### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NLRP5) # 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}}" "NLRP5" "NLR family, pyrin domain containing 5" "19" "q13.43" "unknown" "NC_000019.9" "UD_134407658586" "" "https://www.LOVD.nl/NLRP5" "" "1" "21269" "126206" "609658" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "https://databases.lovd.nl/shared/refseq/NLRP5_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2024-11-10 20:56:22" "00006" "2024-12-27 11:38:38" ## 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}}" "00014624" "NLRP5" "NLR family, pyrin domain containing 5" "001" "NM_153447.4" "" "NP_703148.4" "" "" "" "1" "3885" "3603" "56511092" "56573176" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 5 "{{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" "" "" "00232" "SRS;RSS" "Silver-Russell syndrome (SRS, Russell-Silver syndrome (RSS))" "AD" "180860" "" "" "" "00006" "2013-10-09 19:30:21" "00006" "2021-12-10 21:51:32" "05370" "INFF" "infertility, female (INFF)" "" "" "" "" "" "00006" "2017-12-29 16:08:25" "" "" "07113" "OZEMA19" "oocyte/zygote/embryo maturation arrest, type 19" "AR" "620333" "" "" "" "00006" "2024-11-10 20:57:22" "" "" "07114" "MLID" "multilocus imprinting disturbances" "" "" "" "" "" "00006" "2024-11-11 09:01:04" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 2 "{{geneid}}" "{{diseaseid}}" "NLRP5" "05370" "NLRP5" "07113" ## Individuals ## Do not remove or alter this header ## ## Count = 28 "{{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}}" "00164469" "" "" "" "1" "" "00663" "" "" "" "" "" "" "0" "" "" "" "" "00165246" "" "" "" "1" "" "00663" "" "" "F" "?" "Germany" "" "0" "" "" "" "SRS-38M" "00457392" "" "" "" "2" "" "00006" "{PMID:Mu 2019:30877238}" "2-generation family, 2 affected sisters, unaffected parents" "F" "" "China" "" "0" "" "" "" "Fam6PatII1" "00457393" "" "" "00457392" "1" "" "00006" "{PMID:Mu 2019:30877238}" "sister" "F" "" "China" "" "0" "" "" "" "Fam6PatII2" "00457394" "" "" "" "1" "" "00006" "{PMID:Mu 2019:30877238}" "3-generation family, 1 affected, unaffected parents" "F" "" "China" "" "0" "" "" "" "FamPat7" "00457395" "" "" "" "3" "" "00006" "{PMID:Docherty 2015:26323243}" "mother of 2 affected children (F, M), 6 pregnancy losses and one termination (presumed molar pregnancy), with three unrelated partners; no methylation disturbances" "F" "" "" "" "0" "" "" "" "Fam1" "00457396" "" "" "" "3" "" "00006" "{PMID:Docherty 2015:26323243}" "mother of 2 affected children (2M), 4 pregnancy losses; no methylation disturbances" "F" "" "" "" "0" "" "" "" "Fam2" "00457397" "" "" "" "2" "" "00006" "{PMID:Docherty 2015:26323243}" "mother of affected child; no methylation disturbances" "F" "" "" "" "0" "" "" "" "Fam3" "00457398" "" "" "" "2" "" "00006" "{PMID:Docherty 2015:26323243}" "mother of affected child; no methylation disturbances" "F" "" "Germany" "" "0" "" "" "" "Fam4" "00457399" "" "" "" "2" "" "00006" "{PMID:Docherty 2015:26323243}" "mother of affected child; no methylation disturbances" "F" "" "" "" "0" "" "" "" "Fam5" "00457400" "" "" "00457395" "1" "" "00006" "{PMID:Docherty 2015:26323243}" "daughter" "F" "" "" "" "0" "" "" "" "Fam1PatII2" "00457401" "" "" "00457396" "1" "" "00006" "{PMID:Docherty 2015:26323243}" "son" "M" "" "" "" "0" "" "" "" "Fam2PatII4" "00457402" "" "" "00457397" "1" "" "00006" "{PMID:Docherty 2015:26323243}" "son" "M" "" "" "" "0" "" "" "" "Fam3PatII2" "00457404" "" "" "00457399" "1" "" "00006" "{PMID:Balpe 2011:21206512}, {PMID:Docherty 2015:26323243}" "daughter" "F" "" "" "" "0" "" "" "" "Fam5PatII3" "00457405" "" "" "00457396" "1" "" "00006" "{PMID:Docherty 2015:26323243}" "son" "M" "" "" "" "0" "" "" "" "Fam2PatII8" "00457406" "" "" "00457395" "1" "" "00006" "{PMID:Docherty 2015:26323243}" "son" "M" "" "" "" "0" "" "" "" "Fam1PatII8" "00457440" "" "" "" "1" "" "00006" "{PMID:Huang 2022:35091966}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "yes" "China" "" "0" "" "" "" "Pat1" "00457443" "" "" "" "1" "" "00006" "{PMID:Tong 