### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = TAS2R38) # 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}}" "TAS2R38" "taste receptor, type 2, member 38" "7" "q34" "no" "NG_016141.1" "UD_132118988987" "" "http://www.LOVD.nl/TAS2R38" "" "1" "9584" "5726" "607751" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "http://databases.lovd.nl/shared/refseq/TAS2R38_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2010-04-29 00:00:00" "00006" "2016-08-08 09:19:51" "00006" "2020-06-05 17:29:26" ## 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}}" "00020774" "TAS2R38" "taste receptor, type 2, member 38" "001" "NM_176817.4" "" "NP_789787.4" "" "" "" "-84" "1059" "1002" "141673573" "141672431" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 3 "{{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" "01502" "THIOT" "tasting, henylthiocarbamide (bitter)" "AD" "171200" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "TAS2R38" "01502" ## Individuals ## Do not remove or alter this header ## ## Count = 114 "{{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}}" "00079241" "" "" "" "59" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079242" "" "" "" "39" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079243" "" "" "" "10" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079244" "" "" "" "127" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079245" "" "" "" "94" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "European" "" "00079246" "" "" "" "15" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "Asia, West" "" "00079247" "" "" "" "17" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "Asia, East" "" "00079248" "" "" "" "6" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079249" "" "" "" "6" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "European" "" "00079250" "" "" "" "1" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079251" "" "" "" "4" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079252" "" "" "" "98" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "European" "" "00079253" "" "" "" "7" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "Asia, West" "" "00079254" "" "" "" "37" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "Asia, East" "" "00079255" "" "" "" "12" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079256" "" "" "" "18" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "American, native" "" "00079257" "" "" "" "1" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079258" "" "" "" "14" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079259" "" "" "" "11" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079260" "" "" "" "3" "" "00006" "{PMID:Kim 2003:12595690}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079261" "" "" "" "1" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "United States" "" "0" "" "" "mixed" "" "00079262" "" "" "" "3" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079263" "" "" "" "62" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079264" "" "" "" "40" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079265" "" "" "" "6" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079266" "" "" "" "7" "" "00006" "{PMID:Prody 2004:15466815}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079267" "" "" "" "89" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Italy" "" "0" "" "" "Sardinia" "" "00079268" "" "" "" "105" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079269" "" "" "" "3" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079270" "" "" "" "10" "" "00006" "" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079271" "" "" "" "137" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079272" "" "" "" "55" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079273" "" "" "" "17" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079274" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Fulani" "" "00079275" "" "" "" "2" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079276" "" "" "" "7" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079277" "" "" "" "10" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079278" "" "" "" "1" "" "00006" "" "" "F;M" "" "Cameroon" "" "0" "" "" "Afro-asiatic" "" "00079279" "" "" "" "198" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079280" "" "" "" "6" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079281" "" "" "" "251" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079282" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Afro-asiatic" "" "00079283" "" "" "" "4" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079284" "" "" "" "1" "" "00006" "" "" "F;M" "" "Cameroon" "" "0" "" "" "Afro-asiatic" "" "00079285" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Nilo-Saharan" "" "00079286" "" "" "" "6" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079287" "" "" "" "3" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079288" "" "" "" "4" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "" "" "00079289" "" "" "" "27" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079290" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Nilo-Saharan" "" "00079291" "" "" "" "2" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079292" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Nilo-Saharan" "" "00079293" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Nilo-Saharan" "" "00079294" "" "" "" "335" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079295" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Nilo-Saharan" "" "00079296" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "Afro-asiatic" "" "00079297" "" "" "" "30" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya;Tanzania" "" "0" "" "" "" "" "00079298" "" "" "" "1" "" "00006" "" "" "F;M" "" "" "" "0" "" "" "European" "" "00079299" "" "" "" "28" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "European" "" "00079300" "" "" "" "11" "" "00006" "" "" "F;M" "" "" "" "0" "" "" "European" "" "00079301" "" "" "" "4" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "American" "" "00079302" "" "" "" "19" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "American" "" "00079303" "" "" "" "3" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "American" "" "00079304" "" "" "" "2" "" "00006" "" "" "F;M" "" "" "" "0" "" "" "Middle East" "" "00079305" "" "" "" "18" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "Middle East" "" "00079306" "" "" "" "20" "" "00006" "" "" "F;M" "" "" "" "0" "" "" "Middle East" "" "00079307" "" "" "" "8" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Pakistan" "" "0" "" "" "" "" "00079308" "" "" "" "7" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Pakistan" "" "0" "" "" "" "" "00079309" "" "" "" "1" "" "00006" "" "" "F;M" "" "Pakistan" "" "0" "" "" "" "" "00079310" "" "" "" "53" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "" "" "00079311" "" "" "" "81" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "Asiaa, east" "" "00079312" "" "" "" "8" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "Asiaa, east" "" "00079313" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079314" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079315" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya" "" "0" "" "" "Afro-asiatic" "" "00079316" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079317" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya" "" "0" "" "" "Nilo-Saharan" "" "00079318" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Nilo-Saharan" "" "00079319" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079320" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079321" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079322" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079323" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya" "" "0" "" "" "Afro-asiatic" "" "00079324" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Niger-Kordofanian" "" "00079325" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079326" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079327" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079328" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079329" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079330" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079331" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079332" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079333" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079334" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Afro-asiatic" "" "00079335" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Fulani" "" "00079336" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079337" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079338" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079339" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079340" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079341" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya" "" "0" "" "" "Afro-asiatic" "" "00079342" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079343" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079344" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079345" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079346" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Niger-Kordofanian" "" "00079347" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "pygmy" "" "00079348" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079349" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079350" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Kenya" "" "0" "" "" "Luo" "" "00079351" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "Cameroon" "" "0" "" "" "Niger-Kordofanian" "" "00079352" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "African" "" "00079353" "" "" "" "1" "" "00006" "{PMID:Campbell 