "00008" "{PMID:Piliguian 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00183836" "" "" "" "1" "" "00008" "{PMID:Piliguian 2014:24305170}" "" "" "" "" "" "0" "" "" "" "" "00292135" "" "" "" "24" "" "03575" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "analysis 2794 individuals (India)" "" "" "India" "" "0" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 17 "{{individualid}}" "{{diseaseid}}" "00183692" "04272" "00183716" "04264" "00183717" "04264" "00183719" "04264" "00183720" "00000" "00183723" "04264" "00183724" "04264" "00183725" "04264" "00183737" "04264" "00183739" "04264" "00183740" "04264" "00183751" "04264" "00183754" "04264" "00183756" "04272" "00183757" "04272" "00183758" "04272" "00292135" "00198" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00000, 00198, 00639, 01269, 01586, 04264, 04272 ## Count = 0 ## Screenings ## Do not remove or alter this header ## ## Count = 136 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000184660" "00183692" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184661" "00183693" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184662" "00183694" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184663" "00183695" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184664" "00183696" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184665" "00183697" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184666" "00183698" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184667" "00183699" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184668" "00183700" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184669" "00183701" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184670" "00183702" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184671" "00183703" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184672" "00183704" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184673" "00183705" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184674" "00183706" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184675" "00183707" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184676" "00183708" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184677" "00183709" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184678" "00183710" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184679" "00183711" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184680" "00183712" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184681" "00183713" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184682" "00183714" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184683" "00183715" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184684" "00183716" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184685" "00183717" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184686" "00183718" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184687" "00183719" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184688" "00183720" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184689" "00183721" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184690" "00183722" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184691" "00183723" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184692" "00183724" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184693" "00183725" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184694" "00183726" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184695" "00183727" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184696" "00183728" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184697" "00183729" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184698" "00183730" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184699" "00183731" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184700" "00183732" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184701" "00183733" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184702" "00183734" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184703" "00183735" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184704" "00183736" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184705" "00183737" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184706" "00183738" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184707" "00183739" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184708" "00183740" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184709" "00183741" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184710" "00183742" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184711" "00183743" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184712" "00183744" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184715" "00183747" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184716" "00183748" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184719" "00183751" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184720" "00183752" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184721" "00183753" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184722" "00183754" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184723" "00183755" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184724" "00183756" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184725" "00183757" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184726" "00183758" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184728" "00183760" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184730" "00183762" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184731" "00183763" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184732" "00183764" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184733" "00183765" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184734" "00183766" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184735" "00183767" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184736" "00183768" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184737" "00183769" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184738" "00183770" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184739" "00183771" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184740" "00183772" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184741" "00183773" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184742" "00183774" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184743" "00183775" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184744" "00183776" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184745" "00183777" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184746" "00183778" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184747" "00183779" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184748" "00183780" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184749" "00183781" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184750" "00183782" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184751" "00183783" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184752" "00183784" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184753" "00183785" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184754" "00183786" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184755" "00183787" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184756" "00183788" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184757" "00183789" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184758" "00183790" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184759" "00183791" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184760" "00183792" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184761" "00183793" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184762" "00183794" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184763" "00183795" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184764" "00183796" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184765" "00183797" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184766" "00183798" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184767" "00183799" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184768" "00183800" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184769" "00183801" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184770" "00183802" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184771" "00183803" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184772" "00183804" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184773" "00183805" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184774" "00183806" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184775" "00183807" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184776" "00183808" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184777" "00183809" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184778" "00183810" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184779" "00183811" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184780" "00183812" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184781" "00183813" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184782" "00183814" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184783" "00183815" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184784" "00183816" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184785" "00183817" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184786" "00183818" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184787" "00183819" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184788" "00183820" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184789" "00183821" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184790" "00183822" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184793" "00183825" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184794" "00183826" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184797" "00183829" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184798" "00183830" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184799" "00183831" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184800" "00183832" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184801" "00183833" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184802" "00183834" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184803" "00183835" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000184804" "00183836" "1" "00008" "00008" "2018-10-27 11:56:01" "" "" "SEQ" "DNA" "" "" "0000293303" "00292135" "1" "03575" "00006" "2020-03-11 19:30:02" "" "" "arraySNP" "DNA" "" "Infinium Global Screening Array v1.0" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 135 "{{screeningid}}" "{{geneid}}" "0000184660" "CYP2A6" "0000184661" "CYP2A6" "0000184662" "CYP2A6" "0000184663" "CYP2A6" "0000184664" "CYP2A6" "0000184665" "CYP2A6" "0000184666" "CYP2A6" "0000184667" "CYP2A6" "0000184668" "CYP2A6" "0000184669" "CYP2A6" "0000184670" "CYP2A6" "0000184671" "CYP2A6" "0000184672" "CYP2A6" "0000184673" "CYP2A6" "0000184674" "CYP2A6" "0000184675" "CYP2A6" "0000184676" "CYP2A6" "0000184677" "CYP2A6" "0000184678" "CYP2A6" "0000184679" "CYP2A6" "0000184680" "CYP2A6" "0000184681" "CYP2A6" "0000184682" "CYP2A6" "0000184683" "CYP2A6" "0000184684" "CYP2A6" "0000184685" "CYP2A6" "0000184686" "CYP2A6" "0000184687" "CYP2A6" "0000184688" "CYP2A6" "0000184689" "CYP2A6" "0000184690" "CYP2A6" "0000184691" "CYP2A6" "0000184692" "CYP2A6" "0000184693" "CYP2A6" "0000184694" "CYP2A6" "0000184695" "CYP2A6" "0000184696" "CYP2A6" "0000184697" "CYP2A6" "0000184698" "CYP2A6" "0000184699" "CYP2A6" "0000184700" "CYP2A6" "0000184701" "CYP2A6" "0000184702" "CYP2A6" "0000184703" "CYP2A6" "0000184704" "CYP2A6" "0000184705" "CYP2A6" "0000184706" "CYP2A6" "0000184707" "CYP2A6" "0000184708" "CYP2A6" "0000184709" "CYP2A6" "0000184710" "CYP2A6" "0000184711" "CYP2A6" "0000184712" "CYP2A6" "0000184715" "CYP2A6" "0000184716" "CYP2A6" "0000184719" "CYP2A6" "0000184720" "CYP2A6" "0000184721" "CYP2A6" "0000184722" "CYP2A6" "0000184723" "CYP2A6" "0000184724" "CYP2A6" "0000184725" "CYP2A6" "0000184726" "CYP2A6" "0000184728" "CYP2A6" "0000184730" "CYP2A6" "0000184731" "CYP2A6" "0000184732" "CYP2A6" "0000184733" "CYP2A6" "0000184734" "CYP2A6" "0000184735" "CYP2A6" "0000184736" "CYP2A6" "0000184737" "CYP2A6" "0000184738" "CYP2A6" "0000184739" "CYP2A6" "0000184740" "CYP2A6" "0000184741" "CYP2A6" "0000184742" "CYP2A6" "0000184743" "CYP2A6" "0000184744" "CYP2A6" "0000184745" "CYP2A6" "0000184746" "CYP2A6" "0000184747" "CYP2A6" "0000184748" "CYP2A6" "0000184749" "CYP2A6" "0000184750" "CYP2A6" "0000184751" "CYP2A6" "0000184752" "CYP2A6" "0000184753" "CYP2A6" "0000184754" "CYP2A6" "0000184755" "CYP2A6" "0000184756" "CYP2A6" "0000184757" "CYP2A6" "0000184758" "CYP2A6" "0000184759" "CYP2A6" "0000184760" "CYP2A6" "0000184761" "CYP2A6" "0000184762" "CYP2A6" "0000184763" "CYP2A6" "0000184764" "CYP2A6" "0000184765" "CYP2A6" "0000184766" "CYP2A6" "0000184767" "CYP2A6" "0000184768" "CYP2A6" "0000184769" "CYP2A6" "0000184770" "CYP2A6" "0000184771" "CYP2A6" "0000184772" "CYP2A6" "0000184773" "CYP2A6" "0000184774" "CYP2A6" "0000184775" "CYP2A6" "0000184776" "CYP2A6" "0000184777" "CYP2A6" "0000184778" "CYP2A6" "0000184779" "CYP2A6" "0000184780" "CYP2A6" "0000184781" "CYP2A6" "0000184782" "CYP2A6" "0000184783" "CYP2A6" "0000184784" "CYP2A6" "0000184785" "CYP2A6" "0000184786" "CYP2A6" "0000184787" "CYP2A6" "0000184788" "CYP2A6" "0000184789" "CYP2A6" "0000184790" "CYP2A6" "0000184793" "CYP2A6" "0000184794" "CYP2A6" "0000184797" "CYP2A6" "0000184798" "CYP2A6" "0000184799" "CYP2A6" "0000184800" "CYP2A6" "0000184801" "CYP2A6" "0000184802" "CYP2A6" "0000184803" "CYP2A6" "0000184804" "CYP2A6" ## Variants_On_Genome ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 820 "{{id}}" "{{allele}}" "{{effectid}}" "{{chromosome}}" "{{position_g_start}}" "{{position_g_end}}" "{{type}}" "{{average_frequency}}" "{{owned_by}}" "{{VariantOnGenome/DBID}}" "{{VariantOnGenome/DNA}}" "{{VariantOnGenome/Frequency}}" "{{VariantOnGenome/Reference}}" "{{VariantOnGenome/Restriction_site}}" "{{VariantOnGenome/Published_as}}" "{{VariantOnGenome/Remarks}}" "{{VariantOnGenome/Genetic_origin}}" "{{VariantOnGenome/Segregation}}" "{{VariantOnGenome/dbSNP}}" "{{VariantOnGenome/VIP}}" "{{VariantOnGenome/Methylation}}" "{{VariantOnGenome/ISCN}}" "{{VariantOnGenome/DNA/hg38}}" "{{VariantOnGenome/ClinVar}}" "{{VariantOnGenome/ClinicalClassification}}" "{{VariantOnGenome/ClinicalClassification/Method}}" "0000248764" "0" "10" "19" "41350664" "41350664" "subst" "0.987409" "02325" "CYP2A6_000002" "g.41350664A>T" "" "" "" "CYP2A6(NM_000762.6):c.1175T>A (p.F392Y)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.40844759=" "" "benign" "" "0000254697" "0" "30" "19" "41355849" "41355849" "subst" "0" "01943" "CYP2A6_000004" "g.41355849A>G" "" "" "" "CYP2A6(NM_000762.5):c.217T>C (p.L73=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.40849944A>G" "" "likely benign" "" "0000254791" "0" "30" "19" "41352825" "41352825" "subst" "1.21981E-5" "01943" "CYP2A6_000003" "g.41352825A>G" "" "" "" "CYP2A6(NM_000762.5):c.786T>C (p.N262=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.40846920A>G" "" "likely benign" "" "0000267254" "0" "10" "19" "41356281" "41356281" "subst" "0.755578" "02325" "CYP2A6_000005" "g.41356281T>C" "" "" "" "CYP2A6(NM_000762.6):c.51A>G (p.V17=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.40850376T>C" "" "benign" "" "0000408785" "1" "99" "19" "41349626" "4294967295" "" "0" "00008" "CYP2A6_000006" "g.(41349626_?)con?" "" "{PMID:Yamano 1990:2322567}, {PMID:Nakajima 2001:11180041}, {PMID:Pitarque 2004:14974084}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "pathogenic" "" "0000408786" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Oscarson 1999b:10544257}, {PMID:Ariyoshi 2000:11186131}, {PMID:Pitarque 2004:14974084}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408787" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Oscarson 1999b:10544257}, {PMID:Ariyoshi 2000:11186131}, {PMID:Pitarque 2004:14974084}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408788" "1" "33" "19" "41356727" "41356727" "subst" "0" "00008" "CYP2A6_000162" "g.41356727C>T" "" "{PMID:Kiyotani 2002:15618701}" "" "-395G>A" "" "Germline" "" "" "0" "" "" "g.40850822C>T" "" "likely benign" "" "0000408789" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Kiyotani 2002:15618701}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408790" "1" "33" "19" "41349250" "41349259" "" "0" "00008" "CYP2A6_000008" "g.41349250_41349259con?" "" "{PMID:Mwenifumbo 2010:20136358}" "" "gene conversion at 7073-7082" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408791" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Mwenifumbo 2010:20136358}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408792" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408793" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408794" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408795" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408796" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408797" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408798" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408799" "1" "33" "19" "41355068" "41355068" "subst" "0" "00008" "CYP2A6_000133" "g.41355068G>C" "" "{PMID:Haberl 2005:16041240}" "" "6285A>G" "" "Germline" "" "" "0" "" "" "g.40849163G>C" "" "likely benign" "" "0000408800" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408801" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408802" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408803" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408804" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408805" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408806" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "{PMID:Haberl 2005:16041240}" "" "6293T>C" "" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000408807" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408808" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408809" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408810" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "{PMID:Haberl 2005:16041240}" "" "-1464A>T" "" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000408811" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408812" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408813" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408814" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408815" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408816" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408817" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408818" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "{PMID:Haberl 