2022:35946397}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "" "China" "" "0" "" "" "" "Fam2" "00457444" "" "" "" "1" "" "00006" "{PMID:Tong 2022:35946397}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "" "China" "" "0" "" "" "" "Fam3" "00457445" "" "" "" "2" "" "00006" "{PMID:Tong 2022:35946397}" "2-generation family, 2 affected sisters, unaffected heterozygous carrier parents" "F" "" "China" "" "0" "" "" "" "Fam4Pat4" "00457446" "" "" "" "1" "" "00006" "{PMID:Tong 2022:35946397}" "sister" "F" "" "China" "" "0" "" "" "" "Fam4Pat5" "00458496" "" "" "" "1" "" "04780" "" "" "F" "" "" "" "" "" "" "" "" "00458497" "" "" "" "1" "" "04780" "" "" "F" "" "" "" "" "" "" "" "" "00458498" "" "" "" "1" "" "04780" "" "" "" "" "" "" "" "" "" "" "" "00458499" "" "" "" "1" "" "04780" "" "" "" "" "" "" "" "" "" "" "" "00458500" "" "" "" "1" "" "04780" "" "" "" "" "" "" "" "" "" "" "" "00458501" "" "" "" "1" "" "04780" "" "" "" "" "" "" "" "" "" "" "" "00458502" "" "" "" "1" "" "04780" "" "" "" "" "" "" "" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 27 "{{individualid}}" "{{diseaseid}}" "00165246" "00232" "00457392" "05370" "00457393" "05370" "00457394" "05370" "00457395" "00000" "00457396" "00000" "00457397" "00000" "00457398" "00000" "00457399" "00000" "00457400" "07114" "00457401" "07114" "00457402" "07114" "00457404" "07114" "00457405" "07114" "00457406" "07114" "00457440" "05370" "00457443" "05370" "00457444" "05370" "00457445" "05370" "00457446" "05370" "00458496" "07113" "00458497" "07113" "00458498" "07113" "00458499" "07113" "00458500" "07113" "00458501" "07113" "00458502" "07113" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00000, 00232, 05370, 07113, 07114 ## Count = 27 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Head/Microcephaly}}" "{{Phenotype/Birth/Gestational_age_wk}}" "{{Phenotype/Feeding/Problems}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Intrauterine_growth_retardation/HPO/0001511}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Growth/Retardation/Postnatal/HPO_0008897}}" "{{Phenotype/Asymmetry/Body}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000130125" "00232" "00165246" "00663" "Unknown" "" "" "" "no macrocephaly" "" "" "" "" "" "normal" "" "" "" "normal" "" "ascertained as mother of SRS with multilocus defect" "" "0000345856" "05370" "00457392" "00006" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "primary infertility" "0000345857" "05370" "00457393" "00006" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "primary infertility" "0000345858" "05370" "00457394" "00006" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "primary infertility" "0000345859" "00000" "00457395" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "carrier multilocus imprinting disturbances" "0000345860" "00000" "00457396" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "carrier multilocus imprinting disturbances" "0000345861" "00000" "00457397" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "carrier multilocus imprinting disturbances" "0000345862" "00000" "00457398" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "carrier multilocus imprinting disturbances" "0000345863" "00000" "00457399" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "carrier multilocus imprinting disturbances" "0000345864" "07114" "00457400" "00006" "Unknown" "" "see paper; ..., Silver Russel syndrome (multilocus imprinting disturbances); birth 32w;" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "atypical Silver Russell syndrome" "0000345865" "07114" "00457401" "00006" "Unknown" "" "see paper; ..., Beckwith Wiedemann syndrome (multilocus imprinting disturbances)" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "Beckwith Wiedemann syndrome" "0000345866" "07114" "00457402" "00006" "Unknown" "" "see paper; ..., Beckwith Wiedemann syndrome (multilocus imprinting disturbances)" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "non-specific autism and