2012:22130969}" "" "F;M" "" "" "" "0" "" "" "" "" "00079354" "" "" "" "1" "" "00006" "" "" "" "" "" "" "0" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 114 "{{individualid}}" "{{diseaseid}}" "00079241" "00000" "00079242" "01502" "00079243" "01502" "00079244" "01502" "00079245" "00198" "00079246" "00198" "00079247" "00198" "00079248" "00198" "00079249" "00198" "00079250" "00198" "00079251" "00198" "00079252" "00198" "00079253" "00198" "00079254" "00198" "00079255" "00198" "00079256" "00198" "00079257" "00198" "00079258" "00000" "00079259" "00000" "00079260" "00000" "00079261" "00000" "00079262" "00000" "00079263" "01502" "00079264" "01502" "00079265" "01502" "00079266" "00000" "00079267" "01502" "00079268" "00198" "00079269" "00198" "00079270" "00198" "00079271" "00198" "00079272" "00198" "00079273" "00198" "00079274" "00198" "00079275" "00198" "00079276" "00198" "00079277" "00198" "00079278" "00198" "00079279" "00198" "00079280" "00198" "00079281" "00198" "00079282" "00198" "00079283" "00198" "00079284" "00198" "00079285" "00198" "00079286" "00198" "00079287" "00198" "00079288" "00198" "00079289" "00198" "00079290" "00198" "00079291" "00198" "00079292" "00198" "00079293" "00198" "00079294" "00198" "00079295" "00198" "00079296" "00198" "00079297" "00198" "00079298" "00198" "00079299" "00198" "00079300" "00198" "00079301" "00198" "00079302" "00198" "00079303" "00198" "00079304" "00198" "00079305" "00198" "00079306" "00198" "00079307" "00198" "00079308" "00198" "00079309" "00198" "00079310" "00198" "00079311" "00198" "00079312" "00198" "00079313" "00198" "00079314" "00198" "00079315" "00198" "00079316" "00198" "00079317" "00198" "00079318" "00198" "00079319" "00198" "00079320" "00198" "00079321" "00198" "00079322" "00198" "00079323" "00198" "00079324" "00198" "00079325" "00198" "00079326" "00198" "00079327" "00198" "00079328" "00198" "00079329" "00198" "00079330" "00198" "00079331" "00198" "00079332" "00198" "00079333" "00198" "00079334" "00198" "00079335" "00198" "00079336" "00198" "00079337" "00198" "00079338" "00198" "00079339" "00198" "00079340" "00198" "00079341" "00198" "00079342" "00198" "00079343" "00198" "00079344" "00198" "00079345" "00198" "00079346" "00198" "00079347" "00198" "00079348" "00198" "00079349" "00198" "00079350" "00198" "00079351" "00198" "00079352" "00198" "00079353" "00198" "00079354" "00198" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00000, 00198, 01502 ## Count = 114 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Tumor/MSI}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "{{Phenotype/Diagnosis/Criteria}}" "0000058969" "00000" "00079241" "00006" "Familial, autosomal recessive" "" "not tasting bitter (no PTC sensitivity), PTC score 4.31/1.86" "" "" "" "" "" "" "" "" "" "" "" "0000058970" "01502" "00079242" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive), PTC score 10.69/10.00" "" "" "" "" "" "" "" "" "" "" "" "0000058971" "01502" "00079243" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive)" "" "" "" "" "" "" "" "" "" "" "" "0000058972" "01502" "00079244" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive), PTC score 9.65/8.81" "" "" "" "" "" "" "" "" "" "" "" "0000058973" "00198" "00079245" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058974" "00198" "00079246" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058975" "00198" "00079247" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058976" "00198" "00079248" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058977" "00198" "00079249" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058978" "00198" "00079250" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058979" "00198" "00079251" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058980" "00198" "00079252" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058981" "00198" "00079253" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058982" "00198" "00079254" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058983" "00198" "00079255" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058984" "00198" "00079256" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058985" "00198" "00079257" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058986" "00000" "00079258" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058987" "00000" "00079259" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058988" "00000" "00079260" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058989" "00000" "00079261" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058990" "00000" "00079262" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058991" "01502" "00079263" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive)" "" "" "" "" "" "" "" "" "" "" "" "0000058992" "01502" "00079264" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive)" "" "" "" "" "" "" "" "" "" "" "" "0000058993" "01502" "00079265" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive)" "" "" "" "" "" "" "" "" "" "" "" "0000058994" "00000" "00079266" "00006" "Familial, autosomal dominant" "" "not tasting bitter (no PTC sensitivity)" "" "" "" "" "" "" "" "" "" "" "" "0000058995" "01502" "00079267" "00006" "Familial, autosomal dominant" "" "taste, bitter (PTC sensitive)" "" "" "" "" "" "" "" "" "" "" "" "0000058996" "00198" "00079268" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058997" "00198" "00079269" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058998" "00198" "00079270" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000058999" "00198" "00079271" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059000" "00198" "00079272" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059001" "00198" "00079273" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059002" "00198" "00079274" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059003" "00198" "00079275" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059004" "00198" "00079276" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059005" "00198" "00079277" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059006" "00198" "00079278" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059007" "00198" "00079279" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059008" "00198" "00079280" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059009" "00198" "00079281" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059010" "00198" "00079282" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059011" "00198" "00079283" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059012" "00198" "00079284" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059013" "00198" "00079285" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059014" "00198" "00079286" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059015" "00198" "00079287" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059016" "00198" "00079288" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059017" "00198" "00079289" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059018" "00198" "00079290" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059019" "00198" "00079291" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059020" "00198" "00079292" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059021" "00198" "00079293" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059022" "00198" "00079294" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059023" "00198" "00079295" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059024" "00198" "00079296" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059025" "00198" "00079297" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059026" "00198" "00079298" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059027" "00198" "00079299" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059028" "00198" "00079300" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059029" "00198" "00079301" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059030" "00198" "00079302" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059031" "00198" "00079303" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059032" "00198" "00079304" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059033" "00198" "00079305" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059034" "00198" "00079306" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059035" "00198" "00079307" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059036" "00198" "00079308" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059037" "00198" "00079309" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059038" "00198" "00079310" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059039" "00198" "00079311" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059040" "00198" "00079312" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059041" "00198" "00079313" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059042" "00198" "00079314" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059043" "00198" "00079315" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059044" "00198" "00079316" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059045" "00198" "00079317" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059046" "00198" "00079318" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059047" "00198" "00079319" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059048" "00198" "00079320" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059049" "00198" "00079321" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059050" "00198" "00079322" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059051" "00198" "00079323" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059052" "00198" "00079324" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059053" "00198" "00079325" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059054" "00198" "00079326" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059055" "00198" "00079327" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059056" "00198" "00079328" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059057" "00198" "00079329" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059058" "00198" "00079330" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059059" "00198" "00079331" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059060" "00198" "00079332" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059061" "00198" "00079333" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059062" "00198" "00079334" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059063" "00198" "00079335" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059064" "00198" "00079336" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059065" "00198" "00079337" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059066" "00198" "00079338" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059067" "00198" "00079339" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059068" "00198" "00079340" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059069" "00198" "00079341" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059070" "00198" "00079342" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059071" "00198" "00079343" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059072" "00198" "00079344" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059073" "00198" "00079345" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059074" "00198" "00079346" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059075" "00198" "00079347" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059076" "00198" "00079348" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059077" "00198" "00079349" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059078" "00198" "00079350" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059079" "00198" "00079351" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059080" "00198" "00079352" "00006" "Unknown" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059081" "00198" "00079353" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" "0000059082" "00198" "00079354" "00006" "Familial, autosomal dominant" "" "untested bitter tasting" "" "" "" "" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 114 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000079313" "00079241" "1" "00006" "00006" "2012-10-21 12:09:11" "00006" "2012-10-21 12:40:34" "SEQ" "DNA" "" "" "0000079314" "00079242" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079315" "00079243" "1" "00006" "00006" "2012-10-21 12:09:11" "00006" "2012-10-21 12:47:22" "SEQ" "DNA" "" "" "0000079316" "00079244" "1" "00006" "00006" "2012-10-21 12:09:11" "00006" "2012-10-21 13:04:54" "SEQ" "DNA" "" "" "0000079317" "00079245" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079318" "00079246" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079319" "00079247" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079320" "00079248" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079321" "00079249" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079322" "00079250" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079323" "00079251" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079324" "00079252" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079325" "00079253" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079326" "00079254" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079327" "00079255" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079328" "00079256" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079329" "00079257" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079330" "00079258" "1" "00006" "00006" "2012-10-21 12:09:11" "00006" "2012-10-21 12:40:34" "SEQ" "DNA" "" "" "0000079331" "00079259" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079332" "00079260" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079333" "00079261" "1" "00006" "00006" "2012-10-21 12:09:11" "" "" "SEQ" "DNA" "" "" "0000079334" "00079262" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079335" "00079263" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079336" "00079264" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079337" "00079265" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079338" "00079266" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079339" "00079267" "1" "00006" "00006" "2012-10-21 14:01:01" "" "" "SEQ" "DNA" "" "" "0000079340" "00079268" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079341" "00079269" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079342" "00079270" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079343" "00079271" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079344" "00079272" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079345" "00079273" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079346" "00079274" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079347" "00079275" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079348" "00079276" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079349" "00079277" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079350" "00079278" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079351" "00079279" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079352" "00079280" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079353" "00079281" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079354" "00079282" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079355" "00079283" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079356" "00079284" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079357" "00079285" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079358" "00079286" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079359" "00079287" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079360" "00079288" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079361" "00079289" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079362" "00079290" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079363" "00079291" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079364" "00079292" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079365" "00079293" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079366" "00079294" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079367" "00079295" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079368" "00079296" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079369" "00079297" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079370" "00079298" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079371" "00079299" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079372" "00079300" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079373" "00079301" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079374" "00079302" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079375" "00079303" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079376" "00079304" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079377" "00079305" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079378" "00079306" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079379" "00079307" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079380" "00079308" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079381" "00079309" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079382" "00079310" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079383" "00079311" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079384" "00079312" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079385" "00079313" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079386" "00079314" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079387" "00079315" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079388" "00079316" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079389" "00079317" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079390" "00079318" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079391" "00079319" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079392" "00079320" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079393" "00079321" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079394" "00079322" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079395" "00079323" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079396" "00079324" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079397" "00079325" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079398" "00079326" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079399" "00079327" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079400" "00079328" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079401" "00079329" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079402" "00079330" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079403" "00079331" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079404" "00079332" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079405" "00079333" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079406" "00079334" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079407" "00079335" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079408" "00079336" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079409" "00079337" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079410" "00079338" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079411" "00079339" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079412" "00079340" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079413" "00079341" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079414" "00079342" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079415" "00079343" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079416" "00079344" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079417" "00079345" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079418" "00079346" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079419" "00079347" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079420" "00079348" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079421" "00079349" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079422" "00079350" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079423" "00079351" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079424" "00079352" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079425" "00079353" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" "0000079426" "00079354" "1" "00006" "00006" "2012-11-19 19:52:56" "" "" "SEQ" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 114 "{{screeningid}}" "{{geneid}}" "0000079313" "TAS2R38" "0000079314" "TAS2R38" "0000079315" "TAS2R38" "0000079316" "TAS2R38" "0000079317" "TAS2R38" "0000079318" "TAS2R38" "0000079319" "TAS2R38" "0000079320" "TAS2R38" "0000079321" "TAS2R38" "0000079322" "TAS2R38" "0000079323" "TAS2R38" "0000079324" "TAS2R38" "0000079325" "TAS2R38" "0000079326" "TAS2R38" "0000079327" "TAS2R38" "0000079328" "TAS2R38" "0000079329" "TAS2R38" "0000079330" "TAS2R38" "0000079331" "TAS2R38" "0000079332" "TAS2R38" "0000079333" "TAS2R38" "0000079334" "TAS2R38" "0000079335" "TAS2R38" "0000079336" "TAS2R38" "0000079337" "TAS2R38" "0000079338" "TAS2R38" "0000079339" "TAS2R38" "0000079340" "TAS2R38" "0000079341" "TAS2R38" "0000079342" "TAS2R38" "0000079343" "TAS2R38" "0000079344" "TAS2R38" "0000079345" "TAS2R38" "0000079346" "TAS2R38" "0000079347" "TAS2R38" "0000079348" "TAS2R38" "0000079349" "TAS2R38" "0000079350" "TAS2R38" "0000079351" "TAS2R38" "0000079352" "TAS2R38" "0000079353" "TAS2R38" "0000079354" "TAS2R38" "0000079355" "TAS2R38" "0000079356" "TAS2R38" "0000079357" "TAS2R38" "0000079358" "TAS2R38" "0000079359" "TAS2R38" "0000079360" "TAS2R38" "0000079361" "TAS2R38" "0000079362" "TAS2R38" "0000079363" "TAS2R38" "0000079364" "TAS2R38" "0000079365" "TAS2R38" "0000079366" "TAS2R38" "0000079367" "TAS2R38" "0000079368" "TAS2R38" "0000079369" "TAS2R38" "0000079370" "TAS2R38" "0000079371" "TAS2R38" "0000079372" "TAS2R38" "0000079373" "TAS2R38" "0000079374" "TAS2R38" "0000079375" "TAS2R38" "0000079376" "TAS2R38" "0000079377" "TAS2R38" "0000079378" "TAS2R38" "0000079379" "TAS2R38" "0000079380" "TAS2R38" "0000079381" "TAS2R38" "0000079382" "TAS2R38" "0000079383" "TAS2R38" "0000079384" "TAS2R38" "0000079385" "TAS2R38" "0000079386" "TAS2R38" "0000079387" "TAS2R38" "0000079388" "TAS2R38" "0000079389" "TAS2R38" "0000079390" "TAS2R38" "0000079391" "TAS2R38" "0000079392" "TAS2R38" "0000079393" "TAS2R38" "0000079394" "TAS2R38" "0000079395" "TAS2R38" "0000079396" "TAS2R38" "0000079397" "TAS2R38" "0000079398" "TAS2R38" "0000079399" "TAS2R38" "0000079400" "TAS2R38" "0000079401" "TAS2R38" "0000079402" "TAS2R38" "0000079403" "TAS2R38" "0000079404" "TAS2R38" "0000079405" "TAS2R38" "0000079406" "TAS2R38" "0000079407" "TAS2R38" "0000079408" "TAS2R38" "0000079409" "TAS2R38" "0000079410" "TAS2R38" "0000079411" "TAS2R38" "0000079412" "TAS2R38" "0000079413" "TAS2R38" "0000079414" "TAS2R38" "0000079415" "TAS2R38" "0000079416" "TAS2R38" "0000079417" "TAS2R38" "0000079418" "TAS2R38" "0000079419" "TAS2R38" "0000079420" "TAS2R38" "0000079421" "TAS2R38" "0000079422" "TAS2R38" "0000079423" "TAS2R38" "0000079424" "TAS2R38" "0000079425" "TAS2R38" "0000079426" "TAS2R38" ## 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 = 201 "{{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}}" "0000127952" "3" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "59/73 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127953" "3" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "39/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127954" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "10/21 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127955" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "127/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127956" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "94/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127957" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "15/22" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127958" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "17/54" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127959" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "6/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127960" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "6/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127961" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127962" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "4/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127963" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "98/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127964" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "7/22" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127965" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "37/54" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127966" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "12/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127967" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "18/18" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127968" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127969" "3" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "14/73 