2005:16041240}" "" "-1464A>T" "" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000408819" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408820" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408821" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408822" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408823" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408824" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408825" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408826" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "{PMID:Haberl 2005:16041240}" "" "-1464A>T" "" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000408827" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408828" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408829" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408830" "1" "33" "19" "41349943" "41349943" "subst" "0" "00008" "CYP2A6_000034" "g.41349943G>C" "" "{PMID:Haberl 2005:16041240}" "" "6389C>G" "" "Germline" "" "" "0" "" "" "g.40844038G>C" "" "likely benign" "" "0000408831" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408832" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408833" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408834" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408835" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "{PMID:Haberl 2005:16041240}" "" "-1464A>T" "" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000408836" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408837" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408838" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408839" "1" "33" "19" "41350704" "41350704" "subst" "0.000777281" "00008" "CYP2A6_000060" "g.41350704G>A" "" "{PMID:Haberl 2005:16041240}" "" "5628C>T" "" "Germline" "" "" "0" "" "" "g.40844799G>A" "" "likely benign" "" "0000408840" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408841" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Haberl 2005:16041240}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408842" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Haberl 2005:16041240}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408843" "1" "33" "19" "41349641" "41349641" "subst" "0" "00008" "CYP2A6_000022" "g.41349641G>C" "" "{PMID:Nakajima 2006:16952495}" "" "1545C>G" "" "Germline" "" "" "0" "" "" "g.40843736G>C" "" "likely benign" "" "0000408844" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Nakajima 2006:16952495}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000408845" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Nakajima 2006:16952495}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408846" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "{PMID:Nakajima 2006:16952495}" "" "22C>T" "" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000408847" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "1636C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000408848" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000408849" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Mwenifumbo 2007:17522595}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408850" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000408851" "1" "33" "19" "41355994" "41355994" "subst" "0" "00008" "CYP2A6_000150" "g.41355994A>G" "" "{PMID:Mwenifumbo 2007:17522595}" "" "338T>C" "" "Germline" "" "" "0" "" "" "g.40850089A>G" "" "likely benign" "" "0000408852" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Mwenifumbo 2007:17522595}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408853" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "1636C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000408854" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Mwenifumbo 2007:17522595}" "" "1191T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000408855" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2007:17522595}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408856" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2007:17522595}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408857" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000408858" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000408859" "1" "33" "19" "41349372" "41349373" "ins" "0" "00008" "CYP2A6_000014" "g.41349372_41349373insTTTTCC" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 6960_6961insGAAAAG" "" "Germline" "" "" "0" "" "" "g.40843467_40843468insTTTTCC" "" "likely benign" "" "0000408860" "1" "33" "19" "41349343" "41349343" "subst" "0" "00008" "CYP2A6_000013" "g.41349343T>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 6989A>G" "" "Germline" "" "" "0" "" "" "g.40843438T>C" "" "likely benign" "" "0000408861" "1" "33" "19" "41349323" "41349324" "delins" "0" "00008" "CYP2A6_000012" "g.41349323_41349324delinsTAGAGC" "" "{PMID:Mwenifumbo 2007:17522595}" "" "3\' CYP2A7 conversion 7008_7009TC>GCTCTA" "" "Germline" "" "" "0" "" "" "g.40843418_40843419delinsTAGAGC" "" "likely benign" "" "0000408863" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2007:17522595}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000408864" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "{PMID:Mwenifumbo 2007:17522595}" "" "22C>T" "" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000408865" "1" "33" "19" "41354702" "41354702" "subst" "0.00300286" "00008" "CYP2A6_000130" "g.41354702A>G" "" "{PMID:Mwenifumbo 2007:17522595}" "" "1630T>C" "" "Germline" "" "" "0" "" "" "g.40848797A>G" "" "likely benign" "" "0000408866" "1" "33" "19" "41351355" "41351355" "subst" "6.0987E-5" "00008" "CYP2A6_000072" "g.41351355G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1005C>T" "" "Germline" "" "" "0" "" "" "g.40845450G>A" "" "likely benign" "" "0000408867" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6782C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000408868" "1" "33" "19" "41349500" "41349500" "subst" "0" "00008" "CYP2A6_000018" "g.41349500T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6832A>G" "" "Germline" "" "" "0" "" "" "g.40843595T>C" "" "likely benign" "" "0000408869" "1" "33" "19" "41349497" "41349497" "subst" "0" "00008" "CYP2A6_000017" "g.41349497G>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6835C>A" "" "Germline" "" "" "0" "" "" "g.40843592G>T" "" "likely benign" "" "0000408870" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000408871" "1" "33" "19" "41349372" "41349373" "ins" "0" "00008" "CYP2A6_000014" "g.41349372_41349373insTTTTCC" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6960_6961insGAAAAG" "" "Germline" "" "" "0" "" "" "g.40843467_40843468insTTTTCC" "" "likely benign" "" "0000408872" "1" "33" "19" "41349343" "41349343" "subst" "0" "00008" "CYP2A6_000013" "g.41349343T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6989A>G" "" "Germline" "" "" "0" "" "" "g.40843438T>C" "" "likely benign" "" "0000408874" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000408875" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408876" "1" "33" "19" "41350189" "41350189" "subst" "0" "00008" "CYP2A6_000041" "g.41350189G>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6143C>A" "" "Germline" "" "" "0" "" "" "g.40844284G>T" "" "likely benign" "" "0000408877" "1" "33" "19" "41354686" "41354686" "subst" "0" "00008" "CYP2A6_000129" "g.41354686G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1646C>T" "" "Germline" "" "" "0" "" "" "g.40848781G>A" "" "likely benign" "" "0000408878" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408879" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408880" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000408881" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2296C>T" "" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000408882" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000408883" "1" "33" "19" "41352544" "41352544" "subst" "0" "00008" "CYP2A6_000087" "g.41352544G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3788C>T" "" "Germline" "" "" "0" "" "" "g.40846639G>A" "" "likely benign" "" "0000408884" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4071delA" "" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000408885" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4636A>C" "" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000408886" "1" "33" "19" "41351482" "41351482" "subst" "0" "00008" "CYP2A6_000075" "g.41351482G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4850C>T" "" "Germline" "" "" "0" "" "" "g.40845577G>A" "" "likely benign" "" "0000408887" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Pitarque 2004:14974084}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408888" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "{PMID:Nakajima 2004:15225612}" "" "1224C>T" "" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000408889" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "{PMID:Nakajima 2004:15225612}" "" "1224C>T" "" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000408890" "1" "33" "19" "41350507" "41350507" "subst" "0.0110735" "00008" "CYP2A6_000044" "g.41350507T>C" "" "{PMID:Nakajima 2004:15225612}" "" "5825A>G" "" "Germline" "" "" "0" "" "" "g.40844602T>C" "" "likely benign" "" "0000408891" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:von Richter 2004:15247629}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000408892" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:von Richter 2004:15247629}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408893" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:von Richter 2004:15247629}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000408894" "1" "33" "19" "41357530" "41357531" "ins" "0" "00008" "CYP2A6_000170" "g.41357530_41357531insN[316]" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1199_-1198ins316bpAlu" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408895" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408896" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408897" "1" "33" "19" "41357018" "41357018" "subst" "0" "00008" "CYP2A6_000164" "g.41357018T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-686A>G" "" "Germline" "" "" "0" "" "" "g.40851113T>C" "" "likely benign" "" "0000408898" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000408899" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408900" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000408901" "1" "33" "19" "41355901" "41355901" "subst" "0.00014733" "00008" "CYP2A6_000147" "g.41355901G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "431C>T" "" "Germline" "" "" "0" "" "" "g.40849996G>A" "" "likely benign" "" "0000408902" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "459G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000408903" "1" "33" "19" "41352954" "41352954" "subst" "0" "00008" "CYP2A6_000094" "g.41352954G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "657C>T" "" "Germline" "" "" "0" "" "" "g.40847049G>A" "" "likely benign" "" "0000408904" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408905" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1779G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000408906" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408907" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000408908" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000408909" "1" "33" "19" "41352954" "41352954" "subst" "0" "00008" "CYP2A6_000094" "g.41352954G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3378C>T" "" "Germline" "" "" "0" "" "" "g.40847049G>A" "" "likely benign" "" "0000408910" "1" "33" "19" "41352428" "41352428" "subst" "0" "00008" "CYP2A6_000085" "g.41352428C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3904G>A" "" "Germline" "" "" "0" "" "" "g.40846523C>T" "" "likely benign" "" "0000408911" "1" "33" "19" "41352268" "41352268" "del" "0" "00008" "CYP2A6_000084" "g.41352268del" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4074delA" "" "Germline" "" "" "0" "" "" "g.40846363del" "" "likely benign" "" "0000408912" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Mwenifumbo 2010:20136358}" "" "gene conversion at 7073-7082" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408913" "1" "33" "19" "41349443" "41356352" "dup" "0" "00008" "CYP2A6_000016" "g.(?_41349443)_(41356352_?)dup" "" "{PMID:Rao 2000:10999944}" "" "c.(?_-21)_(*258_?)dup" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408914" "1" "33" "19" "41349443" "41356352" "dup" "0" "00008" "CYP2A6_000016" "g.(?_41349443)_(41356352_?)dup" "" "{PMID:Fukami 2007:17267622}" "" "c.(?_-21)_(*258_?)dup" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408915" "1" "99" "19" "41354533" "41354533" "subst" "0.0197392" "00008" "CYP2A6_000119" "g.41354533A>T" "" "{PMID:Yamano 1990:2322567}, {PMID:Hadidi 1997:9409631}, {PMID:Oscarson1998:9827545}" "" "479T>A" "" "Germline" "" "rs1801272" "0" "" "" "g.40848628A>T" "" "pathogenic" "" "0000408916" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Yamano 1990:2322567}, {PMID:Hadidi 1997:9409631}, {PMID:Oscarson1998:9827545}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408917" "1" "99" "19" "41349750" "41349750" "subst" "0" "00008" "CYP2A6_000029" "g.41349750C>A" "" "{PMID:Oscarson 1999b:10544257}" "" "1436G>T" "" "Germline" "" "rs5031017" "0" "" "" "g.40843845C>A" "" "pathogenic" "" "0000408918" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Oscarson 1999b:10544257}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408919" "1" "33" "19" "41354629" "41354629" "subst" "2.85717E-5" "00008" "CYP2A6_000126" "g.41354629C>T" "" "{PMID:Kitagawa 2001:11278503}" "" "383G>A" "" "Germline" "" "" "0" "" "" "g.40848724C>T" "" "likely benign" "" "0000408920" "1" "99" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "1412T>C" "" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "pathogenic" "" "0000408921" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408922" "1" "11" "19" "41349732" "41349732" "subst" "0.00164576" "00008" "CYP2A6_000027" "g.41349732C>A" "" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "1454G>T" "" "Germline" "" "rs28399468" "0" "" "" "g.40843827C>A" "" "benign" "" "0000408923" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Ariyoshi 2001:11237731}, {PMID:Xu 2002:11779172}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408924" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Pitarque 2001:11394901}, {PMID: Yoshida 2003:12844137}, {PMID:Kiyotani 2003:14583682}, {PMID: von Richter 2004:15247629}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408925" "1" "99" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "{PMID:Pitarque 2001:11394901}, {PMID: Yoshida 2003:12844137}, {PMID:Kiyotani 2003:14583682}, {PMID: von Richter 2004:15247629}" "" "-48T>G" "" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "pathogenic" "" "0000408926" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Haberl 2005:16041240}" "" "1547C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000408927" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408928" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408929" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408930" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408931" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "{PMID:Haberl 2005:16041240}" "" "-48T>G" "" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000408932" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Haberl 2005:16041240}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000408933" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408934" "1" "33" "19" "41354496" "41354496" "subst" "0.0793229" "00008" "CYP2A6_000118" "g.41354496C>A" "" "{PMID:Haberl 2005:16041240}" "" "1836G>T" "" "Germline" "" "" "0" "" "" "g.40848591C>A" "" "likely benign" "" "0000408935" "1" "99" "19" "41349732" "41349732" "subst" "0.00164576" "00008" "CYP2A6_000027" "g.41349732C>A" "" "{PMID:Yoshida 2002:12445030}, {PMID:Xu 2002:11779172}" "" "1454G>T" "" "Germline" "" "rs28399468" "0" "" "" "g.40843827C>A" "" "pathogenic" "" "0000408936" "1" "99" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "{PMID:Yoshida 2002:12445030}, {PMID:Xu 2002:11779172}" "" "1412T>C" "" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "pathogenic" "" "0000408937" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Yoshida 2002:12445030}, {PMID:Xu 2002:11779172}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408938" "1" "99" "19" "41352941" "41352941" "subst" "0.00103497" "00008" "CYP2A6_000093" "g.41352941A>G" "" "{PMID:Daigo 2002:12042667}" "" "670T>C" "" "Germline" "" "rs28399447" "0" "" "" "g.40847036A>G" "" "pathogenic" "" "0000408939" "1" "99" "19" "41349443" "41354669" "" "0" "00008" "CYP2A6_000009" "g.(?_41349443)_(41354669_41355722)con(?_41388657)_(41386150_41386383)" "" "{PMID:Oscarson 2002:12325023}" "" "exons1-2ofCYP2A7origin" "" "Germline" "" "" "0" "" "" "" "" "pathogenic" "" "0000408940" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Haberl 2005:16041240}" "" "1547C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000408941" "1" "33" "19" "41351169" "41351169" "subst" "0.0301293" "00008" "CYP2A6_000067" "g.41351169C>T" "" "{PMID:Haberl 2005:16041240}" "" "5163G>A" "" "Germline" "" "" "0" "" "" "g.40845264C>T" "" "likely benign" "" "0000408942" "1" "33" "19" "41350787" "41350787" "subst" "0" "00008" "CYP2A6_000062" "g.41350787C>G" "" "{PMID:Haberl 2005:16041240}" "" "5545G>C" "" "Germline" "" "" "0" "" "" "g.40844882C>G" "" "likely benign" "" "0000408943" "1" "33" "19" "41350615" "41350615" "subst" "0" "00008" "CYP2A6_000052" "g.41350615G>C" "" "{PMID:Haberl 2005:16041240}" "" "5717C>G" "" "Germline" "" "" "0" "" "" "g.40844710G>C" "" "likely benign" "" "0000408944" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408945" "1" "33" "19" "41352936" "41352936" "subst" "0.0187923" "00008" "CYP2A6_000092" "g.41352936C>T" "" "{PMID:Haberl 2005:16041240}" "" "3396G>A" "" "Germline" "" "" "0" "" "" "g.40847031C>T" "" "likely benign" "" "0000408946" "1" "33" "19" "41351843" "41351843" "subst" "0.0299024" "00008" "CYP2A6_000079" "g.41351843G>A" "" "{PMID:Haberl 2005:16041240}" "" "4489C>T" "" "Germline" "" "" "0" "" "" "g.40845938G>A" "" "likely benign" "" "0000408947" "1" "33" "19" "41349443" "41354669" "" "0" "00008" "CYP2A6_000009" "g.(?_41349443)_(41354669_41355722)con(?