obesity" "0000345868" "07114" "00457404" "00006" "Unknown" "" "see paper; ..., non-specific growth, developmental delay and unusual behaviour (multilocus imprinting disturbances)" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "multilocus imprinting disturbances" "0000345869" "07114" "00457405" "00006" "Unknown" "" "see paper; ..., non-specific developmental and marked behavioural problems (autism, extreme separation anxiety), obesity (multilocus imprinting disturbances)" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "multilocus imprinting disturbances" "0000345870" "07114" "00457406" "00006" "Unknown" "" "see paper; ..., Beckwith Wiedemann syndrome (multilocus imprinting disturbances)" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "Beckwith Wiedemann syndrome" "0000345904" "05370" "00457440" "00006" "Familial, autosomal recessive" "34y" "see paper; ..., oocyte maturation arrest at the germinal vesicle stage" "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "female infertility" "0000345907" "05370" "00457443" "00006" "Familial, autosomal recessive" "23y" "see paper; ..., recurrent preimplantation embryonic arrest during assisted reproductive technology treatment" "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "female infertility" "0000345908" "05370" "00457444" "00006" "Familial, autosomal recessive" "31y" "see paper; ..., recurrent preimplantation embryonic arrest during assisted reproductive technology treatment" "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "female infertility" "0000345909" "05370" "00457445" "00006" "Familial, autosomal recessive" "38y" "see paper; ..., recurrent preimplantation embryonic arrest during assisted reproductive technology treatment" "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "female infertility" "0000345910" "05370" "00457446" "00006" "Familial, autosomal recessive" "43y" "see paper; ..., 33y-history of spontaneous\r\nabortion; 43y-preimplantation embryonic arrest during assisted reproductive technology treatment" "" "" "" "" "" "" "" "" "" "" "" "" "" "OZEMA19" "female infertility" "0000346933" "07113" "00458496" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346934" "07113" "00458497" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346935" "07113" "00458498" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346936" "07113" "00458499" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346937" "07113" "00458500" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346938" "07113" "00458501" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000346939" "07113" "00458502" "04780" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 28 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000165337" "00164469" "1" "00663" "" "2018-05-23 15:21:13" "00006" "2018-06-01 14:51:27" "SEQ-NG-I" "DNA" "lymphocytes" "" "0000166124" "00165246" "1" "00663" "00663" "2018-07-04 08:17:36" "" "" "SEQ-NG-I" "DNA" "lymphocytes" "" "0000459013" "00457392" "1" "00006" "00006" "2024-11-10 21:23:50" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459014" "00457393" "1" "00006" "00006" "2024-11-10 21:23:50" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459015" "00457394" "1" "00006" "00006" "2024-11-10 21:23:50" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459016" "00457395" "1" "00006" "00006" "2024-11-11 09:07:54" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459017" "00457396" "1" "00006" "00006" "2024-11-11 09:07:54" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459018" "00457397" "1" "00006" "00006" "2024-11-11 09:07:54" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459019" "00457398" "1" "00006" "00006" "2024-11-11 09:07:54" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459020" "00457399" "1" "00006" "00006" "2024-11-11 09:07:54" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459021" "00457400" "1" "00006" "00006" "2024-11-11 09:31:20" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459022" "00457401" "1" "00006" "00006" "2024-11-11 