cases" "{PMID:Kim 2003:12595690}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127970" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "11/21 cases" "{PMID:Kim 2003:12595690}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127971" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "3/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127972" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "AAV haplotype; evolutionary original" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000127973" "3" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "3/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127974" "3" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "62/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127975" "3" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "40/46" "{PMID:Prody 2004:15466815}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127976" "3" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "6/46" "{PMID:Prody 2004:15466815}" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127977" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "7/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127978" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "89/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127979" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "105/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127980" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "3/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127981" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "10/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127982" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127983" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "55/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127984" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "17/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127985" "1" "50" "7" "141672681" "141672681" "subst" "0" "00006" "TAS2R38_000020" "g.141672681A>C" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1808T>G" "" "Germline" "" "" "0" "" "" "g.141972881A>C" "" "VUS" "" "0000127986" "1" "50" "7" "141672841" "141672841" "subst" "4.87698E-5" "00006" "TAS2R38_000021" "g.141672841T>G" "2/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1648A>C" "" "Germline" "" "" "0" "" "" "g.141973041T>G" "" "VUS" "" "0000127987" "1" "50" "7" "141673087" "141673087" "subst" "0.000600372" "00006" "TAS2R38_000014" "g.141673087A>C" "7/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1402T>G" "" "Germline" "" "" "0" "" "" "g.141973287A>C" "" "VUS" "" "0000127988" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "10/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127989" "1" "50" "7" "141673251" "141673251" "subst" "0.000199138" "00006" "TAS2R38_000006" "g.141673251T>C" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1238A>G" "" "Germline" "" "" "0" "" "" "g.141973451T>C" "" "VUS" "" "0000127990" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127991" "1" "50" "7" "141673299" "141673299" "subst" "0.000369853" "00006" "TAS2R38_000007" "g.141673299C>T" "6/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1190G>A" "" "Germline" "" "" "0" "" "" "g.141973499C>T" "" "VUS" "" "0000127992" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127993" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127994" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "4/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127995" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000127996" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000127997" "1" "50" "7" "141673384" "141673384" "subst" "0.000337256" "00006" "TAS2R38_000012" "g.141673384C>T" "6/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1105G>A" "" "Germline" "" "" "0" "" "" "g.141973584C>T" "" "VUS" "" "0000127998" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "3/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000127999" "1" "50" "7" "141673473" "141673473" "subst" "0.000167715" "00006" "TAS2R38_000013" "g.141673473C>T" "4/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1016G>A" "" "Germline" "" "" "0" "" "" "g.141973673C>T" "" "VUS" "" "0000128000" "1" "50" "7" "141673087" "141673087" "subst" "0.000600372" "00006" "TAS2R38_000014" "g.141673087A>C" "27/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1402T>G" "" "Germline" "" "" "0" "" "" "g.141973287A>C" "" "VUS" "" "0000128001" "1" "50" "7" "141673128" "141673128" "subst" "0" "00006" "TAS2R38_000015" "g.141673128A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1361T>C" "" "Germline" "" "" "0" "" "" "g.141973328A>G" "" "VUS" "" "0000128002" "1" "50" "7" "141673251" "141673251" "subst" "0.000199138" "00006" "TAS2R38_000006" "g.141673251T>C" "2/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1238A>G" "" "Germline" "" "" "0" "" "" "g.141973451T>C" "" "VUS" "" "0000128003" "1" "50" "7" "141673251" "141673251" "subst" "0.000199138" "00006" "TAS2R38_000006" "g.141673251T>C" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1238A>G" "" "Germline" "" "" "0" "" "" "g.141973451T>C" "" "VUS" "" "0000128004" "1" "50" "7" "141673299" "141673299" "subst" "0.000369853" "00006" "TAS2R38_000007" "g.141673299C>T" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1190G>A" "" "Germline" "" "" "0" "" "" "g.141973499C>T" "" "VUS" "" "0000128005" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "335/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128006" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128007" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128008" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "30/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128009" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128010" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000128011" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "11/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128012" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000128013" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "19/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128014" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "3/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128015" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "2/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128016" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000128017" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "20/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128018" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000128019" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "7/16 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128020" "1" "50" "7" "141672668" "141672668" "subst" "0.000960458" "00006" "TAS2R38_000019" "g.141672668G>A" "1/16 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1821C>T (R274R(" "" "Germline" "" "" "0" "" "" "g.141972868G>A" "" "VUS" "" "0000128021" "1" "10" "7" "0" "0" "subst" "0" "00006" "TAS2R38_000000" "g.=" "127/170 cases" "" "" "" "normal chromosome; AVI haplotype\r\nVariant Error [ESYNTAX]: This genomic variant has an error (char 15: expected one of \'(\', \'?\', or a digit). Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "" "" "benign (recessive)" "" "0000128022" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "81/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128023" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "8/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128024" "1" "50" "7" "141674481" "141674481" "subst" "0" "00006" "TAS2R38_000022" "g.141674481T>C" "0.048" "{PMID:Campbell 2012:22130969}" "" "8A>G" "" "Germline" "" "" "0" "" "" "g.141974681T>C" "" "VUS" "" "0000128025" "1" "50" "7" "141674415" "141674415" "subst" "0" "00006" "TAS2R38_000023" "g.141674415T>G" "0.048" "{PMID:Campbell 2012:22130969}" "" "74A>C" "" "Germline" "" "" "0" "" "" "g.141974615T>G" "" "VUS" "" "0000128026" "1" "50" "7" "141674413" "141674413" "subst" "0" "00006" "TAS2R38_000024" "g.141674413C>G" "0.004" "{PMID:Campbell 2012:22130969}" "" "76G>C" "" "Germline" "" "" "0" "" "" "g.141974613C>G" "" "VUS" "" "0000128027" "1" "50" "7" "141674387" "141674387" "subst" "0" "00006" "TAS2R38_000025" "g.141674387G>A" "0.017" "{PMID:Campbell 2012:22130969}" "" "102C>T" "" "Germline" "" "" "0" "" "" "g.141974587G>A" "" "VUS" "" "0000128028" "1" "50" "7" "141674342" "141674342" "subst" "0" "00006" "TAS2R38_000026" "g.141674342G>A" "0.012" "{PMID:Campbell 2012:22130969}" "" "147C>T" "" "Germline" "" "" "0" "" "" "g.141974542G>A" "" "VUS" "" "0000128029" "1" "50" "7" "141674337" "141674337" "subst" "0" "00006" "TAS2R38_000027" "g.141674337G>A" "0.019" "{PMID:Campbell 