_41388657)_(41386150_41386383)" "" "{PMID:Haberl 2005:16041240}" "" "exons1-2ofCYP2A7origin" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408948" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "{PMID:Kiyotani 2002:15618701}" "" "-48T>G" "" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000408949" "1" "33" "19" "41356319" "41356319" "subst" "3.2719E-5" "00008" "CYP2A6_000160" "g.41356319C>T" "" "{PMID:Kiyotani 2002:15618701}" "" "13G>A" "" "Germline" "" "rs28399434" "0" "" "" "g.40850414C>T" "" "likely benign" "" "0000408950" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Kiyotani 2002:15618701}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408951" "1" "33" "19" "41356246" "41356246" "subst" "0.0286566" "00008" "CYP2A6_000155" "g.41356246C>T" "" "{PMID:Kiyotani 2002:15618701}" "" "86G>A" "" "Germline" "" "rs28399435" "0" "" "" "g.40850341C>T" "" "likely benign" "" "0000408952" "1" "33" "19" "41354198" "41354198" "subst" "0.000577358" "00008" "CYP2A6_000111" "g.41354198T>C" "" "{PMID:Kiyotani 2002:15618701}" "" "580A>G" "" "Germline" "" "" "0" "" "" "g.40848293T>C" "" "likely benign" "" "0000408953" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "{PMID:Kiyotani 2002:15618701}" "" "-48T>G" "" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000408954" "1" "33" "19" "41354171" "41354171" "subst" "0.00010978" "00008" "CYP2A6_000107" "g.41354171G>T" "" "{PMID:Kiyotani 2002:15618701}" "" "607C>A" "" "Germline" "" "rs56256500" "0" "" "" "g.40848266G>T" "" "likely benign" "" "0000408955" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "{PMID:Fukami 2004:15592323}" "" "1224C>T" "" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000408956" "1" "99" "19" "41351267" "41351267" "subst" "0.00798878" "00008" "CYP2A6_000070" "g.41351267C>T" "" "{PMID:Fukami 2004:15592323}" "" "1093G>A" "" "Germline" "" "rs28399454" "0" "" "" "g.40845362C>T" "" "pathogenic" "" "0000408957" "1" "33" "19" "41351169" "41351169" "subst" "0.0301293" "00008" "CYP2A6_000067" "g.41351169C>T" "" "{PMID:Fukami 2004:15592323}" "" "5163G>A" "" "Germline" "" "" "0" "" "" "g.40845264C>T" "" "likely benign" "" "0000408958" "1" "33" "19" "41350507" "41350507" "subst" "0.0110735" "00008" "CYP2A6_000044" "g.41350507T>C" "" "{PMID:Fukami 2004:15592323}" "" "5825A>G" "" "Germline" "" "" "0" "" "" "g.40844602T>C" "" "likely benign" "" "0000408959" "1" "33" "19" "41356123" "41356123" "subst" "0.0114568" "00008" "CYP2A6_000152" "g.41356123G>A" "" "{PMID:Fukami 2004:15592323}" "" "209C>T" "" "Germline" "" "" "0" "" "" "g.40850218G>A" "" "likely benign" "" "0000408960" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Fukami 2004:15592323}" "" "459G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000408961" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Fukami 2004:15592323}" "" "1779G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000408962" "1" "33" "19" "41351843" "41351843" "subst" "0.0299024" "00008" "CYP2A6_000079" "g.41351843G>A" "" "{PMID:Fukami 2004:15592323}" "" "4489C>T" "" "Germline" "" "" "0" "" "" "g.40845938G>A" "" "likely benign" "" "0000408963" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "{PMID:Fukami 2005a:15900015}" "" "1175A>T" "Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000408964" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "{PMID:Fukami 2005a:15900015}" "" "1175A>T" "Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000408965" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Fukami 2005a:15900015}" "" "1191T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000408966" "1" "33" "19" "41350630" "41350630" "subst" "0.00513267" "00008" "CYP2A6_000053" "g.41350630A>G" "" "{PMID:Fukami 2005a:15900015}" "" "1209T>C" "" "Germline" "" "" "0" "" "" "g.40844725A>G" "" "likely benign" "" "0000408967" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Fukami 2005a:15900015}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408968" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "{PMID:Haberl 2005:16041240}" "" "1175A>T" "Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000408969" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Haberl 2005:16041240}" "" "1546C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000408970" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408971" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408972" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Haberl 2005:16041240}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408973" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "{PMID:Haberl 2005:16041240}" "" "-1464A>T" "" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000408974" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1579T>C" "" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000408975" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "{PMID:Haberl 2005:16041240}" "" "-1680A>G" "" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000408976" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Haberl 2005:16041240}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000408977" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "{PMID:Fukami 2005a:15900015}" "" "1175A>T" "Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000408978" "1" "33" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "{PMID:Fukami 2005a:15900015}" "" "1412T>C" "" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "likely benign" "" "0000408979" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Fukami 2005a:15900015}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000408980" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Fukami 2005a:15900015}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000408981" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Fukami 2005b:15993850}" "" "1191T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000408982" "1" "99" "19" "41354191" "41354192" "del" "0" "00008" "CYP2A6_000110" "g.41354191_41354192del" "" "{PMID:Fukami 2005b:15993850}" "" "587_588del" "" "Germline" "" "" "0" "" "" "g.40848286_40848287del" "" "pathogenic" "" "0000408983" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Fukami 2005b:15993850}" "" "1546C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000408984" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Fukami 2005b:15993850}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408985" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "{PMID:Fukami 2005b:15993850}" "" "2296C>T" "" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000408986" "1" "99" "19" "41349759" "41349759" "subst" "0.0123454" "00008" "CYP2A6_000030" "g.41349759T>C" "" "{PMID:Haberl 2005:16041240}, {PMID:Mwenifumbo 2008:18360915}" "" "1427A>G" "" "Germline" "" "rs6413474" "0" "" "" "g.40843854T>C" "" "pathogenic" "" "0000408987" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Haberl 2005:16041240}, {PMID:Mwenifumbo 2008:18360915}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408988" "1" "33" "19" "41354538" "41354538" "subst" "0.000655264" "00008" "CYP2A6_000121" "g.41354538G>C" "" "{PMID:Haberl 2005:16041240}" "" "474C>G" "" "Germline" "" "rs60605885" "0" "" "" "g.40848633G>C" "" "likely benign" "" "0000408989" "1" "33" "19" "41354534" "41354534" "subst" "0" "00008" "CYP2A6_000120" "g.41354534G>T" "" "{PMID:Haberl 2005:16041240}" "" "478C>A" "" "Germline" "" "rs60563539" "0" "" "" "g.40848629G>T" "" "likely benign" "" "0000408990" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Haberl 2005:16041240}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000408991" "1" "99" "19" "41354171" "41354171" "subst" "0.00106121" "00008" "CYP2A6_000108" "g.41354171G>A" "" "{PMID:Ho 2008:18216723}" "" "607C>T" "" "Germline" "" "" "0" "" "" "g.40848266G>A" "" "pathogenic" "" "0000408992" "1" "99" "19" "41349874" "41349874" "subst" "0" "00008" "CYP2A6_000032" "g.41349874T>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1312A>T" "" "Germline" "" "rs143731390" "0" "" "" "g.40843969T>A" "" "pathogenic" "" "0000408993" "1" "99" "19" "41355738" "41355738" "subst" "0.000735986" "00008" "CYP2A6_000140" "g.41355738C>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "328G>C" "" "Germline" "" "rs72549435" "0" "" "" "g.40849833C>G" "" "pathogenic" "" "0000408994" "1" "33" "19" "41355754" "41355754" "subst" "0.00106515" "00008" "CYP2A6_000141" "g.41355754T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "312A>G" "" "Germline" "" "" "0" "" "" "g.40849849T>C" "" "likely benign" "" "0000408995" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000408996" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000408997" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000408998" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6782C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000408999" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Mwenifumbo 2008:18360915}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409000" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409001" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6293T>C" "" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000409002" "1" "33" "19" "41350050" "41350050" "subst" "0" "00008" "CYP2A6_000039" "g.41350050T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6282A>G" "" "Germline" "" "" "0" "" "" "g.40844145T>C" "" "likely benign" "" "0000409003" "1" "33" "19" "41350114" "41350114" "subst" "0" "00008" "CYP2A6_000040" "g.41350114T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6218A>G" "" "Germline" "" "" "0" "" "" "g.40844209T>C" "" "likely benign" "" "0000409004" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409005" "1" "33" "19" "41355612" "41355612" "subst" "0" "00008" "CYP2A6_000137" "g.41355612C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "720G>A" "" "Germline" "" "" "0" "" "" "g.40849707C>T" "" "likely benign" "" "0000409006" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409007" "1" "33" "19" "41355195" "41355195" "subst" "0" "00008" "CYP2A6_000135" "g.41355195G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1137C>G" "" "Germline" "" "" "0" "" "" "g.40849290G>C" "" "likely benign" "" "0000409008" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409009" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409010" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3225A>G" "" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409011" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1440T>C" "" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409012" "1" "33" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "352T>C" "" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "likely benign" "" "0000409013" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409014" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409015" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409016" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409017" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6692C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409018" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409019" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "22C>T" "" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409020" "1" "33" "19" "41355564" "41355564" "subst" "0" "00008" "CYP2A6_000136" "g.41355564T>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "768A>T" "" "Germline" "" "" "0" "" "" "g.40849659T>A" "" "likely benign" "" "0000409021" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409022" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409023" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409024" "1" "33" "19" "41353727" "41353727" "subst" "0" "00008" "CYP2A6_000102" "g.41353727C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2605G>A" "" "Germline" "" "" "0" "" "" "g.40847822C>T" "" "likely benign" "" "0000409025" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2296C>T" "" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409026" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409027" "1" "33" "19" "41353411" "41353411" "subst" "0" "00008" "CYP2A6_000100" "g.41353411C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2921G>A" "" "Germline" "" "" "0" "" "" "g.40847506C>T" "" "likely benign" "" "0000409028" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4636A>C" "" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409029" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1440T>C" "" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409030" "1" "99" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "352T>C" "" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "pathogenic" "" "0000409031" "1" "99" "19" "41354629" "41354629" "subst" "0.00026939" "00008" "CYP2A6_000127" "g.41354629C>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "383G>T" "" "Germline" "" "rs4986891" "0" "" "" "g.40848724C>A" "" "pathogenic" "" "0000409032" "1" "33" "19" "41354622" "41354622" "subst" "0.000256983" "00008" "CYP2A6_000125" "g.41354622G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "390C>T" "" "Germline" "" "" "0" "" "" "g.40848717G>A" "" "likely benign" "" "0000409033" "1" "99" "19" "41354621" "41354621" "subst" "0.000256942" "00008" "CYP2A6_000124" "g.41354621A>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "391T>G" "" "Germline" "" "rs59552350" "0" "" "" "g.40848716A>C" "" "pathogenic" "" "0000409034" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409035" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409036" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409037" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409038" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "22C>T" "" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409039" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409040" "1" "33" "19" "41355167" "41355167" "subst" "0" "00008" "CYP2A6_000134" "g.41355167C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1165G>A" "" "Germline" "" "" "0" "" "" "g.40849262C>T" "" "likely benign" "" "0000409041" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409042" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409043" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2296C>T" "" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409044" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409045" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4071delA" "" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409046" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4636A>C" "" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409047" "1" "33" "19" "41354169" "41354170" "delins" "0" "00008" "CYP2A6_000106" "g.41354169_41354170delinsT" "" "{PMID:Mwenifumbo 2008:18360915}" "" "608_609GC>A" "" "Germline" "" "rs28399445" "0" "" "" "g.40848264_40848265delinsT" "" "likely benign" "" "0000409048" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1440T>C" "" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409049" "1" "33" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "352T>C" "" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "likely benign" "" "0000409050" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409051" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409052" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409053" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409054" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6692C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409055" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409056" "1" "33" "19" "41350475" "41350475" "subst" "0" "00008" "CYP2A6_000042" "g.41350475A>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5857T>A" "" "Germline" "" "" "0" "" "" "g.40844570A>T" "" "likely benign" "" "0000409057" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "22C>T" "" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409058" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409059" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409060" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409061" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2296C>T" "" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409062" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409063" "1" "33" "19" "41352460" "41352460" "subst" "0" "00008" "CYP2A6_000086" "g.41352460C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3872G>A" "" "Germline" "" "" "0" "" "" "g.40846555C>T" "" "likely benign" "" "0000409064" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4071delA" "" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409065" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4636A>C" "" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409066" "1" "33" "19" "41350587" "41350587" "subst" "0.000953359" "00008" "CYP2A6_000047" "g.41350587T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1252A>G" "" "Germline" "" "rs28399463" "0" "" "" "g.40844682T>C" "" "likely benign" "" "0000409067" "1" "33" "19" "41350582" "41350582" "subst" "0.000810789" "00008" "CYP2A6_000046" "g.41350582C>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1257G>C" "" "Germline" "" "rs8192730" "0" "" "" "g.40844677C>G" "" "likely benign" "" "0000409068" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1245C>T" "" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409069" "1" "33" "19" "41357600" "41357600" "subst" "0" "00008" "CYP2A6_000171" "g.41357600A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1269T>C" "" "Germline" "" "" "0" "" "" "g.40851695A>G" "" "likely benign" "" "0000409070" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 6782C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409071" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Mwenifumbo 2008:18360915}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409072" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3\' CYP2A7 conversion 7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409073" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409074" "1" "33" "19" "41349942" "41349942" "subst" "0" "00008" "CYP2A6_000033" "g.41349942A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6390T>C" "" "Germline" "" "" "0" "" "" "g.40844037A>G" "" "likely benign" "" "0000409075" "1" "33" "19" "41349943" "41349943" "subst" "0" "00008" "CYP2A6_000034" "g.41349943G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6389C>G" "" "Germline" "" "" "0" "" "" "g.40844038G>C" "" "likely benign" "" "0000409076" "1" "33" "19" "41349947" "41349947" "subst" "0" "00008" "CYP2A6_000035" "g.41349947C>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6385G>T" "" "Germline" "" "" "0" "" "" "g.40844042C>A" "" "likely benign" "" "0000409077" "1" "33" "19" "41349971" "41349971" "subst" "0" "00008" "CYP2A6_000036" "g.41349971G>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6361C>A" "" "Germline" "" "" "0" "" "" "g.40844066G>T" "" "likely benign" "" "0000409078" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409079" "1" "33" "19" "41355676" "41355676" "subst" "0.00172034" "00008" "CYP2A6_000138" "g.41355676C>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "656G>T" "" "Germline" "" "" "0" "" "" "g.40849771C>A" "" "likely benign" "" "0000409080" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409081" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409082" "1" "33" "19" "41351651" "41351651" "subst" "0" "00008" "CYP2A6_000076" "g.41351651A>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4681T>G" "" "Germline" "" "" "0" "" "" "g.40845746A>C" "" "likely benign" "" "0000409083" "1" "33" "19" "41353077" "41353077" "subst" "0" "00008" "CYP2A6_000097" "g.41353077T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3255A>G" "" "Germline" "" "" "0" "" "" "g.40847172T>C" "" "likely benign" "" "0000409084" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409085" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409086" "1" "33" "19" "41356801" "41356823" "delins" "0" "00008" "CYP2A6_000163" "g.41356801_41356823delinsCAGATTCCACATATGGATT" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-492_-470delCCCCTTCCTGAGACCCTTAACCCinsAATCCATATGTGGAATCTG" "" "Germline" "" "" "0" "" "" "g.40850896_40850918delinsCAGATTCCACATATGGATT" "" "likely