09:31:20" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459023" "00457402" "1" "00006" "00006" "2024-11-11 09:31:20" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459025" "00457404" "1" "00006" "00006" "2024-11-11 09:31:20" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459026" "00457405" "1" "00006" "00006" "2024-11-11 09:31:20" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459027" "00457406" "1" "00006" "00006" "2024-11-11 09:48:36" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459061" "00457440" "1" "00006" "00006" "2024-11-11 16:21:02" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459064" "00457443" "1" "00006" "00006" "2024-11-11 18:05:07" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459065" "00457444" "1" "00006" "00006" "2024-11-11 18:05:07" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459066" "00457445" "1" "00006" "00006" "2024-11-11 18:05:07" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000459067" "00457446" "1" "00006" "00006" "2024-11-11 18:05:07" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000460118" "00458496" "1" "04780" "04780" "2024-12-15 09:41:52" "" "" "SEQ-NG-I" "DNA" "" "" "0000460119" "00458497" "1" "04780" "04780" "2024-12-15 10:01:02" "" "" "SEQ-NG-I" "DNA" "" "" "0000460120" "00458498" "1" "04780" "04780" "2024-12-15 10:09:44" "" "" "SEQ-NG-I" "DNA" "" "" "0000460121" "00458499" "1" "04780" "04780" "2024-12-15 10:15:06" "" "" "SEQ-NG-I" "DNA" "" "" "0000460122" "00458500" "1" "04780" "04780" "2024-12-15 10:26:14" "" "" "SEQ-NG-I" "DNA" "" "" "0000460123" "00458501" "1" "04780" "04780" "2024-12-15 10:31:14" "" "" "SEQ-NG-I" "DNA" "" "" "0000460124" "00458502" "1" "04780" "04780" "2024-12-15 10:35:40" "" "" "SEQ-NG-I" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 9 "{{screeningid}}" "{{geneid}}" "0000165337" "NLRP5" "0000166124" "NLRP5" "0000460118" "NLRP5" "0000460119" "NLRP5" "0000460120" "NLRP5" "0000460121" "NLRP5" "0000460122" "NLRP5" "0000460123" "NLRP5" "0000460124" "NLRP5" ## 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 = 52 "{{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}}" "0000369000" "0" "50" "19" "56515087" "56515087" "subst" "8.71323E-6" "00663" "NLRP5_000001" "g.56515087T>A" "" "" "" "" "" "Germline" "" "rs753824534" "0" "" "" "g.56003721T>A" "" "VUS" "" "0000370556" "0" "50" "19" "56565134" "56565134" "subst" "8.13094E-6" "00663" "NLRP5_000002" "g.56565134G>A" "" "" "" "" "" "Germline" "" "rs762535392" "0" "altered methylation in the child" "" "g.56053768G>A" "" "VUS" "" "0000568559" "0" "30" "19" "56515426" "56515426" "subst" "0.00127292" "01804" "NLRP5_000003" "g.56515426G>A" "" "" "" "NLRP5(NM_153447.4):c.407G>A (p.(Arg136Gln))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56004060G>A" "" "likely benign" "" "0000568561" "0" "30" "19" "56544146" "56544146" "subst" "0" "01804" "NLRP5_000005" "g.56544146A>T" "" "" "" "NLRP5(NM_153447.4):c.2446A>T (p.(Met816Leu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56032780A>T" "" "likely benign" "" "0000568562" "0" "30" "19" "56545029" "56545029" "subst" "0" "01804" "NLRP5_000006" "g.56545029G>A" "" "" "" "NLRP5(NM_153447.4):c.2569G>A (p.(Ala857Thr))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56033663G>A" "" "likely benign" "" "0000568563" "0" "30" "19" "56552326" "56552326" "subst" "4.06511E-6" "01804" "NLRP5_000007" "g.56552326G>A" "" "" "" "NLRP5(NM_153447.4):c.2825G>A (p.(Ser942Asn))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56040960G>A" "" "likely benign" "" "0000617892" "0" "50" "19" "56538665" "56538665" "subst" "0.000814312" "01943" "NLRP5_000008" "g.56538665A>G" "" "" "" "NLRP5(NM_153447.4):c.1066A>G (p.R356G)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56027299A>G" "" "VUS" "" "0000617893" "0" "30" "19" "56539327" "56539327" "subst" "7.31297E-5" "01943" "NLRP5_000009" "g.56539327T>C" "" "" "" "NLRP5(NM_153447.4):c.1728T>C (p.C576=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.56027961T>C" "" "likely benign" "" "0000809067" "0" "30" "19" "56544050" "56544050" "subst" "0" "01943" "NLRP5_000011" "g.56544050C>A" "" "" "" "NLRP5(NM_153447.4):c.2350C>A (p.R784=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001005164" "0" "30" "19" "56539284" "56539284" "subst" "0.00491102" "01804" "NLRP5_000012" "g.56539284G>A" "" "" "" "NLRP5(NM_153447.4):c.1685G>A (p.