2012:22130969}" "" "152C>T" "" "Germline" "" "" "0" "" "" "g.141974537G>A" "" "VUS" "" "0000128030" "1" "50" "7" "141674316" "141674316" "subst" "0" "00006" "TAS2R38_000028" "g.141674316T>C" "0.001" "{PMID:Campbell 2012:22130969}" "" "173A>G" "" "Germline" "" "" "0" "" "" "g.141974516T>C" "" "VUS" "" "0000128031" "1" "50" "7" "141674306" "141674306" "subst" "0" "00006" "TAS2R38_000029" "g.141674306G>C" "0.001" "{PMID:Campbell 2012:22130969}" "" "183C>G" "" "Germline" "" "" "0" "" "" "g.141974506G>C" "" "VUS" "" "0000128032" "1" "50" "7" "141674181" "141674181" "subst" "0" "00006" "TAS2R38_000030" "g.141674181T>C" "0.016" "{PMID:Campbell 2012:22130969}" "" "308A>G" "" "Germline" "" "" "0" "" "" "g.141974381T>C" "" "VUS" "" "0000128033" "1" "50" "7" "141674146" "141674146" "subst" "0" "00006" "TAS2R38_000031" "g.141674146T>A" "0.048" "{PMID:Campbell 2012:22130969}" "" "343A>T" "" "Germline" "" "" "0" "" "" "g.141974346T>A" "" "VUS" "" "0000128034" "1" "50" "7" "141674104" "141674104" "subst" "0" "00006" "TAS2R38_000032" "g.141674104C>T" "0.008" "{PMID:Campbell 2012:22130969}" "" "385G>A" "" "Germline" "" "" "0" "" "" "g.141974304C>T" "" "VUS" "" "0000128035" "1" "50" "7" "141674097" "141674097" "subst" "0" "00006" "TAS2R38_000033" "g.141674097A>T" "0.024" "{PMID:Campbell 2012:22130969}" "" "392T>A" "" "Germline" "" "" "0" "" "" "g.141974297A>T" "" "VUS" "" "0000128036" "1" "50" "7" "141674096" "141674096" "subst" "0" "00006" "TAS2R38_000034" "g.141674096T>A" "0.038" "{PMID:Campbell 2012:22130969}" "" "393A>T" "" "Germline" "" "rs75675140" "0" "" "" "g.141974296T>A" "" "VUS" "" "0000128037" "1" "50" "7" "141674067" "141674067" "subst" "0" "00006" "TAS2R38_000035" "g.141674067A>C" "0.078" "{PMID:Campbell 2012:22130969}" "" "422T>G" "" "Germline" "" "rs61464348" "0" "" "" "g.141974267A>C" "" "VUS" "" "0000128038" "1" "50" "7" "141674061" "141674061" "subst" "0" "00006" "TAS2R38_000036" "g.141674061T>C" "0.021" "{PMID:Campbell 2012:22130969}" "" "428A>G" "" "Germline" "" "" "0" "" "" "g.141974261T>C" "" "VUS" "" "0000128039" "1" "50" "7" "141674041" "141674041" "subst" "0" "00006" "TAS2R38_000037" "g.141674041C>T" "0.008" "{PMID:Campbell 2012:22130969}" "" "448G>A" "" "Germline" "" "" "0" "" "" "g.141974241C>T" "" "VUS" "" "0000128040" "1" "50" "7" "141673965" "141673965" "subst" "0" "00006" "TAS2R38_000038" "g.141673965T>C" "0.001" "{PMID:Campbell 2012:22130969}" "" "524A>G" "" "Germline" "" "" "0" "" "" "g.141974165T>C" "" "VUS" "" "0000128041" "1" "50" "7" "141673903" "141673903" "subst" "0" "00006" "TAS2R38_000039" "g.141673903C>T" "0.048" "{PMID:Campbell 2012:22130969}" "" "586G>A" "" "Germline" "" "" "0" "" "" "g.141974103C>T" "" "VUS" "" "0000128042" "1" "50" "7" "141673833" "141673833" "subst" "0" "00006" "TAS2R38_000040" "g.141673833G>A" "0.005" "{PMID:Campbell 2012:22130969}" "" "656C>T" "" "Germline" "" "" "0" "" "" "g.141974033G>A" "" "VUS" "" "0000128043" "1" "50" "7" "141673808" "141673808" "subst" "0" "00006" "TAS2R38_000041" "g.141673808C>G" "0.038" "{PMID:Campbell 2012:22130969}" "" "681G>C" "" "Germline" "" "" "0" "" "" "g.141974008C>G" "" "VUS" "" "0000128044" "1" "50" "7" "141673722" "141673722" "subst" "0" "00006" "TAS2R38_000042" "g.141673722C>A" "0.048" "{PMID:Campbell 2012:22130969}" "" "767G>T" "" "Germline" "" "" "0" "" "" "g.141973922C>A" "" "VUS" "" "0000128045" "1" "50" "7" "141673721" "141673721" "subst" "0" "00006" "TAS2R38_000043" "g.141673721G>A" "0.007" "{PMID:Campbell 2012:22130969}" "" "768C>T" "" "Germline" "" "" "0" "" "" "g.141973921G>A" "" "VUS" "" "0000128046" "1" "50" "7" "141673714" "141673714" "subst" "0" "00006" "TAS2R38_000044" "g.141673714C>T" "0.01" "{PMID:Campbell 2012:22130969}" "" "775G>A" "" "Germline" "" "" "0" "" "" "g.141973914C>T" "" "VUS" "" "0000128047" "1" "50" "7" "141673669" "141673669" "subst" "0" "00006" "TAS2R38_000045" "g.141673669G>A" "0.001" "{PMID:Campbell 2012:22130969}" "" "820C>T" "" "Germline" "" "" "0" "" "" "g.141973869G>A" "" "VUS" "" "0000128048" "1" "50" "7" "141673650" "141673650" "subst" "0" "00006" "TAS2R38_000046" "g.141673650G>A" "0.001" "{PMID:Campbell 2012:22130969}" "" "839C>T" "" "Germline" "" "" "0" "" "" "g.141973850G>A" "" "VUS" "" "0000128049" "1" "50" "7" "141673646" "141673646" "subst" "0" "00006" "TAS2R38_000047" "g.141673646G>A" "0.015" "{PMID:Campbell 2012:22130969}" "" "843C>T" "" "Germline" "" "rs80134535" "0" "" "" "g.141973846G>A" "" "VUS" "" "0000128050" "1" "50" "7" "141673634" "141673634" "subst" "0" "00006" "TAS2R38_000048" "g.141673634C>G" "0.017" "{PMID:Campbell 2012:22130969}" "" "855G>C" "" "Germline" "" "" "0" "" "" "g.141973834C>G" "" "VUS" "" "0000128051" "1" "50" "7" "141673582" "141673582" "subst" "0" "00006" "TAS2R38_000049" "g.141673582C>T" "0.008" "{PMID:Campbell 2012:22130969}" "" "907G>A" "" "Germline" "" "" "0" "" "" "g.141973782C>T" "" "VUS" "" "0000128052" "1" "50" "7" "141673548" "141673548" "subst" "0" "00006" "TAS2R38_000050" "g.141673548C>T" "0.004" "{PMID:Campbell 2012:22130969}" "" "941G>A" "" "Germline" "" "" "0" "" "" "g.141973748C>T" "" "VUS" "" "0000128053" "1" "50" "7" "141672477" "141672477" "subst" "8.64536E-6" "00006" "TAS2R38_000051" "g.141672477C>T" "0.032" "{PMID:Campbell 2012:22130969}" "" "2012G>A" "" "Germline" "" "" "0" "" "" "g.141972677C>T" "" "VUS" "" "0000128054" "1" "50" "7" "141672370" "141672370" "subst" "0" "00006" "TAS2R38_000052" "g.141672370C>T" "0.003" "{PMID:Campbell 2012:22130969}" "" "2119A>G" "Variant Error [EREF/ERANGE]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message." "Germline" "" "" "0" "" "" "g.141972570C>T" "" "VUS" "" "0000128055" "1" "50" "7" "141672079" "141672079" "subst" "0" "00006" "TAS2R38_000053" "g.141672079G>C" "0.016" "{PMID:Campbell 2012:22130969}" "" "2410C>G" "" "Germline" "" "" "0" "" "" "g.141972279G>C" "" "VUS" "" "0000128056" "1" "50" "7" "141672058" "141672058" "subst" "0" "00006" "TAS2R38_000054" "g.141672058G>A" "0.023" "{PMID:Campbell 2012:22130969}" "" "2431C>T" "" "Germline" "" "rs73740218" "0" "" "" "g.141972258G>A" "" "VUS" "" "0000128057" "1" "50" "7" "141671981" "141671981" "subst" "0" "00006" "TAS2R38_000055" "g.141671981A>G" "0.008" "{PMID:Campbell 2012:22130969}" "" "2508T>C" "" "Germline" "" "" "0" "" "" "g.141972181A>G" "" "VUS" "" "0000128058" "1" "50" "7" "141671875" "141671875" "subst" "0" "00006" "TAS2R38_000056" "g.141671875A>C" "0.048" "{PMID:Campbell 2012:22130969}" "" "2614T>G" "" "Germline" "" "" "0" "" "" "g.141972075A>C" "" "VUS" "" "0000128059" "1" "50" "7" "141671802" "141671802" "subst" "0" "00006" "TAS2R38_000057" "g.141671802A>G" "0.001" "{PMID:Campbell 2012:22130969}" "" "2687T>C" "" "Germline" "" "" "0" "" "" "g.141972002A>G" "" "VUS" "" "0000128060" "1" "50" "7" "141671617" "141671617" "subst" "0" "00006" "TAS2R38_000058" "g.141671617G>A" "0.04" "{PMID:Campbell 2012:22130969}" "" "2872C>T" "" "Germline" "" "rs73540580" "0" "" "" "g.141971817G>A" "" "VUS" "" "0000128061" "1" "50" "7" "141671604" "141671604" "subst" "0" "00006" "TAS2R38_000059" "g.141671604C>T" "0.001" "{PMID:Campbell 2012:22130969}" "" "2885G>A" "" "Germline" "" "" "0" "" "" "g.141971804C>T" "" "VUS" "" "0000128062" "1" "50" "7" "141671562" "141671562" "subst" "0" "00006" "TAS2R38_000060" "g.141671562G>A" "0.008" "{PMID:Campbell 2012:22130969}" "" "2927C>T" "" "Germline" "" "" "0" "" "" "g.141971762G>A" "" "VUS" "" "0000128063" "1" "50" "7" "141671556" "141671556" "subst" "0" "00006" "TAS2R38_000061" "g.141671556A>G" "0.001" "{PMID:Campbell 2012:22130969}" "" "2933T>C" "" "Germline" "" "" "0" "" "" "g.141971756A>G" "" "VUS" "" "0000128064" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "" "variant originated ago ~1.5My" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128065" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "" "variant originated ago ~0.9My" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128066" "3" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "39/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128067" "3" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "39/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128068" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "10/21 