benign" "" "0000409087" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409088" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6692C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409089" "1" "33" "19" "41348764" "41348764" "subst" "0" "00008" "CYP2A6_000010" "g.41348764G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7568C>T" "" "Germline" "" "" "0" "" "" "g.40842859G>A" "" "likely benign" "" "0000409090" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409091" "1" "33" "19" "41356316" "41356316" "subst" "0.00107459" "00008" "CYP2A6_000159" "g.41356316T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "16A>C" "" "Germline" "" "rs72549432" "0" "" "" "g.40850411T>G" "" "likely benign" "" "0000409092" "1" "33" "19" "41354993" "41354993" "subst" "0" "00008" "CYP2A6_000132" "g.41354993G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1339C>G" "" "Germline" "" "" "0" "" "" "g.40849088G>C" "" "likely benign" "" "0000409093" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409094" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409095" "1" "33" "19" "41353611" "41353611" "subst" "0" "00008" "CYP2A6_000101" "g.41353611C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2721G>A" "" "Germline" "" "" "0" "" "" "g.40847706C>T" "" "likely benign" "" "0000409096" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409097" "1" "33" "19" "41353017" "41353017" "subst" "0" "00008" "CYP2A6_000096" "g.41353017G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3315C>T" "" "Germline" "" "" "0" "" "" "g.40847112G>A" "" "likely benign" "" "0000409098" "1" "33" "19" "41355865" "41355865" "subst" "0.00100678" "00008" "CYP2A6_000146" "g.41355865G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "201C>T" "" "Germline" "" "" "0" "" "" "g.40849960G>A" "" "likely benign" "" "0000409099" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409100" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409101" "1" "33" "19" "41356801" "41356823" "delins" "0" "00008" "CYP2A6_000163" "g.41356801_41356823delinsCAGATTCCACATATGGATT" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-492_-470delCCCCTTCCTGAGACCCTTAACCCinsAATCCATATGTGGAATCTG" "" "Germline" "" "" "0" "" "" "g.40850896_40850918delinsCAGATTCCACATATGGATT" "" "likely benign" "" "0000409102" "1" "33" "19" "41357306" "41357306" "subst" "0" "00008" "CYP2A6_000166" "g.41357306A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "-975T>C" "" "Germline" "" "" "0" "" "" "g.40851401A>G" "" "likely benign" "" "0000409103" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409104" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "6692C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409105" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "5668A" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409106" "1" "33" "19" "41356316" "41356316" "subst" "0.00107459" "00008" "CYP2A6_000159" "g.41356316T>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "16A>C" "" "Germline" "" "rs72549432" "0" "" "" "g.40850411T>G" "" "likely benign" "" "0000409107" "1" "33" "19" "41354993" "41354993" "subst" "0" "00008" "CYP2A6_000132" "g.41354993G>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1339C>G" "" "Germline" "" "" "0" "" "" "g.40849088G>C" "" "likely benign" "" "0000409108" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409109" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "51G" "Variant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409110" "1" "33" "19" "41353611" "41353611" "subst" "0" "00008" "CYP2A6_000101" "g.41353611C>T" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2721G>A" "" "Germline" "" "" "0" "" "" "g.40847706C>T" "" "likely benign" "" "0000409111" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3225A>G" "" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409112" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "{PMID:Mwenifumbo 2008:18360915}" "" "2994T>C" "" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409113" "1" "33" "19" "41353017" "41353017" "subst" "0" "00008" "CYP2A6_000096" "g.41353017G>A" "" "{PMID:Mwenifumbo 2008:18360915}" "" "3315C>T" "" "Germline" "" "" "0" "" "" "g.40847112G>A" "" "likely benign" "" "0000409114" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "{PMID:Mwenifumbo 2008:18360915}" "" "4074delA" "" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409115" "1" "99" "19" "41349874" "41349874" "subst" "0" "00008" "CYP2A6_000032" "g.41349874T>A" "" "{PMID:Koudsi 2009:19365400}" "" "1312A>T" "" "Germline" "" "rs143731390" "0" "" "" "g.40843969T>A" "" "pathogenic" "" "0000409116" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "{PMID:Koudsi 2009:19365400}" "" "-1013A>G" "" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409117" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "{PMID:Koudsi 2009:19365400}" "" "-1289G>A" "" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409118" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "{PMID:Koudsi 2009:19365400}" "" "-1301A>C" "" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409119" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "{PMID:Koudsi 2009:19365400}" "" "3\' CYP2A7 conversion 6782C>G" "" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409120" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "{PMID:Koudsi 2009:19365400}" "" "gene conversion in the 3\' flanking region" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409121" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "{PMID:Koudsi 2009:19365400}" "" "3\' CYP2A7 conversion 7160A>G" "" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409122" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "{PMID:Koudsi 2009:19365400}" "" "6293T>C" "" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000409123" "1" "33" "19" "41350050" "41350050" "subst" "0" "00008" "CYP2A6_000039" "g.41350050T>C" "" "{PMID:Koudsi 2009:19365400}" "" "6282A>G" "" "Germline" "" "" "0" "" "" "g.40844145T>C" "" "likely benign" "" "0000409124" "1" "33" "19" "41350114" "41350114" "subst" "0" "00008" "CYP2A6_000040" "g.41350114T>C" "" "{PMID:Koudsi 2009:19365400}" "" "6218A>G" "" "Germline" "" "" "0" "" "" "g.40844209T>C" "" "likely benign" "" "0000409125" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Koudsi 2009:19365400}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409126" "1" "33" "19" "41355612" "41355612" "subst" "0" "00008" "CYP2A6_000137" "g.41355612C>T" "" "{PMID:Koudsi 2009:19365400}" "" "720G>A" "" "Germline" "" "" "0" "" "" "g.40849707C>T" "" "likely benign" "" "0000409127" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Koudsi 2009:19365400}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409128" "1" "33" "19" "41355195" "41355195" "subst" "0" "00008" "CYP2A6_000135" "g.41355195G>C" "" "{PMID:Koudsi 2009:19365400}" "" "1137C>G" "" "Germline" "" "" "0" "" "" "g.40849290G>C" "" "likely benign" "" "0000409129" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "{PMID:Koudsi 2009:19365400}" "" "2483G>A" "" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409130" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "{PMID:Koudsi 2009:19365400}" "" "3225A>G" "" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409131" "1" "33" "19" "41351309" "41351309" "subst" "8.13074E-5" "00008" "CYP2A6_000071" "g.41351309A>G" "" "{PMID:Bloom 2011:21597399}" "" "1051T>C" "" "Germline" "" "rs148166815" "0" "" "" "g.40845404A>G" "" "likely benign" "" "0000409132" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "{PMID:Piliguan 2014:24305170}" "" "1224C>T" "" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409133" "1" "33" "19" "41356161" "41356161" "subst" "0" "00008" "CYP2A6_000153" "g.41356161G>T" "" "{PMID:Piliguan 2014:24305170}" "" "171C>A" "" "Germline" "" "" "0" "" "" "g.40850256G>T" "" "likely benign" "" "0000409134" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Piliguan 2014:24305170}" "" "459G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409135" "1" "99" "19" "41355864" "41355864" "subst" "3.26086E-5" "00008" "CYP2A6_000145" "g.41355864C>T" "" "{PMID:Piliguan 2014:24305170}" "" "468G>A" "" "Germline" "" "rs143690364" "0" "" "" "g.40849959C>T" "" "pathogenic" "" "0000409136" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "{PMID:Piliguan 2014:24305170}" "" "1779G>A" "" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409137" "1" "99" "19" "41354565" "41354565" "subst" "0" "00008" "CYP2A6_000123" "g.41354565G>C" "" "{PMID:Piliguian 2014:24305170}" "" "447C>G" "" "Germline" "" "" "0" "" "" "g.40848660G>C" "" "pathogenic" "" "0000409138" "1" "33" "19" "41350602" "41350602" "subst" "0" "00008" "CYP2A6_000050" "g.41350602G>A" "" "{PMID:Piliguian 2014:24305170}" "" "1237C>T" "" "Germline" "" "" "0" "" "" "g.40844697G>A" "" "likely benign" "" "0000409139" "1" "33" "19" "41352840" "41352840" "subst" "0.0642769" "00008" "CYP2A6_000091" "g.41352840G>A" "" "{PMID:Piliguian 2014:24305170}" "" "771C>T" "" "Germline" "" "" "0" "" "" "g.40846935G>A" "" "likely benign" "" "0000409140" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "{PMID:Piliguian 2014:24305170}" "" "5738C>T" "" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409141" "1" "33" "19" "41356188" "41356188" "subst" "0.0690959" "00008" "CYP2A6_000154" "g.41356188C>T" "" "{PMID:Piliguian 2014:24305170}" "" "144G>A" "" "Germline" "" "" "0" "" "" "g.40850283C>T" "" "likely benign" "" "0000409142" "1" "33" "19" "41355825" "41355825" "subst" "0.0001222" "00008" "CYP2A6_000144" "g.41355825G>A" "" "{PMID:Piliguian 2014:24305170}" "" "241C>T" "" "Germline" "" "" "0" "" "" "g.40849920G>A" "" "likely benign" "" "0000409143" "1" "99" "19" "41352817" "41352817" "subst" "0.000174868" "00008" "CYP2A6_000090" "g.41352817C>T" "" "{PMID:Piliguian 2014:24305170}" "" "794G>A" "" "Germline" "" "rs140471703" "0" "" "" "g.40846912C>T" "" "pathogenic" "" "0000409144" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Piliguian 2014:24305170}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409145" "1" "99" "19" "41352808" "41352808" "subst" "4.06679E-5" "00008" "CYP2A6_000089" "g.41352808A>G" "" "{PMID:Piliguian 2014:24305170}" "" "803T>C" "" "Germline" "" "" "0" "" "" "g.40846903A>G" "" "pathogenic" "" "0000409146" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Piliguian 2014:24305170}" "" "1191T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409147" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Piliguian 2014:24305170}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409148" "1" "99" "19" "41351926" "41351926" "subst" "0" "00008" "CYP2A6_000080" "g.41351926G>A" "" "{PMID:Piliguian 2014:24305170}" "" "908C>T" "" "Germline" "" "" "0" "" "" "g.40846021G>A" "" "pathogenic" "" "0000409149" "1" "99" "19" "41350587" "41350587" "subst" "0.000953359" "00008" "CYP2A6_000047" "g.41350587T>C" "" "{PMID:Piliguian 2014:24305170}" "" "1252A>G" "" "Germline" "" "rs28399463" "0" "" "" "g.40844682T>C" "" "pathogenic" "" "0000409150" "1" "99" "19" "41350671" "41350671" "subst" "0.000122693" "00008" "CYP2A6_000057" "g.41350671C>T" "" "{PMID:Piliguian 2014:24305170}" "" "1168G>A" "" "Germline" "" "rs376817657" "0" "" "" "g.40844766C>T" "" "pathogenic" "" "0000409151" "1" "99" "19" "41350582" "41350582" "subst" "0.000810789" "00008" "CYP2A6_000046" "g.41350582C>G" "" "{PMID:Piliguian 2014:24305170}" "" "1257G>C" "" "Germline" "" "rs8192730" "0" "" "" "g.40844677C>G" "" "pathogenic" "" "0000409152" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "{PMID:Piliguian 2014:24305170}" "" "1245C>T" "" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409153" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "{PMID:Piliguian 2014:24305170}" "" "51G>A" "" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409154" "1" "33" "19" "41357493" "41357493" "subst" "0" "00008" "CYP2A6_000169" "g.41357493C>T" "" "{PMID:Haberl 2005:16041240}" "" "-1162G>A" "" "Germline" "" "" "0" "" "" "g.40851588C>T" "" "likely benign" "" "0000409155" "1" "33" "19" "41357900" "41357900" "subst" "0" "00008" "CYP2A6_000175" "g.41357900A>G" "" "{PMID:Haberl 2005:16041240}" "" "-1569T>C" "" "Germline" "" "" "0" "" "" "g.40851995A>G" "" "likely benign" "" "0000409156" "1" "33" "19" "41358221" "41358221" "subst" "0" "00008" "CYP2A6_000179" "g.41358221G>A" "" "{PMID:Haberl 2005:16041240}" "" "-1890C>T" "" "Germline" "" "" "0" "" "" "g.40852316G>A" "" "likely benign" "" "0000409157" "1" "33" "19" "41357975" "41357975" "subst" "0" "00008" "CYP2A6_000177" "g.41357975G>A" "" "{PMID:Haberl 2005:16041240}" "" "-1643C>T" "" "Germline" "" "" "0" "" "" "g.40852070G>A" "" "likely benign" "" "0000409158" "1" "33" "19" "41352762" "41352762" "subst" "0.0731151" "00008" "CYP2A6_000088" "g.41352762G>C" "" "{PMID:Haberl 2005:16041240}" "" "3570C>G" "" "Germline" "" "" "0" "" "" "g.40846857G>C" "" "likely benign" "" "0000409159" "1" "33" "19" "41351400" "41351400" "subst" "0.0454253" "00008" "CYP2A6_000073" "g.41351400G>A" "" "{PMID:Haberl 2005:16041240}" "" "4932C>T" "" "Germline" "" "" "0" "" "" "g.40845495G>A" "" "likely benign" "" "0000409160" "1" "33" "19" "41350509" "41350509" "subst" "0.0505333" "00008" "CYP2A6_000045" "g.41350509G>A" "" "{PMID:Haberl 2005:16041240}" "" "5823C>T" "" "Germline" "" "" "0" "" "" "g.40844604G>A" "" "likely benign" "" "0000409161" "1" "33" "19" "41350489" "41350489" "subst" "0.0674066" "00008" "CYP2A6_000043" "g.41350489C>G" "" "{PMID:Haberl 2005:16041240}" "" "5843G>C" "" "Germline" "" "" "0" "" "" "g.40844584C>G" "" "likely benign" "" "0000409162" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "{PMID:Haberl 2005:16041240}" "" "-745A>G" "" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409163" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Haberl 2005:16041240}" "" "5684T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409164" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "{PMID:Haberl 2005:16041240}" "" "5738C>T" "" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409165" "1" "33" "19" "41356188" "41356188" "subst" "0.0690959" "00008" "CYP2A6_000154" "g.41356188C>T" "" "{PMID:Haberl 2005:16041240}" "" "144G>A" "" "Germline" "" "" "0" "" "" "g.40850283C>T" "" "likely benign" "" "0000409166" "1" "33" "19" "41352840" "41352840" "subst" "0.0642769" "00008" "CYP2A6_000091" "g.41352840G>A" "" "{PMID:Haberl 2005:16041240}" "" "3492C>T" "" "Germline" "" "" "0" "" "" "g.40846935G>A" "" "likely benign" "" "0000409167" "1" "33" "19" "41354458" "41354458" "subst" "0" "00008" "CYP2A6_000117" "g.41354458C>A" "" "{PMID:Kiyotani 2002:15618701}" "" "1874G>T" "" "Germline" "" "" "0" "" "" "g.40848553C>A" "" "likely benign" "" "0000409168" "1" "33" "19" "41354442" "41354442" "subst" "0" "00008" "CYP2A6_000116" "g.41354442C>G" "" "{PMID:Kiyotani 2002:15618701}" "" "1890G>C" "" "Germline" "" "" "0" "" "" "g.40848537C>G" "" "likely benign" "" "0000409169" "1" "33" "19" "41354306" "41354306" "subst" "0.0184512" "00008" "CYP2A6_000115" "g.41354306G>A" "" "{PMID:Kiyotani 2002:15618701}" "" "2026C>T" "" "Germline" "" "" "0" "" "" "g.40848401G>A" "" "likely benign" "" "0000409170" "1" "33" "19" "41352762" "41352762" "subst" "0.0731151" "00008" "CYP2A6_000088" "g.41352762G>C" "" "{PMID:Kiyotani 2002:15618701}" "" "3570C>G" "" "Germline" "" "" "0" "" "" "g.40846857G>C" "" "likely benign" "" "0000409171" "1" "33" "19" "41351400" "41351400" "subst" "0" "00008" "CYP2A6_000074" "g.41351400G>T" "" "{PMID:Kiyotani 2002:15618701}" "" "4932C>A" "" "Germline" "" "" "0" "" "" "g.40845495G>T" "" "likely benign" "" "0000409172" "1" "33" "19" "41350996" "41350996" "subst" "0" "00008" "CYP2A6_000066" "g.41350996C>T" "" "{PMID:Kiyotani 2002:15618701}" "" "5336G>A" "" "Germline" "" "" "0" "" "" "g.40845091C>T" "" "likely benign" "" "0000409173" "1" "33" "19" "41349500" "41349500" "subst" "0" "00008" "CYP2A6_000018" "g.41349500T>C" "" "{PMID:Kiyotani 2002:15618701}" "" "6832A>G" "" "Germline" "" "" "0" "" "" "g.40843595T>C" "" "likely benign" "" "0000409174" "1" "33" "19" "41349497" "41349497" "subst" "0" "00008" "CYP2A6_000017" "g.41349497G>T" "" "{PMID:Kiyotani 2002:15618701}" "" "6835C>A" "" "Germline" "" "" "0" "" "" "g.40843592G>T" "" "likely benign" "" "0000409175" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "{PMID:Kiyotani 2002:15618701}" "" "6692C>G" "" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409176" "1" "33" "19" "41350050" "41350050" "subst" "0" "00008" "CYP2A6_000039" "g.41350050T>C" "" "{PMID:Kiyotani 2002:15618701}" "" "6282A>G" "" "Germline" "" "" "0" "" "" "g.40844145T>C" "" "likely benign" "" "0000409177" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "{PMID:Kiyotani 2002:15618701}" "" "6354T>C" "" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409178" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "{PMID:Kiyotani 2002:15618701}" "" "1620T>C" "" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409179" "1" "33" "19" "41354496" "41354496" "subst" "0.0793229" "00008" "CYP2A6_000118" "g.41354496C>A" "" "{PMID:Kiyotani 2002:15618701}" "" "1836G>T" "" "Germline" "" "" "0" "" "" "g.40848591C>A" "" "likely benign" "" "0000409180" "1" "33" "19" "41352936" "41352936" "subst" "0.0187923" "00008" "CYP2A6_000092" "g.41352936C>T" "" "{PMID:Kiyotani 2002:15618701}" "" "3396G>A" "" "Germline" "" "" "0" "" "" "g.40847031C>T" "" "likely benign" "" "0000409181" "1" "33" "19" "41351843" "41351843" "subst" "0.0299024" "00008" "CYP2A6_000079" "g.41351843G>A" "" "{PMID:Kiyotani 2002:15618701}" "" "4489C>T" "" "Germline" "" "" "0" "" "" "g.40845938G>A" "" "likely benign" "" "0000409182" "1" "33" "19" "41356123" "41356123" "subst" "0.0114568" "00008" "CYP2A6_000152" "g.41356123G>A" "" "{PMID:Saito 2003:12721789}" "" "209C>T" "" "Germline" "" "" "0" "" "" "g.40850218G>A" "" "likely benign" "" "0000409183" "1" "33" "19" "41355944" "41355944" "subst" "0" "00008" "CYP2A6_000149" "g.41355944G>C" "" "{PMID:Solus 2004:15469410}" "" "388C>G" "" "Germline" "" "" "0" "" "" "g.40850039G>C" "" "likely benign" "" "0000409184" "1" "33" "19" "41355718" "41355718" "del" "0" "00008" "CYP2A6_000139" "g.41355718del" "" "{PMID:Solus 2004:15469410}" "" "618delG" "" "Germline" "" "" "0" "" "" "g.40849813del" "" "likely benign" "" "0000409185" "1" "33" "19" "41353000" "41353000" "subst" "0.00145189" "00008" "CYP2A6_000095" "g.41353000C>T" "" "{PMID:Solus 2004:15469410}" "" "3332G>A" "" "Germline" "" "" "0" "" "" "g.40847095C>T" "" "likely benign" "" "0000409186" "1" "33" "19" "41351982" "41351982" "subst" "0.000862518" "00008" "CYP2A6_000081" "g.41351982C>T" "" "{PMID:Solus 2004:15469410}" "" "4350G>A" "" "Germline" "" "" "0" "" "" "g.40846077C>T" "" "likely benign" "" "0000409187" "1" "33" "19" "41351190" "41351190" "subst" "0.000223645" "00008" "CYP2A6_000069" "g.41351190G>A" "" "{PMID:Solus 2004:15469410}" "" "5142C>T" "" "Germline" "" "" "0" "" "" "g.40845285G>A" "" "likely