(Arg562His))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001016711" "1" "90" "19" "56515311" "56515311" "subst" "0" "00006" "NLRP5_000013" "g.56515311C>T" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "yes" "" "0" "" "" "g.56003945C>T" "" "pathogenic (recessive)" "" "0001016712" "1" "90" "19" "56515311" "56515311" "subst" "0" "00006" "NLRP5_000013" "g.56515311C>T" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "yes" "" "0" "" "" "g.56003945C>T" "" "pathogenic (recessive)" "" "0001016713" "21" "90" "19" "56538465" "56538465" "subst" "0" "00006" "NLRP5_000014" "g.56538465G>A" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "" "" "0" "" "" "g.56027099G>A" "" "pathogenic (recessive)" "" "0001016718" "2" "90" "19" "56539680" "56539680" "subst" "0" "00006" "NLRP5_000015" "g.56539680C>T" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "yes" "" "0" "" "" "g.56028314C>T" "" "pathogenic (recessive)" "" "0001016719" "2" "90" "19" "56539680" "56539680" "subst" "0" "00006" "NLRP5_000015" "g.56539680C>T" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "yes" "" "0" "" "" "g.56028314C>T" "" "pathogenic (recessive)" "" "0001016720" "11" "90" "19" "56569626" "56569626" "subst" "0" "00006" "NLRP5_000016" "g.56569626C>T" "" "{PMID:Mu 2019:30877238}" "" "" "" "Germline" "" "" "0" "" "" "g.56058260C>T" "" "pathogenic (recessive)" "" "0001016721" "1" "95" "19" "56539263" "56539263" "subst" "0" "00006" "NLRP5_000017" "g.56539263G>T" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "" "0" "" "" "g.56027897G>T" "" "pathogenic (!)" "" "0001016722" "21" "95" "19" "56544020" "56544020" "subst" "4.06507E-6" "00006" "NLRP5_000018" "g.56544020T>C" "rs370837790" "{PMID:Docherty 2015:263232432}" "" "" "variant affects embryonic imprinting" "Germline" "" "" "0" "multilocus imprinting disturbances" "" "g.56032654T>C" "" "pathogenic (!)" "" "0001016723" "2" "95" "19" "56544020" "56544020" "subst" "4.06507E-6" "00006" "NLRP5_000018" "g.56544020T>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "rs370837790" "0" "" "" "g.56032654T>C" "" "pathogenic (!)" "" "0001016724" "21" "95" "19" "56539263" "56539263" "subst" "0" "00006" "NLRP5_000017" "g.56539263G>T" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "" "0" "multilocus imprinting disturbances" "" "g.56027897G>T" "" "pathogenic (!)" "" "0001016725" "11" "95" "19" "56544053" "56544053" "subst" "7.72245E-5" "00006" "NLRP5_000019" "g.56544053C>T" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "rs200446614" "0" "" "" "g.56032687C>T" "" "pathogenic (!)" "" "0001016726" "21" "95" "19" "56552341" "56552341" "subst" "0.000251928" "00006" "NLRP5_000020" "g.56552341T>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "rs202181446" "0" "" "" "g.56040975T>C" "" "pathogenic (!)" "" "0001016727" "21" "95" "19" "56544053" "56544053" "subst" "7.72245E-5" "00006" "NLRP5_000019" "g.56544053C>T" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "rs200446614" "0" "multilocus imprinting disturbances" "" "g.56032687C>T" "" "pathogenic (!)" "" "0001016728" "21" "95" "19" "56544053" "56544053" "subst" "7.72245E-5" "00006" "NLRP5_000019" "g.56544053C>T" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "rs200446614" "0" "multilocus imprinting disturbances" "" "g.56032687C>T" "" "pathogenic (!)" "" "0001016729" "21" "90" "19" "56515174" "56515174" "subst" "8.12262E-6" "00006" "NLRP5_000021" "g.56515174T>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "" "0" "multilocus imprinting disturbances" "" "g.56003808T>C" "" "pathogenic (!)" "" "0001016730" "21" "95" "19" "56515245" "56515245" "subst" "8.12269E-6" "00006" "NLRP5_000022" "g.56515245G>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline" "" "" "0" "multilocus