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128069" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "127/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128070" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "127/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128071" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "6/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128072" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128073" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "98/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128074" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "98/200" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128075" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "7/22" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128076" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "7/22" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128077" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "37/54" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128078" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "37/54" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128079" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "12/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128080" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "12/24" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128081" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "18/18" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128082" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "18/18" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128083" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "11/21 cases" "{PMID:Kim 2003:12595690}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128084" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "3/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128085" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "3/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128086" "2" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "1/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0001}" "" "" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128087" "3" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0002}" "" "" "AAV haplotype; evolutionary original\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128088" "2" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/170 cases" "{PMID:Kim 2003:12595690}, {OMIM607751:0003}" "" "" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128089" "3" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "3/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128090" "3" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "3/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128091" "3" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "62/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128092" "3" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "62/65" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128093" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "7/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128094" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "7/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128095" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "89/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128096" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "89/96" "{PMID:Prody 2004:15466815}" "" "" "PAV haplotype; evolutionary original" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128097" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "3/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128098" "1" "50" "7" "141672670" "141672670" "subst" "0.00137554" "00006" "TAS2R38_000005" "g.141672670G>A" "10/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1819C>T" "" "Germline" "" "" "0" "" "" "g.141972870G>A" "" "VUS" "" "0000128099" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "17/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128100" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "7/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128101" "1" "50" "7" "141672670" "141672670" "subst" "0.00137554" "00006" "TAS2R38_000005" "g.141672670G>A" "10/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1819C>T" "" "Germline" "" "" "0" "" "" "g.141972870G>A" "" "VUS" "" "0000128102" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128103" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128104" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128105" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128106" "1" "50" "7" "141672688" "141672688" "subst" "2.44151E-5" "00006" "TAS2R38_000008" "g.141672688G>A" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1801C>T" "" "Germline" "" "" "0" "" "" "g.141972888G>A" "" "VUS" "" "0000128107" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128108" "1" "50" "7" "141672786" "141672786" "subst" "8.12585E-5" "00006" "TAS2R38_000009" "g.141672786C>T" "4/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1703G>A" "" "Germline" "" "" "0" "" "" "g.141972986C>T" "" "VUS" "" "0000128109" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "4/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128110" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "4/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128111" "1" "50" "7" "141672921" "141672921" "subst" "0.000648519" "00006" "TAS2R38_000010" "g.141672921T>C" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1568A>G" "" "Germline" "" "" "0" "" "" "g.141973121T>C" "" "VUS" "" "0000128112" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128113" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128114" "1" "50" "7" "141672558" "141672558" "subst" "0" "00006" "TAS2R38_000011" "g.141672558A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1931T>C" "" "Germline" "" "" "0" "" "" "g.141972758A>G" "" "VUS" "" "0000128115" "1" "70" "7" "141673345" "141673345" "subst" "0.456251" "00006" "TAS2R38_000001" "g.141673345C>G" "6/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1144C>G" "" "Germline" "" "rs713598" "0" "" "" "g.141973545C>G" "" "likely benign (dominant)" "" "0000128116" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "6/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128117" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "6/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128118" "1" "50" "7" "141673397" "141673397" "subst" "0.000203163" "00006" "TAS2R38_000004" "g.141673397C>T" "3/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1092G>A (L31L)" "" "Germline" "" "" "0" "" "" "g.141973597C>T" "" "VUS" "" "0000128119" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "27/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128120" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128121" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "2/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128122" "1" "50" "7" "141673122" "141673122" "subst" "8.15255E-6" "00006" "TAS2R38_000016" "g.141673122C>T" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1367G>A" "" "Germline" "" "" "0" "" "" "g.141973322C>T" "" "VUS" "" "0000128123" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128124" "1" "50" "7" "141672667" "141672667" "subst" "4.47679E-5" "00006" "TAS2R38_000017" "g.141672667C>T" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1822G>A" "" "Germline" "" "" "0" "" "" "g.141972867C>T" "" "VUS" "" "0000128125" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "335/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128126" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "335/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128127" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128128" "1" "50" "7" "141672688" "141672688" "subst" "2.44151E-5" "00006" "TAS2R38_000008" "g.141672688G>A" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1801C>T" "" "Germline" "" "" "0" "" "" "g.141972888G>A" "" "VUS" "" "0000128129" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128130" "1" "50" "7" "141672786" "141672786" "subst" "8.12585E-5" "00006" "TAS2R38_000009" "g.141672786C>T" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1703G>A" "" "Germline" "" "" "0" "" "" "g.141972986C>T" "" "VUS" "" "0000128131" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128132" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "1/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128133" "1" "50" "7" "141672921" "141672921" "subst" "0.000648519" "00006" "TAS2R38_000010" "g.141672921T>C" "30/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1568A>G" "" "Germline" "" "" "0" "" "" "g.141973121T>C" "" "VUS" "" "0000128134" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "30/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128135" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "30/680 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128136" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "11/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128137" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "11/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128138" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "19/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128139" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "19/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128140" "1" "50" "7" "141673074" "141673074" "subst" "0.0123195" "00006" "TAS2R38_000018" "g.141673074T>C" "3/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1415A>G" "" "Germline" "" "" "0" "" "" "g.141973274T>C" "" "VUS" "" "0000128141" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "3/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128142" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "3/26 