benign" "" "0000409188" "1" "33" "19" "41350895" "41350895" "subst" "0" "00008" "CYP2A6_000065" "g.41350895G>A" "" "{PMID:Solus 2004:15469410}" "" "5437C>T" "" "Germline" "" "" "0" "" "" "g.40844990G>A" "" "likely benign" "" "0000409189" "1" "33" "19" "41350811" "41350811" "subst" "0" "00008" "CYP2A6_000064" "g.41350811T>A" "" "{PMID:Solus 2004:15469410}" "" "5521A>T" "" "Germline" "" "" "0" "" "" "g.40844906T>A" "" "likely benign" "" "0000409190" "1" "33" "19" "41350807" "41350807" "subst" "0" "00008" "CYP2A6_000063" "g.41350807C>G" "" "{PMID:Solus 2004:15469410}" "" "5525G>C" "" "Germline" "" "" "0" "" "" "g.40844902C>G" "" "likely benign" "" "0000409191" "1" "33" "19" "41350759" "41350759" "subst" "0" "00008" "CYP2A6_000061" "g.41350759T>G" "" "{PMID:Solus 2004:15469410}" "" "5573A>C" "" "Germline" "" "" "0" "" "" "g.40844854T>G" "" "likely benign" "" "0000409192" "1" "33" "19" "41349651" "41349651" "subst" "0" "00008" "CYP2A6_000026" "g.41349651T>C" "" "{PMID:Solus 2004:15469410}" "" "6681A>G" "" "Germline" "" "" "0" "" "" "g.40843746T>C" "" "likely benign" "" "0000409193" "1" "33" "19" "41349647" "41349647" "subst" "0" "00008" "CYP2A6_000025" "g.41349647G>A" "" "{PMID:Solus 2004:15469410}" "" "6685C>T" "" "Germline" "" "" "0" "" "" "g.40843742G>A" "" "likely benign" "" "0000409194" "1" "33" "19" "41349644" "41349644" "subst" "0" "00008" "CYP2A6_000024" "g.41349644T>C" "" "{PMID:Solus 2004:15469410}" "" "6688A>G" "" "Germline" "" "" "0" "" "" "g.40843739T>C" "" "likely benign" "" "0000409195" "1" "33" "19" "41349642" "41349642" "subst" "0" "00008" "CYP2A6_000023" "g.41349642T>C" "" "{PMID:Solus 2004:15469410}" "" "6690A>G" "" "Germline" "" "" "0" "" "" "g.40843737T>C" "" "likely benign" "" "0000409196" "1" "33" "19" "41349636" "41349636" "subst" "0" "00008" "CYP2A6_000020" "g.41349636G>A" "" "{PMID:Solus 2004:15469410}" "" "6696C>T" "" "Germline" "" "" "0" "" "" "g.40843731G>A" "" "likely benign" "" "0000409197" "1" "33" "19" "41356095" "41356095" "subst" "0" "00008" "CYP2A6_000151" "g.41356095C>T" "" "{PMID:Solus 2004:15469410}" "" "237G>A" "" "Germline" "" "" "0" "" "" "g.40850190C>T" "" "likely benign" "" "0000409198" "1" "33" "19" "41355919" "41355919" "subst" "0.0112313" "00008" "CYP2A6_000148" "g.41355919A>C" "" "{PMID:Solus 2004:15469410}" "" "413T>G" "" "Germline" "" "" "0" "" "" "g.40850014A>C" "" "likely benign" "" "0000409199" "1" "33" "19" "41350787" "41350787" "subst" "0" "00008" "CYP2A6_000062" "g.41350787C>G" "" "{PMID:Solus 2004:15469410}" "" "5545G>C" "" "Germline" "" "" "0" "" "" "g.40844882C>G" "" "likely benign" "" "0000409200" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "{PMID:Solus 2004:15469410}" "" "5684T>C" "" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409201" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "{PMID:Solus 2004:15469410}" "" "5717C>T" "" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409202" "1" "33" "19" "41349943" "41349943" "subst" "0" "00008" "CYP2A6_000034" "g.41349943G>C" "" "{PMID:Solus 2004:15469410}" "" "6389C>G" "" "Germline" "" "" "0" "" "" "g.40844038G>C" "" "likely benign" "" "0000409203" "1" "33" "19" "41349971" "41349971" "subst" "0" "00008" "CYP2A6_000036" "g.41349971G>T" "" "{PMID:Solus 2004:15469410}" "" "6361C>A" "" "Germline" "" "" "0" "" "" "g.40844066G>T" "" "likely benign" "" "0000409204" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "{PMID:Solus 2004:15469410}" "" "4636A>C" "" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409205" "1" "33" "19" "41355765" "41355765" "subst" "9.38469E-5" "00008" "CYP2A6_000142" "g.41355765G>A" "" "{PMID:Haberl 2005:16041240}" "" "567C>T" "" "Germline" "" "" "0" "" "" "g.40849860G>A" "" "likely benign" "" "0000409206" "1" "33" "19" "41354271" "41354271" "subst" "8.95168E-5" "00008" "CYP2A6_000112" "g.41354271A>C" "" "{PMID:Haberl 2005:16041240}" "" "2061T>G" "" "Germline" "" "" "0" "" "" "g.40848366A>C" "" "likely benign" "" "0000409207" "1" "33" "19" "41352817" "41352817" "subst" "0.000174868" "00008" "CYP2A6_000090" "g.41352817C>T" "" "{PMID:Haberl 2005:16041240}" "" "3515G>A" "" "Germline" "" "rs140471703" "0" "" "" "g.40846912C>T" "" "likely benign" "" "0000409208" "1" "33" "19" "41350671" "41350671" "subst" "0.000122693" "00008" "CYP2A6_000057" "g.41350671C>T" "" "{PMID:Haberl 2005:16041240}" "" "5661G>A" "" "Germline" "" "rs376817657" "0" "" "" "g.40844766C>T" "" "likely benign" "" "0000409209" "1" "33" "19" "41357457" "41357457" "subst" "0" "00008" "CYP2A6_000168" "g.41357457G>T" "" "{PMID:Haberl 2005:16041240}" "" "-1126C>A" "" "Germline" "" "" "0" "" "" "g.40851552G>T" "" "likely benign" "" "0000409210" "1" "33" "19" "41355775" "41355775" "subst" "0.00215231" "00008" "CYP2A6_000143" "g.41355775C>T" "" "{PMID:Haberl 2005:16041240}" "" "557G>A" "" "Germline" "" "" "0" "" "" "g.40849870C>T" "" "likely benign" "" "0000409211" "1" "33" "19" "41354297" "41354297" "subst" "3.26904E-5" "00008" "CYP2A6_000114" "g.41354297C>A" "" "{PMID:Haberl 2005:16041240}" "" "2035G>T" "" "Germline" "" "" "0" "" "" "g.40848392C>A" "" "likely benign" "" "0000409212" "1" "33" "19" "41354293" "41354293" "subst" "0" "00008" "CYP2A6_000113" "g.41354293A>G" "" "{PMID:Haberl 2005:16041240}" "" "2039T>C" "" "Germline" "" "" "0" "" "" "g.40848388A>G" "" "likely benign" "" "0000409213" "1" "33" "19" "41354174" "41354174" "subst" "0" "00008" "CYP2A6_000109" "g.41354174A>G" "" "{PMID:Haberl 2005:16041240}" "" "2158T>C" "" "Germline" "" "" "0" "" "" "g.40848269A>G" "" "likely benign" "" "0000409214" "1" "33" "19" "41354058" "41354058" "subst" "0" "00008" "CYP2A6_000105" "g.41354058C>G" "" "{PMID:Haberl 2005:16041240}" "" "2274G>C" "" "Germline" "" "" "0" "" "" "g.40848153C>G" "" "likely benign" "" "0000409215" "1" "33" "19" "41352139" "41352139" "subst" "0" "00008" "CYP2A6_000082" "g.41352139C>G" "" "{PMID:Haberl 2005:16041240}" "" "4193G>C" "" "Germline" "" "" "0" "" "" "g.40846234C>G" "" "likely benign" "" "0000409216" "1" "33" "19" "41351771" "41351771" "subst" "0" "00008" "CYP2A6_000078" "g.41351771C>T" "" "{PMID:Haberl 2005:16041240}" "" "4561G>A" "" "Germline" "" "" "0" "" "" "g.40845866C>T" "" "likely benign" "" "0000409217" "1" "33" "19" "41351170" "41351170" "subst" "0.00313616" "00008" "CYP2A6_000068" "g.41351170G>A" "" "{PMID:Haberl 2005:16041240}" "" "5162C>T" "" "Germline" "" "" "0" "" "" "g.40845265G>A" "" "likely benign" "" "0000409218" "1" "33" "19" "41350696" "41350696" "subst" "0.000753497" "00008" "CYP2A6_000059" "g.41350696T>G" "" "{PMID:Haberl 2005:16041240}" "" "5636A>C" "" "Germline" "" "" "0" "" "" "g.40844791T>G" "" "likely benign" "" "0000409219" "1" "33" "19" "41350672" "41350672" "subst" "0.000806366" "00008" "CYP2A6_000058" "g.41350672G>A" "" "{PMID:Haberl 2005:16041240}" "" "5660C>T" "" "Germline" "" "" "0" "" "" "g.40844767G>A" "" "likely benign" "" "0000409220" "1" "33" "19" "41350600" "41350600" "subst" "0.00159792" "00008" "CYP2A6_000049" "g.41350600G>A" "" "{PMID:Haberl 2005:16041240}" "" "5732C>T" "" "Germline" "" "" "0" "" "" "g.40844695G>A" "" "likely benign" "" "0000409221" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "{PMID:Haberl 2005:16041240}" "" "6586T>C" "" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409222" "1" "33" "19" "41355865" "41355865" "subst" "0.00100678" "00008" "CYP2A6_000146" "g.41355865G>A" "" "{PMID:Haberl 2005:16041240}" "" "467C>T" "" "Germline" "" "" "0" "" "" "g.40849960G>A" "" "likely benign" "" "0000409223" "1" "33" "19" "41355754" "41355754" "subst" "0.00106515" "00008" "CYP2A6_000141" "g.41355754T>C" "" "{PMID:Haberl 2005:16041240}" "" "578A>G" "" "Germline" "" "" "0" "" "" "g.40849849T>C" "" "likely benign" "" "0000409224" "1" "33" "19" "41354622" "41354622" "subst" "0.000256983" "00008" "CYP2A6_000125" "g.41354622G>A" "" "{PMID:Haberl 2005:16041240}" "" "1710C>T" "" "Germline" "" "" "0" "" "" "g.40848717G>A" "" "likely benign" "" "0000409225" "1" "33" "19" "41353017" "41353017" "subst" "0" "00008" "CYP2A6_000096" "g.41353017G>A" "" "{PMID:Haberl 2005:16041240}" "" "3315C>T" "" "Germline" "" "" "0" "" "" "g.40847112G>A" "" "likely benign" "" "0000409226" "1" "99" "19" "41349626" "4294967295" "" "0" "00008" "CYP2A6_000006" "g.(41349626_?)con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B" "Germline" "" "" "0" "" "" "" "" "pathogenic" "" "0000409227" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B2" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409228" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B2" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409229" "1" "33" "19" "41356727" "41356727" "subst" "0" "00008" "CYP2A6_000162" "g.41356727C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-395G>A" "reference haplotype CYP2A6*1C" "Germline" "" "" "0" "" "" "g.40850822C>T" "" "likely benign" "" "0000409230" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1C" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409231" "1" "33" "19" "41349250" "41349259" "" "0" "00008" "CYP2A6_000007" "g.41349250_41349259con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion at 7073-7082" "reference haplotype CYP2A6*1B4" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409232" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B4" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409233" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409234" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409235" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409236" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409237" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409238" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409239" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B5" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409240" "1" "33" "19" "41355068" "41355068" "subst" "0" "00008" "CYP2A6_000133" "g.41355068G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6285A>G" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40849163G>C" "" "likely benign" "" "0000409241" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409242" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409243" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409244" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409245" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409246" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409247" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6293T>C" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000409248" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B6" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409249" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409250" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409251" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1464A>T" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000409252" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409253" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409254" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409255" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B7" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409256" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409257" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409258" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409259" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1464A>T" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000409260" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409261" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409262" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409263" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B8" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409264" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409265" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409266" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409267" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1464A>T" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000409268" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409269" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409270" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409271" "1" "33" "19" "41349943" "41349943" "subst" "0" "00008" "CYP2A6_000034" "g.41349943G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6389C>G" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40844038G>C" "" "likely benign" "" "0000409272" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B10" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409273" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409274" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409275" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409276" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1464A>T" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000409277" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409278" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409279" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409280" "1" "33" "19" "41350704" "41350704" "subst" "0.000777281" "00008" "CYP2A6_000060" "g.41350704G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5628C>T" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40844799G>A" "" "likely benign" "" "0000409281" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B11" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409282" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B12" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409283" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*1B12" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409284" "1" "33" "19" "41349641" "41349641" "subst" "0" "00008" "CYP2A6_000022" "g.41349641G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1545C>G" "reference haplotype CYP2A6*1B13" "Germline" "" "" "0" "" "" "g.40843736G>C" "" "likely benign" "" "0000409285" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*1B13" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409286" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B13" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409287" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "22C>T" "reference haplotype CYP2A6*1B13" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409288" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1636C>G" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409289" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000409290" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409291" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7160A>G" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409292" "1" "33" "19" "41355994" "41355994" "subst" "0" "00008" "CYP2A6_000150" "g.41355994A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "338T>C" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "g.40850089A>G" "" "likely benign" "" "0000409293" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*1B14" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409294" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1636C>G" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409295" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1191T>C" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409296" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409297" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409298" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409299" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000409300" "1" "33" "19" "41349372" "41349373" "ins" "0" "00008" "CYP2A6_000014" "g.41349372_41349373insTTTTCC" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6960_6961insGAAAAG" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843467_40843468insTTTTCC" "" "likely benign" "" "0000409301" "1" "33" "19" "41349343" "41349343" "subst" "0" "00008" "CYP2A6_000013" "g.41349343T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6989A>G" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843438T>C" "" "likely benign" "" "0000409302" "1" "33" "19" "41349323" "41349324" "delins" "0" "00008" "CYP2A6_000012" "g.41349323_41349324delinsTAGAGC" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7008_7009TC>GCTCTA" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843418_40843419delinsTAGAGC" "" "likely benign" "" "0000409304" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7160A>G" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409305" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "22C>T" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409306" "1" "33" "19" "41354702" "41354702" "subst" "0.00300286" "00008" "CYP2A6_000130" "g.41354702A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1630T>C" "reference haplotype CYP2A6*1B16" "Germline" "" "" "0" "" "" "g.40848797A>G" "" "likely benign" "" "0000409307" "1" "33" "19" "41351355" "41351355" "subst" "6.0987E-5" "00008" "CYP2A6_000072" "g.41351355G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1005C>T" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40845450G>A" "" "likely benign" "" "0000409308" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6782C>G" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409309" "1" "33" "19" "41349500" "41349500" "subst" "0" "00008" "CYP2A6_000018" "g.41349500T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6832A>G" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843595T>C" "" "likely benign" "" "0000409310" "1" "33" "19" "41349497" "41349497" "subst" "0" "00008" "CYP2A6_000017" "g.41349497G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6835C>A" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843592G>T" "" "likely benign" "" "0000409311" "1" "33" "19" "41349397" "41349398" "ins" "0" "00008" "CYP2A6_000015" "g.41349397_41349398insAGTGA" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6935_6936insCACTT" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843492_40843493insAGTGA" "" "likely benign" "" "0000409312" "1" "33" "19" "41349372" "41349373" "ins" "0" "00008" "CYP2A6_000014" "g.41349372_41349373insTTTTCC" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6960_6961insGAAAAG" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843467_40843468insTTTTCC" "" "likely benign" "" "0000409313" "1" "33" "19" "41349343" "41349343" "subst" "0" "00008" "CYP2A6_000013" "g.41349343T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6989A>G" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843438T>C" "" "likely benign" "" "0000409315" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7160A>G" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409316" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*1B17\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409317" "1" "33" "19" "41350189" "41350189" "subst" "0" "00008" "CYP2A6_000041" "g.41350189G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6143C>A" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40844284G>T" "" "likely benign" "" "0000409318" "1" "33" "19" "41354686" "41354686" "subst" "0" "00008" "CYP2A6_000129" "g.41354686G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1646C>T" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40848781G>A" "" "likely