imprinting disturbances" "" "g.56003879G>C" "" "pathogenic (!)" "" "0001016731" "1" "95" "19" "56515245" "56515245" "subst" "8.12269E-6" "00006" "NLRP5_000022" "g.56515245G>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "" "0" "" "" "g.56003879G>C" "" "pathogenic (!)" "" "0001016732" "1" "95" "19" "56515174" "56515174" "subst" "8.12262E-6" "00006" "NLRP5_000021" "g.56515174T>C" "" "{PMID:Docherty 2015:26323243}" "" "" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "" "0" "" "" "g.56003808T>C" "" "pathogenic (!)" "" "0001016733" "0" "95" "19" "56538755" "56538757" "dup" "0" "00006" "NLRP5_000023" "g.56538755_56538757dup" "" "{PMID:Docherty 2015:26323243}" "" "1156_1158dupCCT" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "" "0" "" "" "g.56027391_56027393dup" "" "pathogenic (!)" "" "0001016734" "3" "95" "19" "56539298" "56539298" "subst" "4.47136E-5" "00006" "NLRP5_000024" "g.56539298A>G" "" "see paper; ..., Silver Russel syndrome (multilocus imprinting disturbances)" "" "" "variant affects embryonic imprinting" "Germline/De novo (untested)" "" "" "0" "" "" "g.56027932A>G" "" "pathogenic (!)" "" "0001016735" "21" "95" "19" "56539298" "56539298" "subst" "4.47136E-5" "00006" "NLRP5_000024" "g.56539298A>G" "" "see paper; ..., Silver Russel syndrome (multilocus imprinting disturbances)" "" "" "variant affects embryonic imprinting" "Germline" "" "" "0" "multilocus imprinting disturbances" "" "g.56027932A>G" "" "pathogenic (!)" "" "0001016778" "3" "90" "19" "56538885" "56538888" "del" "0" "00006" "NLRP5_000025" "g.56538885_56538888del" "" "{PMID:Huang 2022:35091966}" "" "" "" "Germline" "" "" "0" "" "" "g.56027519_56027522del" "" "pathogenic (recessive)" "" "0001016782" "11" "90" "19" "56538570" "56538570" "subst" "0" "00006" "NLRP5_000026" "g.56538570T>A" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "" "" "0" "" "" "g.56027204T>A" "" "pathogenic (recessive)" "" "0001016783" "21" "90" "19" "56569647" "56569647" "subst" "0" "00006" "NLRP5_000027" "g.56569647T>C" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "" "" "0" "" "" "g.56058281T>C" "" "pathogenic (recessive)" "" "0001016784" "11" "90" "19" "56539429" "56539430" "del" "0" "00006" "NLRP5_000028" "g.56539429_56539430del" "" "{PMID:Tong 2022:35946397}" "" "1830_1831delGT" "" "Germline" "" "" "0" "" "" "g.56028063_56028064del" "" "pathogenic (recessive)" "" "0001016785" "21" "90" "19" "56539174" "56539175" "del" "0" "00006" "NLRP5_000029" "g.56539174_56539175del" "" "{PMID:Tong 2022:35946397}" "" "1575_1576delAG" "" "Germline" "" "" "0" "" "" "g.56027808_56027809del" "" "pathogenic (recessive)" "" "0001016786" "11" "90" "19" "56538801" "56538801" "subst" "0" "00006" "NLRP5_000030" "g.56538801C>T" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "yes" "" "0" "" "" "g.56027435C>T" "" "pathogenic (recessive)" "" "0001016787" "21" "90" "19" "56544078" "56544078" "subst" "0" "00006" "NLRP5_000031" "g.56544078T>G" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "" "" "0" "" "" "g.56032712T>G" "" "pathogenic (recessive)" "" "0001016788" "11" "90" "19" "56538801" "56538801" "subst" "0" "00006" "NLRP5_000030" "g.56538801C>T" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "" "" "0" "" "" "g.56027435C>T" "" "pathogenic (recessive)" "" "0001016789" "21" "90" "19" "56544078" "56544078" "subst" "0" "00006" "NLRP5_000031" "g.56544078T>G" "" "{PMID:Tong 2022:35946397}" "" "" "" "Germline" "" "" "0" "" "" "g.56032712T>G" "" "pathogenic (recessive)" "" "0001019075" "21" "70" "19" "56515237" "56515257" "dup" "0" "04780" "NLRP5_000032" "g.56515237_56515257dup" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56003871_56003891dup" "" "VUS" "ACMG" "0001019076" "11" "70" "19" "56539808" "56539808" "subst" "2.0403E-5" "04780" "NLRP5_000039" "g.56539808C>T" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56028442C>T" "" "VUS" "" "0001019077" "3" "70" "19" "56539367" "56539367" "subst" "0" "04780" "NLRP5_000037" "g.56539367T>C" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56028001T>C" "" "VUS" "" "0001019078" "0" "70" "19" "56538997" "56538997" "subst" "0" "04780" "NLRP5_000036" "g.56538997C>A" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56027631C>A" "" "VUS" "" "0001019079" "0" "70" "19" "56544051" "56544051" "subst" "4.87745E-5" "04780" "NLRP5_000040" "g.56544051G>A" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56032685G>A" "" "VUS" "" "0001019080" "21" "70" "19" "56538660" "56538660" "subst" "1.22869E-5" "04780" "NLRP5_000034" "g.56538660C>T" "" "" "" "" "no variant 2nd chromosome reported" "Germline" "" "" "0" "" "" "g.56027294C>T" "" "likely pathogenic (recessive)" "" "0001019081" "0" "70" "19" "56538477" "56538477" "subst" "0" "04780" "NLRP5_000033" "g.56538477C>T" "" "" "" "" "" "De novo" "" "" "0" "" "" "g.56027111C>T" "" "VUS" "ACMG" "0001019082" "21" "90" "19" "56539174" "56539175" "del" "0" "04780" "NLRP5_000029" "g.56539174_56539175del" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56027808_56027809del" "" "likely pathogenic" "ACMG" "0001019083" "0" "70" "19" "56538791" "56538791" "subst" "4.0812E-5" "04780" "NLRP5_000035" "g.56538791G>A" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.56027425G>A" "" "VUS" "ACMG" "0001019084" "0" "70" "19" "56544051" "56544051" "subst" "4.87745E-5" "04780" "NLRP5_000040" "g.56544051G>A" "" "" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.56032685G>A" "" "VUS" "ACMG" "0001019085" "0" "70" "19" "56538885" "56538888" "del" "0" "04780" "NLRP5_000025" "g.56538885_56538888del" "" "" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.56027519_56027522del" "" "likely pathogenic (recessive)" "ACMG" "0001019086" "0" "70" "19" "56539676" "56539676" "subst" "2.03062E-5" "04780" "NLRP5_000038" "g.56539676G>A" "" "" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.56028310G>A" "" "VUS" "ACMG" ## 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 NLRP5 ## Count = 52 "{{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}}" "0000369000" "00014624" "50" "68" "0" "68" "0" "c.68T>A" "r.(?)" "p.(Val23Asp)" "2" "0000370556" "00014624" "50" "3259" "0" "3259" "0" "c.3259G>A" "r.(?)" "p.(Glu1087Lys)" "" "0000568559" "00014624" "30" "407" "0" "407" "0" "c.407G>A" "r.(?)" "p.(Arg136Gln)" "" "0000568561" "00014624" "30" "2446" "0" "2446" "0" "c.2446A>T" "r.(?)" "p.(Met816Leu)" "" "0000568562" "00014624" "30" "2569" "0" "2569" "0" "c.2569G>A" "r.(?)" "p.(Ala857Thr)" "" "0000568563" "00014624" "30" "2825" "0" "2825" "0" "c.2825G>A" "r.(?)" "p.(Ser942Asn)" "" "0000617892" "00014624" "50" "1066" "0" "1066" "0" "c.1066A>G" "r.(?)" "p.(Arg356Gly)" "" "0000617893" "00014624" "30" "1728" "0" "1728" "0" "c.1728T>C" "r.(?)" "p.(Cys576=)" "" "0000809067" "00014624" "30" "2350" "0" "2350" "0" "c.2350C>A" "r.(?)" "p.(Arg784=)" "" "0001005164" "00014624" "30" "1685" "0" "1685" "0" "c.1685G>A" "r.(?)" "p.(Arg562His)" "" "0001016711" "00014624" "90" "292" "0" "292" "0" "c.292C>T" "r.(?)" "p.(Gln98Ter)" "" "0001016712" "00014624" "90" "292" "0" "292" "0" "c.292C>T" "r.(?)" "p.(Gln98Ter)" "" "0001016713" "00014624" "90" "866" "0" "866" "0" "c.866G>A" "r.(?)" "p.(Gly289Glu)" "" "0001016718" "00014624" "90" "2081" "0" "2081" "0" "c.2081C>T" "r.(?)" "p.(Thr694Ile)" "" "0001016719" "00014624" "90" "2081" "0" "2081" "0" "c.2081C>T" "r.(?)" "p.(Thr694Ile)" "" "0001016720" "00014624" "90" "3320" "0" "3320" "0" "c.3320C>T" "r.(?)" "p.(Thr1107Ile)" "" "0001016721" "00014624" "95" "1664" "0" "1664" "0" "c.1664G>T" "r.(?)" "p.(Gly555Val)" "" "0001016722" "00014624" "95" "2320" "0" "2320" "0" "c.2320T>C" "r.(?)" "p.(Cys774Arg)" "" "0001016723" "00014624" "95" "2320" "0" "2320" "0" "c.2320T>C" "r.(?)" "p.(Cys774Arg)" "" "0001016724" "00014624" "95" "1664" "0" "1664" "0" "c.1664G>T" "r.(?)" "p.(Gly555Val)" "" "0001016725" "00014624" "95" "2353" "0" "2353" "0" "c.2353C>T" "r.(?)" "p.(Gln785*)" "" "0001016726" "00014624" "95" "2840" "0" "2840" "0" "c.2840T>C" "r.(?)" "p.