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128143" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "20/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128144" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "20/40 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128145" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "7/16 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128146" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "7/16 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128147" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "81/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128148" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "81/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128149" "1" "50" "7" "141673074" "141673074" "subst" "0.0123195" "00006" "TAS2R38_000018" "g.141673074T>C" "8/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1415A>G" "" "Germline" "" "" "0" "" "" "g.141973274T>C" "" "VUS" "" "0000128150" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "8/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1784C>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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" "0000128151" "1" "70" "7" "141672604" "141672604" "subst" "0.485108" "00006" "TAS2R38_000003" "g.141672604T>C" "8/142 chromosomes" "{PMID:Campbell 2012:22130969}" "" "1885G>A" "" "Germline" "" "rs10246939" "0" "" "" "g.141972804T>C" "" "likely benign (dominant)" "" "0000128152" "1" "70" "7" "141672705" "141672705" "subst" "0" "00006" "TAS2R38_000002" "g.141672705A>G" "251/542 chromosomes" "{PMID:Campbell 2012:22130969}" "" "" "variant originated ago ~0.35My\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" "" "rs1726866" "0" "" "" "g.141972905A>G" "" "likely benign (dominant)" "" ## 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 TAS2R38 ## Count = 201 "{{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}}" "0000127952" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127953" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127954" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV" "0000127955" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127956" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127957" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127958" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127959" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127960" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV" "0000127961" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV" "0000127962" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI" "0000127963" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127964" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127965" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127966" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127967" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127968" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PVI" "0000127969" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127970" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV" "0000127971" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127972" "00020774" "70" "886" "0" "886" "0" "c.886A>G" "r.(?)" "p.(Ile296Val)" "1" "AAV" "0000127973" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127974" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127975" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127976" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127977" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127978" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV" "0000127979" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H1)" "0000127980" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV (H2)" "0000127981" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H3)" "0000127982" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127983" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H1)" "0000127984" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAV (H2)" "0000127985" "00020774" "50" "809" "0" "809" "0" "c.809T>G" "r.(?)" "p.(Leu270Arg)" "1" "AVI (H7)" "0000127986" "00020774" "50" "649" "0" "649" "0" "c.649A>C" "r.(?)" "p.(Thr217Pro)" "1" "AVI (H8)" "0000127987" "00020774" "50" "403" "0" "403" "0" "c.403T>G" "r.(?)" "p.(Trp135Gly)" "1" "AAI (H9)" "0000127988" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H3)" "0000127989" "00020774" "50" "239" "0" "239" "0" "c.239A>G" "r.(?)" "p.(His80Arg)" "1" "AAI (H11)" "0000127990" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127991" "00020774" "50" "191" "0" "191" "0" "c.191G>A" "r.(?)" "p.(Arg64Gln)" "1" "AVI (H13)" "0000127992" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000127993" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H15)" "0000127994" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H16)" "0000127995" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H17)" "0000127996" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000127997" "00020774" "50" "106" "0" "106" "0" "c.106G>A" "r.(?)" "p.(Val36Ile)" "1" "PAV (H19)" "0000127998" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H20)" "0000127999" "00020774" "50" "17" "0" "17" "0" "c.17G>A" "r.(?)" "p.(Arg6His)" "1" "AVI (H21)" "0000128000" "00020774" "50" "403" "0" "403" "0" "c.403T>G" "r.(?)" "p.(Trp135Gly)" "1" "AAI (H9)" "0000128001" "00020774" "50" "362" "0" "362" "0" "c.362T>C" "r.(?)" "p.(Leu121Pro)" "1" "AAI (H10)" "0000128002" "00020774" "50" "239" "0" "239" "0" "c.239A>G" "r.(?)" "p.(His80Arg)" "1" "AAI (H11)" "0000128003" "00020774" "50" "239" "0" "239" "0" "c.239A>G" "r.(?)" "p.(His80Arg)" "1" "AAI (H12)" "0000128004" "00020774" "50" "191" "0" "191" "0" "c.191G>A" "r.(?)" "p.(Arg64Gln)" "1" "AVI (H13)" "0000128005" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128006" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H15)" "0000128007" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H16)" "0000128008" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H17)" "0000128009" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H1)" "0000128010" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000128011" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128012" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000128013" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128014" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H18)" "0000128015" "00020774" "70" "785" "0" "785" "0" "c.785T>C" "r.(?)" "p.(Val262Ala)" "1" "AAI (H1)" "0000128016" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000128017" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128018" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000128019" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128020" "00020774" "50" "822" "0" "822" "0" "c.822C>T" "r.(?)" "p.(=)" "1" "AVI (H6)" "0000128021" "00020774" "10" "0" "0" "0" "0" "c.=" "r.=" "p.=" "1" "AVI" "0000128022" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H14)" "0000128023" "00020774" "70" "145" "0" "145" "0" "c.145G>C" "r.(?)" "p.(Ala49Pro)" "1" "PAV (H18)" "0000128024" "00020774" "50" "-992" "0" "-992" "0" "c.-992A>G" "r.(?)" "p.(=)" "_1" "" "0000128025" "00020774" "50" "-926" "0" "-926" "0" "c.-926A>C" "r.(?)" "p.(=)" "_1" "" "0000128026" "00020774" "50" "-924" "0" "-924" "0" "c.-924G>C" "r.(?)" 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"p.(Val262Ala)" "1" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 201 "{{screeningid}}" "{{variantid}}" "0000079313" "0000127952" "0000079314" "0000127953" "0000079314" "0000128066" "0000079314" "0000128067" "0000079315" "0000127954" "0000079315" "0000128068" "0000079316" "0000127955" "0000079316" "0000128069" "0000079316" "0000128070" "0000079317" "0000127956" "0000079318" "0000127957" "0000079319" "0000127958" "0000079320" "0000127959" "0000079321" "0000127960" "0000079321" "0000128071" "0000079322" "0000127961" "0000079322" "0000128072" "0000079323" "0000127962" "0000079324" "0000127963" "0000079324" "0000128073" "0000079324" "0000128074" "0000079325" "0000127964" "0000079325" "0000128075" "0000079325" "0000128076" "0000079326" "0000127965" "0000079326" "0000128077" "0000079326" "0000128078" "0000079327" "0000127966" "0000079327" "0000128079" "0000079327" "0000128080" "0000079328" "0000127967" "0000079328" "0000128081" "0000079328" "0000128082" 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