benign" "" "0000409319" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409320" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409321" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409322" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2296C>T" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409323" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409324" "1" "33" "19" "41352544" "41352544" "subst" "0" "00008" "CYP2A6_000087" "g.41352544G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3788C>T" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40846639G>A" "" "likely benign" "" "0000409325" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4071delA" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409326" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4636A>C" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409327" "1" "33" "19" "41351482" "41351482" "subst" "0" "00008" "CYP2A6_000075" "g.41351482G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4850C>T" "reference haplotype CYP2A6*1B17" "Germline" "" "" "0" "" "" "g.40845577G>A" "" "likely benign" "" "0000409328" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1D" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409329" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1224C>T" "reference haplotype CYP2A6*1F" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409330" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1224C>T" "reference haplotype CYP2A6*1G" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409331" "1" "33" "19" "41350507" "41350507" "subst" "0.0110735" "00008" "CYP2A6_000044" "g.41350507T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5825A>G" "reference haplotype CYP2A6*1G" "Germline" "" "" "0" "" "" "g.40844602T>C" "" "likely benign" "" "0000409332" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*1H" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409333" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*1J" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409334" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*1J" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409335" "1" "33" "19" "41357530" "41357531" "ins" "0" "00008" "CYP2A6_000170" "g.41357530_41357531insN[316]" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1199_-1198ins316bpAlu" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409336" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409337" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409338" "1" "33" "19" "41357018" "41357018" "subst" "0" "00008" "CYP2A6_000164" "g.41357018T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-686A>G" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40851113T>C" "" "likely benign" "" "0000409339" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7160A>G" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409340" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*1K\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409341" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409342" "1" "33" "19" "41355901" "41355901" "subst" "0.00014733" "00008" "CYP2A6_000147" "g.41355901G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "431C>T" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40849996G>A" "" "likely benign" "" "0000409343" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "459G>A" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409344" "1" "33" "19" "41352954" "41352954" "subst" "0" "00008" "CYP2A6_000094" "g.41352954G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "657C>T" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40847049G>A" "" "likely benign" "" "0000409345" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409346" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1779G>A" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409347" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*1K\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409348" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409349" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409350" "1" "33" "19" "41352954" "41352954" "subst" "0" "00008" "CYP2A6_000094" "g.41352954G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3378C>T" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40847049G>A" "" "likely benign" "" "0000409351" "1" "33" "19" "41352428" "41352428" "subst" "0" "00008" "CYP2A6_000085" "g.41352428C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3904G>A" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40846523C>T" "" "likely benign" "" "0000409352" "1" "33" "19" "41352268" "41352268" "del" "0" "00008" "CYP2A6_000084" "g.41352268del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4074delA" "reference haplotype CYP2A6*1K" "Germline" "" "" "0" "" "" "g.40846363del" "" "likely benign" "" "0000409353" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion at 7073-7082" "reference haplotype CYP2A6*1L" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409354" "1" "33" "19" "41349443" "41356352" "dup" "0" "00008" "CYP2A6_000016" "g.(?_41349443)_(41356352_?)dup" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "c.(?_-21)_(*258_?)dup" "reference haplotype CYP2A6*1X2A" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409355" "1" "33" "19" "41349443" "41356352" "dup" "0" "00008" "CYP2A6_000016" "g.(?_41349443)_(41356352_?)dup" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "c.(?_-21)_(*258_?)dup" "reference haplotype CYP2A6*1X2B" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409356" "1" "99" "19" "41354533" "41354533" "subst" "0.0197392" "00008" "CYP2A6_000119" "g.41354533A>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "479T>A" "reference haplotype CYP2A6*2" "Germline" "" "rs1801272" "0" "" "" "g.40848628A>T" "" "pathogenic" "" "0000409357" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*2" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409358" "1" "99" "19" "41349750" "41349750" "subst" "0" "00008" "CYP2A6_000029" "g.41349750C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1436G>T" "reference haplotype CYP2A6*5" "Germline" "" "rs5031017" "0" "" "" "g.40843845C>A" "" "pathogenic" "" "0000409359" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*5" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409360" "1" "33" "19" "41354629" "41354629" "subst" "2.85717E-5" "00008" "CYP2A6_000126" "g.41354629C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "383G>A" "reference haplotype CYP2A6*6" "Germline" "" "" "0" "" "" "g.40848724C>T" "" "likely benign" "" "0000409361" "1" "99" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1412T>C" "reference haplotype CYP2A6*7" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "pathogenic" "" "0000409362" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*7" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409363" "1" "11" "19" "41349732" "41349732" "subst" "0.00164576" "00008" "CYP2A6_000027" "g.41349732C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1454G>T" "reference haplotype CYP2A6*8" "Germline" "" "rs28399468" "0" "" "" "g.40843827C>A" "" "benign" "" "0000409364" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*8" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409365" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*9A" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409366" "1" "99" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-48T>G" "reference haplotype CYP2A6*9A" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "pathogenic" "" "0000409367" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1547C>G" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409368" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409369" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409370" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409371" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409372" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-48T>G" "reference haplotype CYP2A6*9B" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000409373" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409374" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409375" "1" "33" "19" "41354496" "41354496" "subst" "0.0793229" "00008" "CYP2A6_000118" "g.41354496C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1836G>T" "reference haplotype CYP2A6*9B" "Germline" "" "" "0" "" "" "g.40848591C>A" "" "likely benign" "" "0000409376" "1" "99" "19" "41349732" "41349732" "subst" "0.00164576" "00008" "CYP2A6_000027" "g.41349732C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1454G>T" "reference haplotype CYP2A6*10" "Germline" "" "rs28399468" "0" "" "" "g.40843827C>A" "" "pathogenic" "" "0000409377" "1" "99" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1412T>C" "reference haplotype CYP2A6*10" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "pathogenic" "" "0000409378" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*10" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409379" "1" "99" "19" "41352941" "41352941" "subst" "0.00103497" "00008" "CYP2A6_000093" "g.41352941A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "670T>C" "reference haplotype CYP2A6*11" "Germline" "" "rs28399447" "0" "" "" "g.40847036A>G" "" "pathogenic" "" "0000409380" "1" "99" "19" "41349443" "41354669" "" "0" "00008" "CYP2A6_000009" "g.(?_41349443)_(41354669_41355722)con(?_41388657)_(41386150_41386383)" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "exons1-2ofCYP2A7origin" "reference haplotype CYP2A6*12A" "Germline" "" "" "0" "" "" "" "" "pathogenic" "" "0000409381" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1547C>G" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409382" "1" "33" "19" "41351169" "41351169" "subst" "0.0301293" "00008" "CYP2A6_000067" "g.41351169C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5163G>A" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40845264C>T" "" "likely benign" "" "0000409383" "1" "33" "19" "41350787" "41350787" "subst" "0" "00008" "CYP2A6_000062" "g.41350787C>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5545G>C" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40844882C>G" "" "likely benign" "" "0000409384" "1" "33" "19" "41350615" "41350615" "subst" "0" "00008" "CYP2A6_000052" "g.41350615G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5717C>G" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40844710G>C" "" "likely benign" "" "0000409385" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409386" "1" "33" "19" "41352936" "41352936" "subst" "0.0187923" "00008" "CYP2A6_000092" "g.41352936C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3396G>A" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40847031C>T" "" "likely benign" "" "0000409387" "1" "33" "19" "41351843" "41351843" "subst" "0.0299024" "00008" "CYP2A6_000079" "g.41351843G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4489C>T" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "g.40845938G>A" "" "likely benign" "" "0000409388" "1" "33" "19" "41349443" "41354669" "" "0" "00008" "CYP2A6_000009" "g.(?_41349443)_(41354669_41355722)con(?_41388657)_(41386150_41386383)" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "exons1-2ofCYP2A7origin" "reference haplotype CYP2A6*12B" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409389" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-48T>G" "reference haplotype CYP2A6*13" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000409390" "1" "33" "19" "41356319" "41356319" "subst" "3.2719E-5" "00008" "CYP2A6_000160" "g.41356319C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "13G>A" "reference haplotype CYP2A6*13" "Germline" "" "rs28399434" "0" "" "" "g.40850414C>T" "" "likely benign" "" "0000409391" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*14" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409392" "1" "33" "19" "41356246" "41356246" "subst" "0.0286566" "00008" "CYP2A6_000155" "g.41356246C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "86G>A" "reference haplotype CYP2A6*14" "Germline" "" "rs28399435" "0" "" "" "g.40850341C>T" "" "likely benign" "" "0000409393" "1" "33" "19" "41354198" "41354198" "subst" "0.000577358" "00008" "CYP2A6_000111" "g.41354198T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "580A>G" "reference haplotype CYP2A6*15" "Germline" "" "" "0" "" "" "g.40848293T>C" "" "likely benign" "" "0000409394" "1" "33" "19" "41356379" "41356379" "subst" "0.103226" "00008" "CYP2A6_000161" "g.41356379A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-48T>G" "reference haplotype CYP2A6*15" "Germline" "" "rs28399433" "0" "" "" "g.40850474A>C" "" "likely benign" "" "0000409395" "1" "33" "19" "41354171" "41354171" "subst" "0.00010978" "00008" "CYP2A6_000107" "g.41354171G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "607C>A" "reference haplotype CYP2A6*16" "Germline" "" "rs56256500" "0" "" "" "g.40848266G>T" "" "likely benign" "" "0000409396" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1224C>T" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409397" "1" "99" "19" "41351267" "41351267" "subst" "0.00798878" "00008" "CYP2A6_000070" "g.41351267C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1093G>A" "reference haplotype CYP2A6*17" "Germline" "" "rs28399454" "0" "" "" "g.40845362C>T" "" "pathogenic" "" "0000409398" "1" "33" "19" "41351169" "41351169" "subst" "0.0301293" "00008" "CYP2A6_000067" "g.41351169C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5163G>A" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40845264C>T" "" "likely benign" "" "0000409399" "1" "33" "19" "41350507" "41350507" "subst" "0.0110735" "00008" "CYP2A6_000044" "g.41350507T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5825A>G" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40844602T>C" "" "likely benign" "" "0000409400" "1" "33" "19" "41356123" "41356123" "subst" "0.0114568" "00008" "CYP2A6_000152" "g.41356123G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "209C>T" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40850218G>A" "" "likely benign" "" "0000409401" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "459G>A" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409402" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1779G>A" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409403" "1" "33" "19" "41351843" "41351843" "subst" "0.0299024" "00008" "CYP2A6_000079" "g.41351843G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4489C>T" "reference haplotype CYP2A6*17" "Germline" "" "" "0" "" "" "g.40845938G>A" "" "likely benign" "" "0000409404" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1175A>T" "reference haplotype CYP2A6*18A\r\nVariant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000409405" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1175A>T" "reference haplotype CYP2A6*18B\r\nVariant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000409406" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1191T>C" "reference haplotype CYP2A6*18B" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409407" "1" "33" "19" "41350630" "41350630" "subst" "0.00513267" "00008" "CYP2A6_000053" "g.41350630A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1209T>C" "reference haplotype CYP2A6*18B" "Germline" "" "" "0" "" "" "g.40844725A>G" "" "likely benign" "" "0000409408" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*18B" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409409" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1175A>T" "reference haplotype CYP2A6*18C\r\nVariant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000409410" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1546C>G" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409411" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409412" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409413" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409414" "1" "33" "19" "41357795" "41357795" "subst" "0" "00008" "CYP2A6_000174" "g.41357795T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1464A>T" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40851890T>A" "" "likely benign" "" "0000409415" "1" "33" "19" "41357910" "41357910" "subst" "0" "00008" "CYP2A6_000176" "g.41357910A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1579T>C" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40852005A>G" "" "likely benign" "" "0000409416" "1" "33" "19" "41358011" "41358011" "subst" "0" "00008" "CYP2A6_000178" "g.41358011T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1680A>G" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40852106T>C" "" "likely benign" "" "0000409417" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*18C" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409418" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000056" "g.41350664T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1175A>T" "reference haplotype CYP2A6*19\r\nVariant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message." "Germline" "" "rs1809810" "0" "" "" "" "" "likely benign" "" "0000409419" "1" "33" "19" "41349774" "41349774" "subst" "0.00775191" "00008" "CYP2A6_000031" "g.41349774A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1412T>C" "reference haplotype CYP2A6*19" "Germline" "" "rs5031016" "0" "" "" "g.40843869A>G" "" "likely benign" "" "0000409420" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*19" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409421" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*19" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409422" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1191T>C" "reference haplotype CYP2A6*20" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409423" "1" "99" "19" "41354191" "41354192" "del" "0" "00008" "CYP2A6_000110" "g.41354191_41354192del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "587_588del" "reference haplotype CYP2A6*20" "Germline" "" "" "0" "" "" "g.40848286_40848287del" "" "pathogenic" "" "0000409424" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1546C>G" "reference haplotype CYP2A6*20" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409425" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*20" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409426" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2296C>T" "reference haplotype CYP2A6*20" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409427" "1" "99" "19" "41349759" "41349759" "subst" "0.0123454" "00008" "CYP2A6_000030" "g.41349759T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1427A>G" "reference haplotype CYP2A6*21" "Germline" "" "rs6413474" "0" "" "" "g.40843854T>C" "" "pathogenic" "" "0000409428" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*21" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409429" "1" "33" "19" "41354538" "41354538" "subst" "0.000655264" "00008" "CYP2A6_000121" "g.41354538G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "474C>G" "reference