(Leu947Pro)" "" "0001016727" "00014624" "95" "2353" "0" "2353" "0" "c.2353C>T" "r.(?)" "p.(Gln785*)" "" "0001016728" "00014624" "95" "2353" "0" "2353" "0" "c.2353C>T" "r.(?)" "p.(Gln785*)" "" "0001016729" "00014624" "90" "155" "0" "155" "0" "c.155T>C" "r.(?)" "p.(Met52Thr)" "" "0001016730" "00014624" "95" "226" "0" "226" "0" "c.226G>C" "r.(?)" "p.(Glu76Gln)" "" "0001016731" "00014624" "95" "226" "0" "226" "0" "c.226G>C" "r.(?)" "p.(Glu76Gln)" "" "0001016732" "00014624" "95" "155" "0" "155" "0" "c.155T>C" "r.(?)" "p.(Met52Thr)" "" "0001016733" "00014624" "95" "1158" "0" "1160" "0" "c.1158_1160dup" "r.(?)" "p.(Pro387dup)" "" "0001016734" "00014624" "95" "1699" "0" "1699" "0" "c.1699A>G" "r.(?)" "p.(Met567Val)" "" "0001016735" "00014624" "95" "1699" "0" "1699" "0" "c.1699A>G" "r.(?)" "p.(Met567Val)" "" "0001016778" "00014624" "90" "1286" "0" "1289" "0" "c.1286_1289del" "r.(?)" "p.(Val429Glufs*30)" "" "0001016782" "00014624" "90" "971" "0" "971" "0" "c.971T>A" "r.(?)" "p.(Met324Lys)" "" "0001016783" "00014624" "90" "3341" "0" "3341" "0" "c.3341T>C" "r.(?)" "p.(Leu1114Pro)" "" "0001016784" "00014624" "90" "1830" "0" "1831" "0" "c.1830_1831del" "r.(?)" "p.(Tyr611Argfs*2)" "" "0001016785" "00014624" "90" "1575" "0" "1576" "0" "c.1575_1576del" "r.(?)" "p.(Arg525Serfs*17)" "" "0001016786" "00014624" "90" "1202" "0" "1202" "0" "c.1202C>T" "r.(?)" "p.(Pro401Leu)" "" "0001016787" "00014624" "90" "2378" "0" "2378" "0" "c.2378T>G" "r.(?)" "p.(Leu793Arg)" "" "0001016788" "00014624" "90" "1202" "0" "1202" "0" "c.1202C>T" "r.(?)" "p.(Pro401Leu)" "" "0001016789" "00014624" "90" "2378" "0" "2378" "0" "c.2378T>G" "r.(?)" "p.(Leu793Arg)" "" "0001019075" "00014624" "70" "218" "0" "238" "0" "c.218_238dup" "r.(?)" "p.(Thr79_Phe80insTyrLysGluGluPheGlnThr)" "" "0001019076" "00014624" "70" "2209" "0" "2209" "0" "c.2209C>T" "r.(?)" "p.(Arg737Trp)" "" "0001019077" "00014624" "70" "1768" "0" "1768" "0" "c.1768T>C" "r.(?)" "p.(Phe590Leu)" "" "0001019078" "00014624" "70" "1398" "0" "1398" "0" "c.1398C>A" "r.(?)" "p.(Asp466Glu)" "" "0001019079" "00014624" "70" "2351" "0" "2351" "0" "c.2351G>A" "r.(?)" "p.(Arg784Gln)" "" "0001019080" "00014624" "70" "1061" "0" "1061" "0" "c.1061C>T" "r.(?)" "p.(Pro354Leu)" "" "0001019081" "00014624" "70" "878" "0" "878" "0" "c.878C>T" "r.(?)" "p.(Ser293Leu)" "" "0001019082" "00014624" "90" "1575" "0" "1576" "0" "c.1575_1576del" "r.(?)" "p.(Arg525Serfs*17)" "" "0001019083" "00014624" "70" "1192" "0" "1192" "0" "c.1192G>A" "r.(?)" "p.(Val398Ile)" "" "0001019084" "00014624" "70" "2351" "0" "2351" "0" "c.2351G>A" "r.(?)" "p.(Arg784Gln)" "" "0001019085" "00014624" "70" "1286" "0" "1289" "0" "c.1286_1289del" "r.(?)" "p.(Val429Glufs*30)" "" "0001019086" "00014624" "70" "2077" "0" "2077" "0" "c.2077G>A" "r.(?)" "p.(Glu693Lys)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 44 "{{screeningid}}" "{{variantid}}" "0000165337" "0000369000" "0000166124" "0000370556" "0000459013" "0001016711" "0000459013" "0001016718" "0000459014" "0001016712" "0000459014" "0001016719" "0000459015" "0001016713" "0000459015" "0001016720" "0000459016" "0001016721" "0000459016" "0001016723" "0000459017" "0001016725" "0000459017" "0001016726" "0000459018" "0001016731" "0000459018" "0001016732" "0000459019" "0001016733" "0000459020" "0001016734" "0000459021" "0001016722" "0000459022" "0001016727" "0000459023" "0001016729" "0000459023" "0001016730" "0000459025" "0001016735" "0000459026" "0001016728" "0000459027" "0001016724" "0000459061" "0001016778" "0000459064" "0001016782" "0000459064" "0001016783" "0000459065" "0001016784" "0000459065" "0001016785" "0000459066" "0001016786" "0000459066" "0001016787" "0000459067" "0001016788" "0000459067" "0001016789" "0000460118" "0001019075" "0000460118" "0001019076" "0000460119" "0001019077" "0000460120" "0001019078" "0000460120" "0001019079" "0000460121" "0001019080" "0000460122" "0001019081" "0000460122" "0001019082" "0000460123" "0001019083" "0000460123" "0001019084" "0000460124" "0001019085" "0000460124" "0001019086"