haplotype CYP2A6*22" "Germline" "" "rs60605885" "0" "" "" "g.40848633G>C" "" "likely benign" "" "0000409430" "1" "33" "19" "41354534" "41354534" "subst" "0" "00008" "CYP2A6_000120" "g.41354534G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "478C>A" "reference haplotype CYP2A6*22" "Germline" "" "rs60563539" "0" "" "" "g.40848629G>T" "" "likely benign" "" "0000409431" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*22" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409432" "1" "99" "19" "41354171" "41354171" "subst" "0.00106121" "00008" "CYP2A6_000108" "g.41354171G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "607C>T" "reference haplotype CYP2A6*23" "Germline" "" "" "0" "" "" "g.40848266G>A" "" "pathogenic" "" "0000409433" "1" "99" "19" "41349874" "41349874" "subst" "0" "00008" "CYP2A6_000032" "g.41349874T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1312A>T" "reference haplotype CYP2A6*24A" "Germline" "" "rs143731390" "0" "" "" "g.40843969T>A" "" "pathogenic" "" "0000409434" "1" "99" "19" "41355738" "41355738" "subst" "0.000735986" "00008" "CYP2A6_000140" "g.41355738C>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "328G>C" "reference haplotype CYP2A6*24A" "Germline" "" "rs72549435" "0" "" "" "g.40849833C>G" "" "pathogenic" "" "0000409435" "1" "33" "19" "41355754" "41355754" "subst" "0.00106515" "00008" "CYP2A6_000141" "g.41355754T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "312A>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40849849T>C" "" "likely benign" "" "0000409436" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409437" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409438" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409439" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6782C>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409440" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409441" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*24A\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409442" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6293T>C" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000409443" "1" "33" "19" "41350050" "41350050" "subst" "0" "00008" "CYP2A6_000039" "g.41350050T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6282A>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40844145T>C" "" "likely benign" "" "0000409444" "1" "33" "19" "41350114" "41350114" "subst" "0" "00008" "CYP2A6_000040" "g.41350114T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6218A>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40844209T>C" "" "likely benign" "" "0000409445" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409446" "1" "33" "19" "41355612" "41355612" "subst" "0" "00008" "CYP2A6_000137" "g.41355612C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "720G>A" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40849707C>T" "" "likely benign" "" "0000409447" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409448" "1" "33" "19" "41355195" "41355195" "subst" "0" "00008" "CYP2A6_000135" "g.41355195G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1137C>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40849290G>C" "" "likely benign" "" "0000409449" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*24A\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409450" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409451" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3225A>G" "reference haplotype CYP2A6*24A" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409452" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1440T>C" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409453" "1" "33" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "352T>C" "reference haplotype CYP2A6*25" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "likely benign" "" "0000409454" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409455" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409456" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409457" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7160A>G" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409458" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6692C>G" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409459" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*25\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409460" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "22C>T" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409461" "1" "33" "19" "41355564" "41355564" "subst" "0" "00008" "CYP2A6_000136" "g.41355564T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "768A>T" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40849659T>A" "" "likely benign" "" "0000409462" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409463" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*25\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409464" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409465" "1" "33" "19" "41353727" "41353727" "subst" "0" "00008" "CYP2A6_000102" "g.41353727C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2605G>A" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40847822C>T" "" "likely benign" "" "0000409466" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2296C>T" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409467" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409468" "1" "33" "19" "41353411" "41353411" "subst" "0" "00008" "CYP2A6_000100" "g.41353411C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2921G>A" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40847506C>T" "" "likely benign" "" "0000409469" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4636A>C" "reference haplotype CYP2A6*25" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409470" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1440T>C" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409471" "1" "99" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "352T>C" "reference haplotype CYP2A6*26" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "pathogenic" "" "0000409472" "1" "99" "19" "41354629" "41354629" "subst" "0.00026939" "00008" "CYP2A6_000127" "g.41354629C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "383G>T" "reference haplotype CYP2A6*26" "Germline" "" "rs4986891" "0" "" "" "g.40848724C>A" "" "pathogenic" "" "0000409473" "1" "33" "19" "41354622" "41354622" "subst" "0.000256983" "00008" "CYP2A6_000125" "g.41354622G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "390C>T" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40848717G>A" "" "likely benign" "" "0000409474" "1" "99" "19" "41354621" "41354621" "subst" "0.000256942" "00008" "CYP2A6_000124" "g.41354621A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "391T>G" "reference haplotype CYP2A6*26" "Germline" "" "rs59552350" "0" "" "" "g.40848716A>C" "" "pathogenic" "" "0000409475" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409476" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409477" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409478" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*26\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409479" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "22C>T" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409480" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409481" "1" "33" "19" "41355167" "41355167" "subst" "0" "00008" "CYP2A6_000134" "g.41355167C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1165G>A" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40849262C>T" "" "likely benign" "" "0000409482" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*26\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409483" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409484" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2296C>T" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409485" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409486" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4071delA" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409487" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4636A>C" "reference haplotype CYP2A6*26" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409488" "1" "33" "19" "41354169" "41354170" "delins" "0" "00008" "CYP2A6_000106" "g.41354169_41354170delinsT" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "608_609GC>A" "reference haplotype CYP2A6*27" "Germline" "" "rs28399445" "0" "" "" "g.40848264_40848265delinsT" "" "likely benign" "" "0000409489" "1" "33" "19" "41349746" "41349746" "subst" "0.000948705" "00008" "CYP2A6_000028" "g.41349746A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1440T>C" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40843841A>G" "" "likely benign" "" "0000409490" "1" "33" "19" "41354660" "41354660" "subst" "0.00093302" "00008" "CYP2A6_000128" "g.41354660A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "352T>C" "reference haplotype CYP2A6*27" "Germline" "" "rs2839940" "0" "" "" "g.40848755A>G" "" "likely benign" "" "0000409491" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409492" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409493" "1" "33" "19" "41357077" "41357077" "subst" "0" "00008" "CYP2A6_000165" "g.41357077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-745A>G" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40851172T>C" "" "likely benign" "" "0000409494" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7160A>G" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409495" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6692C>G" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409496" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*27\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409497" "1" "33" "19" "41350475" "41350475" "subst" "0" "00008" "CYP2A6_000042" "g.41350475A>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5857T>A" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40844570A>T" "" "likely benign" "" "0000409498" "1" "33" "19" "41356310" "41356310" "subst" "0.0221428" "00008" "CYP2A6_000158" "g.41356310G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "22C>T" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40850405G>A" "" "likely benign" "" "0000409499" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409500" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*27\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409501" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409502" "1" "33" "19" "41354036" "41354036" "subst" "0" "00008" "CYP2A6_000104" "g.41354036G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2296C>T" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40848131G>A" "" "likely benign" "" "0000409503" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409504" "1" "33" "19" "41352460" "41352460" "subst" "0" "00008" "CYP2A6_000086" "g.41352460C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3872G>A" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40846555C>T" "" "likely benign" "" "0000409505" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4071delA" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409506" "1" "33" "19" "41351696" "41351696" "subst" "0" "00008" "CYP2A6_000077" "g.41351696T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4636A>C" "reference haplotype CYP2A6*27" "Germline" "" "" "0" "" "" "g.40845791T>G" "" "likely benign" "" "0000409507" "1" "33" "19" "41350587" "41350587" "subst" "0.000953359" "00008" "CYP2A6_000047" "g.41350587T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1252A>G" "reference haplotype CYP2A6*28A" "Germline" "" "rs28399463" "0" "" "" "g.40844682T>C" "" "likely benign" "" "0000409508" "1" "33" "19" "41350582" "41350582" "subst" "0.000810789" "00008" "CYP2A6_000046" "g.41350582C>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1257G>C" "reference haplotype CYP2A6*28A" "Germline" "" "rs8192730" "0" "" "" "g.40844677C>G" "" "likely benign" "" "0000409509" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1245C>T" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409510" "1" "33" "19" "41357600" "41357600" "subst" "0" "00008" "CYP2A6_000171" "g.41357600A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1269T>C" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40851695A>G" "" "likely benign" "" "0000409511" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6782C>G" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409512" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409513" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7160A>G" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409514" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*28A\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409515" "1" "33" "19" "41349942" "41349942" "subst" "0" "00008" "CYP2A6_000033" "g.41349942A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6390T>C" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844037A>G" "" "likely benign" "" "0000409516" "1" "33" "19" "41349943" "41349943" "subst" "0" "00008" "CYP2A6_000034" "g.41349943G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6389C>G" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844038G>C" "" "likely benign" "" "0000409517" "1" "33" "19" "41349947" "41349947" "subst" "0" "00008" "CYP2A6_000035" "g.41349947C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6385G>T" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844042C>A" "" "likely benign" "" "0000409518" "1" "33" "19" "41349971" "41349971" "subst" "0" "00008" "CYP2A6_000036" "g.41349971G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6361C>A" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844066G>T" "" "likely benign" "" "0000409519" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409520" "1" "33" "19" "41355676" "41355676" "subst" "0.00172034" "00008" "CYP2A6_000138" "g.41355676C>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "656G>T" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40849771C>A" "" "likely benign" "" "0000409521" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409522" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409523" "1" "33" "19" "41351651" "41351651" "subst" "0" "00008" "CYP2A6_000076" "g.41351651A>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4681T>G" "reference haplotype CYP2A6*28A" "Germline" "" "" "0" "" "" "g.40845746A>C" "" "likely benign" "" "0000409524" "1" "33" "19" "41353077" "41353077" "subst" "0" "00008" "CYP2A6_000097" "g.41353077T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3255A>G" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40847172T>C" "" "likely benign" "" "0000409525" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409526" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409527" "1" "33" "19" "41356801" "41356823" "delins" "0" "00008" "CYP2A6_000163" "g.41356801_41356823delinsCAGATTCCACATATGGATT" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-492_-470delCCCCTTCCTGAGACCCTTAACCCinsAATCCATATGTGGAATCTG" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40850896_40850918delinsCAGATTCCACATATGGATT" "" "likely benign" "" "0000409528" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7160A>G" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409529" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6692C>G" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409530" "1" "33" "19" "41348764" "41348764" "subst" "0" "00008" "CYP2A6_000010" "g.41348764G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7568C>T" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40842859G>A" "" "likely benign" "" "0000409531" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*31A\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409532" "1" "33" "19" "41356316" "41356316" "subst" "0.00107459" "00008" "CYP2A6_000159" "g.41356316T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "16A>C" "reference haplotype CYP2A6*31A" "Germline" "" "rs72549432" "0" "" "" "g.40850411T>G" "" "likely benign" "" "0000409533" "1" "33" "19" "41354993" "41354993" "subst" "0" "00008" "CYP2A6_000132" "g.41354993G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1339C>G" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40849088G>C" "" "likely benign" "" "0000409534" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409535" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*31A\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409536" "1" "33" "19" "41353611" "41353611" "subst" "0" "00008" "CYP2A6_000101" "g.41353611C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2721G>A" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40847706C>T" "" "likely benign" "" "0000409537" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409538" "1" "33" "19" "41353017" "41353017" "subst" "0" "00008" "CYP2A6_000096" "g.41353017G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3315C>T" "reference haplotype CYP2A6*31A" "Germline" "" "" "0" "" "" "g.40847112G>A" "" "likely benign" "" "0000409539" "1" "33" "19" "41355865" "41355865" "subst" "0.00100678" "00008" "CYP2A6_000146" "g.41355865G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "201C>T" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40849960G>A" "" "likely benign" "" "0000409540" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409541" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409542" "1" "33" "19" "41356801" "41356823" "delins" "0" "00008" "CYP2A6_000163" "g.41356801_41356823delinsCAGATTCCACATATGGATT" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-492_-470delCCCCTTCCTGAGACCCTTAACCCinsAATCCATATGTGGAATCTG" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40850896_40850918delinsCAGATTCCACATATGGATT" "" "likely benign" "" "0000409543" "1" "33" "19" "41357306" "41357306" "subst" "0" "00008" "CYP2A6_000166" "g.41357306A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-975T>C" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40851401A>G" "" "likely benign" "" "0000409544" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "7160A>G" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409545" "1" "33" "19" "41349640" "41349640" "subst" "0" "00008" "CYP2A6_000021" "g.41349640G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6692C>G" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40843735G>C" "" "likely benign" "" "0000409546" "1" "33" "19" "41350664" "41350664" "subst" "0" "00008" "CYP2A6_000055" "g.41350664T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5668A" "reference haplotype CYP2A6*31B\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409547" "1" "33" "19" "41356316" "41356316" "subst" "0.00107459" "00008" "CYP2A6_000159" "g.41356316T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "16A>C" "reference haplotype CYP2A6*31B" "Germline" "" "rs72549432" "0" "" "" "g.40850411T>G" "" "likely benign" "" "0000409548" "1" "33" "19" "41354993" "41354993" "subst" "0" "00008" "CYP2A6_000132" "g.41354993G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1339C>G" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40849088G>C" "" "likely benign" "" "0000409549" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409550" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000157" "g.41356281C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G" "reference haplotype CYP2A6*31B\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 24: end of input). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409551" "1" "33" "19" "41353611" "41353611" "subst" "0" "00008" "CYP2A6_000101" "g.41353611C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2721G>A" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40847706C>T" "" "likely benign" "" "0000409552" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3225A>G" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409553" "1" "33" "19" "41353338" "41353338" "subst" "0" "00008" "CYP2A6_000099" "g.41353338A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2994T>C" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40847433A>G" "" "likely benign" "" "0000409554" "1" "33" "19" "41353017" "41353017" "subst" "0" "00008" "CYP2A6_000096" "g.41353017G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3315C>T" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40847112G>A" "" "likely benign" "" "0000409555" "1" "33" "19" "41352256" "41352256" "del" "0" "00008" "CYP2A6_000083" "g.41352256del" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "4074delA" "reference haplotype CYP2A6*31B" "Germline" "" "" "0" "" "" "g.40846351del" "" "likely benign" "" "0000409556" "1" "99" "19" "41349874" "41349874" "subst" "0" "00008" "CYP2A6_000032" "g.41349874T>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1312A>T" "reference haplotype CYP2A6*35A" "Germline" "" "rs143731390" "0" "" "" "g.40843969T>A" "" "pathogenic" "" "0000409557" "1" "33" "19" "41357344" "41357344" "subst" "0" "00008" "CYP2A6_000167" "g.41357344T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1013A>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40851439T>C" "" "likely benign" "" "0000409558" "1" "33" "19" "41357620" "41357620" "subst" "0" "00008" "CYP2A6_000172" "g.41357620C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1289G>A" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40851715C>T" "" "likely benign" "" "0000409559" "1" "33" "19" "41357632" "41357632" "subst" "0" "00008" "CYP2A6_000173" "g.41357632T>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "-1301A>C" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40851727T>G" "" "likely benign" "" "0000409560" "1" "33" "19" "41349550" "41349550" "subst" "0" "00008" "CYP2A6_000019" "g.41349550G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 6782C>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40843645G>C" "" "likely benign" "" "0000409561" "1" "33" "19" "1" "4294967295" "" "0" "00008" "CYP2A6_000007" "g.?con?" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "gene conversion in the 3\' flanking region" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000409562" "1" "33" "19" "41349172" "41349172" "subst" "0" "00008" "CYP2A6_000011" "g.41349172T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3\' CYP2A7 conversion 7160A>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40843267T>C" "" "likely benign" "" "0000409563" "1" "33" "19" "41350039" "41350039" "subst" "0" "00008" "CYP2A6_000038" "g.41350039A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6293T>C" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40844134A>G" "" "likely benign" "" "0000409564" "1" "33" "19" "41350050" "41350050" "subst" "0" "00008" "CYP2A6_000039" "g.41350050T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6282A>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40844145T>C" "" "likely benign" "" "0000409565" "1" "33" "19" "41350114" "41350114" "subst" "0" "00008" "CYP2A6_000040" "g.41350114T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6218A>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40844209T>C" "" "likely benign" "" "0000409566" "1" "33" "19" "41349978" "41349978" "subst" "0" "00008" "CYP2A6_000037" "g.41349978A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "6354T>C" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40844073A>G" "" "likely benign" "" "0000409567" "1" "33" "19" "41355612" "41355612" "subst" "0" "00008" "CYP2A6_000137" "g.41355612C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "720G>A" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40849707C>T" "" "likely benign" "" "0000409568" "1" "33" "19" "41354712" "41354712" "subst" "0.756806" "00008" "CYP2A6_000131" "g.41354712A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1620T>C" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40848807A>G" "" "likely benign" "" "0000409569" "1" "33" "19" "41355195" "41355195" "subst" "0" "00008" "CYP2A6_000135" "g.41355195G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1137C>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40849290G>C" "" "likely benign" "" "0000409570" "1" "33" "19" "41353849" "41353849" "subst" "0" "00008" "CYP2A6_000103" "g.41353849C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "2483G>A" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40847944C>T" "" "likely benign" "" "0000409571" "1" "33" "19" "41353107" "41353107" "subst" "0" "00008" "CYP2A6_000098" "g.41353107T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "3225A>G" "reference haplotype CYP2A6*35A" "Germline" "" "" "0" "" "" "g.40847202T>C" "" "likely benign" "" "0000409572" "1" "33" "19" "41351309" "41351309" "subst" "8.13074E-5" "00008" "CYP2A6_000071" "g.41351309A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1051T>C" "reference haplotype CYP2A6*38" "Germline" "" "rs148166815" "0" "" "" "g.40845404A>G" "" "likely benign" "" "0000409573" "1" "33" "19" "41350615" "41350615" "subst" "0.0305591" "00008" "CYP2A6_000051" "g.41350615G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1224C>T" "reference haplotype CYP2A6*39" "Germline" "" "" "0" "" "" "g.40844710G>A" "" "likely benign" "" "0000409574" "1" "33" "19" "41356161" "41356161" "subst" "0" "00008" "CYP2A6_000153" "g.41356161G>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "171C>A" "reference haplotype CYP2A6*39" "Germline" "" "" "0" "" "" "g.40850256G>T" "" "likely benign" "" "0000409575" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "459G>A" "reference haplotype CYP2A6*39" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409576" "1" "99" "19" "41355864" "41355864" "subst" "3.26086E-5" "00008" "CYP2A6_000145" "g.41355864C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "468G>A" "reference haplotype CYP2A6*39" "Germline" "" "rs143690364" "0" "" "" "g.40849959C>T" "" "pathogenic" "" "0000409577" "1" "33" "19" "41354553" "41354553" "subst" "0.0109527" "00008" "CYP2A6_000122" "g.41354553C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1779G>A" "reference haplotype CYP2A6*39" "Germline" "" "" "0" "" "" "g.40848648C>T" "" "likely benign" "" "0000409578" "1" "99" "19" "41354565" "41354565" "subst" "0" "00008" "CYP2A6_000123" "g.41354565G>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "447C>G" "reference haplotype CYP2A6*40" "Germline" "" "" "0" "" "" "g.40848660G>C" "" "pathogenic" "" "0000409579" "1" "33" "19" "41350602" "41350602" "subst" "0" "00008" "CYP2A6_000050" "g.41350602G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1237C>T" "reference haplotype CYP2A6*40" "Germline" "" "" "0" "" "" "g.40844697G>A" "" "likely benign" "" "0000409580" "1" "33" "19" "41352840" "41352840" "subst" "0.0642769" "00008" "CYP2A6_000091" "g.41352840G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "771C>T" "reference haplotype CYP2A6*40" "Germline" "" "" "0" "" "" "g.40846935G>A" "" "likely benign" "" "0000409581" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "5738C>T" "reference haplotype CYP2A6*40" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409582" "1" "33" "19" "41356188" "41356188" "subst" "0.0690959" "00008" "CYP2A6_000154" "g.41356188C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "144G>A" "reference haplotype CYP2A6*40" "Germline" "" "" "0" "" "" "g.40850283C>T" "" "likely benign" "" "0000409583" "1" "33" "19" "41355825" "41355825" "subst" "0.0001222" "00008" "CYP2A6_000144" "g.41355825G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "241C>T" "reference haplotype CYP2A6*41" "Germline" "" "" "0" "" "" "g.40849920G>A" "" "likely benign" "" "0000409584" "1" "99" "19" "41352817" "41352817" "subst" "0.000174868" "00008" "CYP2A6_000090" "g.41352817C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "794G>A" "reference haplotype CYP2A6*41" "Germline" "" "rs140471703" "0" "" "" "g.40846912C>T" "" "pathogenic" "" "0000409585" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*41" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409586" "1" "99" "19" "41352808" "41352808" "subst" "4.06679E-5" "00008" "CYP2A6_000089" "g.41352808A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "803T>C" "reference haplotype CYP2A6*42" "Germline" "" "" "0" "" "" "g.40846903A>G" "" "pathogenic" "" "0000409587" "1" "33" "19" "41350648" "41350648" "subst" "0.0206092" "00008" "CYP2A6_000054" "g.41350648A>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1191T>C" "reference haplotype CYP2A6*42" "Germline" "" "" "0" "" "" "g.40844743A>G" "" "likely benign" "" "0000409588" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*42" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000409589" "1" "99" "19" "41351926" "41351926" "subst" "0" "00008" "CYP2A6_000080" "g.41351926G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "908C>T" "reference haplotype CYP2A6*43" "Germline" "" "" "0" "" "" "g.40846021G>A" "" "pathogenic" "" "0000409590" "1" "99" "19" "41350587" "41350587" "subst" "0.000953359" "00008" "CYP2A6_000047" "g.41350587T>C" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1252A>G" "reference haplotype CYP2A6*44" "Germline" "" "rs28399463" "0" "" "" "g.40844682T>C" "" "pathogenic" "" "0000409591" "1" "99" "19" "41350671" "41350671" "subst" "0.000122693" "00008" "CYP2A6_000057" "g.41350671C>T" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1168G>A" "reference haplotype CYP2A6*44" "Germline" "" "rs376817657" "0" "" "" "g.40844766C>T" "" "pathogenic" "" "0000409592" "1" "99" "19" "41350582" "41350582" "subst" "0.000810789" "00008" "CYP2A6_000046" "g.41350582C>G" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1257G>C" "reference haplotype CYP2A6*44" "Germline" "" "rs8192730" "0" "" "" "g.40844677C>G" "" "pathogenic" "" "0000409593" "1" "33" "19" "41350594" "41350594" "subst" "0.0698831" "00008" "CYP2A6_000048" "g.41350594G>A" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "1245C>T" "reference haplotype CYP2A6*44" "Germline" "" "" "0" "" "" "g.40844689G>A" "" "likely benign" "" "0000409594" "1" "33" "19" "41356281" "41356281" "subst" "0" "00008" "CYP2A6_000156" "g.41356281=" "" "Reference haplotype - Human P450 (CYP) Allele Nomenclature Committee" "" "51G>A" "reference haplotype CYP2A6*44" "Germline" "" "" "0" "" "" "g.40850376=" "" "likely benign" "" "0000649992" "1" "50" "19" "41352941" "41352941" "subst" "0.00103497" "03575" "CYP2A6_000093" "g.41352941A>G" "24/2794 individuals" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "" "" "drug response; 24 heterozygous, no homozygous; {DB:CLININrs111033610}" "Germline" "" "rs111033610" "0" "" "" "g.40847036A>G" "" "VUS" "" "0000681415" "0" "30" "19" "41349888" "41349893" "del" "0" "02325" "CYP2A6_000180" "g.41349888_41349893del" "" "" "" "CYP2A6(NM_000762.6):c.1304-8_1304-3delCTCCTC" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000727373" "0" "90" "19" "41350599" "41350599" "subst" "8.13187E-6" "02329" "CYP2A6_000001" "g.41350599G>A" "" "" "" "CYP2A6(NM_000762.6):c.1240C>T (p.Q414*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0000727374" "0" "30" "19" "41354209" "41354209" "subst" "0.000979802" "01943" "CYP2A6_000182" "g.41354209C>A" "" "" "" "CYP2A6(NM_000762.5):c.569G>T (p.R190L)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000727375" "0" "50" "19" "41354521" "41354521" "subst" "0" "01943" "CYP2A6_000183" "g.41354521C>T" "" "" "" "CYP2A6(NM_000762.5):c.491G>A (p.G164D)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000866135" "0" "50" "19" "41349750" "41349750" "subst" "0" "01943" "CYP2A6_000029" "g.41349750C>A" "" "" "" "CYP2A6(NM_000762.5):c.1436G>T (p.G479V)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000983472" "0" "50" "19" "41350641" "41350641" "subst" "0" "02325" "CYP2A6_000184" "g.41350641T>A" "" "" "" "CYP2A6(NM_000762.6):c.1198A>T (p.R400*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000983473" "0" "30" "19" "41354538" "41354538" "subst" "0.000655264" "01804" "CYP2A6_000121" "g.41354538G>C" "" "" "" "CYP2A6(NM_000762.6):c.474C>G (p.(Asp158Glu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001042971" "0" "30" "19" "41355876" "41355876" "subst" "0.000287203" "01804" "CYP2A6_000185" "g.41355876G>A" "" "" "" "CYP2A6(NM_000762.6):c.190C>T (p.(Arg64Cys))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001042972" "0" "50" "19" "41355885" "41355885" "subst" "4.08313E-6" "01804" "CYP2A6_000186" "g.41355885T>A" "" "" "" "CYP2A6(NM_000762.6):c.181A>T (p.(Ile61Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" ## Variants_On_Transcripts ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Note: Only showing Variants_On_Transcript columns active for Genes CYP2A6 ## Count = 820 "{{id}}" "{{transcriptid}}" "{{effectid}}" "{{position_c_start}}" "{{position_c_start_intron}}" "{{position_c_end}}" "{{position_c_end_intron}}" "{{VariantOnTranscript/DNA}}" "{{VariantOnTranscript/RNA}}" "{{VariantOnTranscript/Protein}}" "{{VariantOnTranscript/Exon}}" "{{VariantOnTranscript/Haplotype}}" "0000248764" "00005994" "10" "1175" "0" "1175" "0" "c.1175=" "r.(=)" "p.(Tyr392=)" "" "" "0000254697" "00005994" "30" "217" "0" "217" "0" "c.217T>C" "r.(?)" "p.(Leu73=)" "" "" "0000254791" "00005994" "30" "786" "0" "786" "0" "c.786T>C" "r.(?)" "p.(Asn262=)" "" "" "0000267254" "00005994" "10" "51" "0" "51" "0" "c.51A>G" "r.(?)" "p.(Val17=)" "" "" "0000408785" "00005994" "99" "1560" "0" "8388607" "0" "c.(*75_?)con?" "r.(?)" "p.?" "" "" "0000408786" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408787" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408788" "00005994" "33" "-396" "0" "-396" "0" "c.-396G>A" "r.(=)" "p.(=)" "1" "" "0000408789" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408790" "00005994" "33" "1927" "0" "1936" "0" "c.*442_*451con?" "r.(?)" "p.?" "" "" "0000408791" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408792" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408793" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408794" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408795" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408796" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408797" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408798" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408799" "00005994" "33" "344" "-400" "344" "-400" "c.344-400C>G" "r.(?)" "p.(=)" "2i" "" "0000408800" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408801" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408802" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408803" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408804" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408805" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408806" "00005994" "33" "1304" "-157" "1304" "-157" "c.1304-157T>C" "r.(?)" "p.(=)" "7i" "" "0000408807" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408808" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408809" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408810" "00005994" "33" "-1464" "0" "-1464" "0" "c.-1464A>T" "r.(=)" "p.(=)" "1" "" "0000408811" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408812" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408813" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408814" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408815" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408816" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408817" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408818" "00005994" "33" "-1464" "0" "-1464" "0" "c.-1464A>T" "r.(=)" "p.(=)" "1" "" "0000408819" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408820" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408821" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408822" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408823" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408824" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408825" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408826" "00005994" "33" "-1464" "0" "-1464" "0" "c.-1464A>T" "r.(=)" "p.(=)" "1" "" "0000408827" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408828" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408829" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408830" "00005994" "33" "1304" "-61" "1304" "-61" "c.1304-61C>G" "r.(?)" "p.(=)" "7i" "" "0000408831" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408832" "00005994" "33" "-1013" "0" "-1013" "0" "c.-1013A>G" "r.(=)" "p.(=)" "1" "" "0000408833" "00005994" "33" "-1289" "0" "-1289" "0" "c.-1289G>A" "r.(=)" "p.(=)" "1" "" "0000408834" "00005994" "33" "-1301" "0" "-1301" "0" "c.-1301A>C" "r.(=)" "p.(=)" "1" "" "0000408835" "00005994" "33" "-1464" "0" "-1464" "0" "c.-1464A>T" "r.(=)" "p.(=)" "1" "" "0000408836" "00005994" "33" "-1579" "0" "-1579" "0" "c.-1579T>C" "r.(=)" "p.(=)" "1" "" "0000408837" "00005994" "33" "-1680" "0" "-1680" "0" "c.-1680A>G" "r.(=)" "p.(=)" "1" "" "0000408838" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408839" "00005994" "33" "1162" "-27" "1162" "-27" "c.1162-27C>T" "r.(?)" "p.(=)" "7i" "" "0000408840" "00005994" "33" "344" "-44" "344" "-44" "c.344-44T>C" "r.(?)" "p.(=)" "2i" "" "0000408841" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408842" "00005994" "33" "51" "0" "51" "0" "c.51=" "r.(?)" "p.(=)" "1" "" "0000408843" "00005994" "33" "1545" "0" "1545" "0" "c.*60C>G" "r.(=)" "p.(=)" "8" "" "0000408844" "00005994" "33" "-746" "0" "-746" "0" "c.-746A>G" "r.(=)" "p.(=)" "1" "" "0000408845" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408846" "00005994" "33" "22" "0" "22" "0" "c.22C>T" "r.(=)" "p.(=)" "1" "" "0000408847" "00005994" "33" "1636" "0" "1636" "0" "c.*151C>G" "r.(=)" "p.(=)" "8" "" "0000408848" "00005994" "33" "1789" "0" "1790" "0" "c.*304_*305insCACTT" "r.(=)" "p.(=)" "8" "" "0000408849" "00005994" "33" "-8388608" "0" "8388607" "0" "c.?con?" "r.(?)" "p.?" "" "" "0000408850" "00005994" "33" "2014" "0" "2014" "0" "c.*529A>G" "r.(=)" "p.(=)" "8" "" "0000408851" "00005994" "33" "181" "-109" "181" "-109" "c.181-109T>C" "r.(?)" "p.(=)" "1" "" "0000408852" "00005994" "33" "51" "0" "51" "0" "c.51=" "r.(?)" 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