{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:10597,10,HGNC:10597,94,0]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:10597","source":"HGNC:10597|sodium voltage-gated channel alpha subunit 9","targets":["1000913|NM_001365536.1(SCN9A):c.3341A>T (p.Tyr1114Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1003274|NM_001365536.1(SCN9A):c.4575C>G (p.Ile1525Met)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1003757|NM_001365536.1(SCN9A):c.794A>G (p.Gln265Arg)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1006258|NM_001365536.1(SCN9A):c.482G>C (p.Gly161Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1006744|NM_001365536.1(SCN9A):c.1583G>A (p.Arg528Lys)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1009477|NM_001365536.1(SCN9A):c.715A>G (p.Ile239Val)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1010612|NM_001365536.1(SCN9A):c.2009G>A (p.Cys670Tyr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1011667|NM_001365536.1(SCN9A):c.5921C>T (p.Thr1974Ile)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1012082|NM_001365536.1(SCN9A):c.5504G>A (p.Arg1835Gln)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1014955|NM_001365536.1(SCN9A):c.5141A>C (p.Asp1714Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1016307|NM_001365536.1(SCN9A):c.3289G>T (p.Asp1097Tyr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1016530|NM_001365536.1(SCN9A):c.3247C>T (p.Pro1083Ser)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1016793|NM_001365536.1(SCN9A):c.1324G>A (p.Ala442Thr)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1017461|NM_001365536.1(SCN9A):c.5556G>T (p.Glu1852Asp)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1017889|NM_001365536.1(SCN9A):c.2330C>T (p.Ala777Val)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1018448|NM_001365536.1(SCN9A):c.4228A>T (p.Ile1410Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1018459|NM_001365536.1(SCN9A):c.121G>A (p.Asp41Asn)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1019116|NM_001365536.1(SCN9A):c.2258G>T (p.Cys753Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1019446|NM_001365536.1(SCN9A):c.331C>G (p.Pro111Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1022096|NM_001365536.1(SCN9A):c.467+6T>C|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1022255|NM_001365536.1(SCN9A):c.4636G>A (p.Val1546Ile)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1025826|NM_001365536.1(SCN9A):c.3871A>G (p.Thr1291Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1026160|NM_001365536.1(SCN9A):c.62C>T (p.Ala21Val)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1026542|NM_001365536.1(SCN9A):c.413C>T (p.Thr138Ile)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1028064|NM_001365536.1(SCN9A):c.901A>T (p.Lys301Ter)|single nucleotide variant|Likely pathogenic|SCN9A|criteria provided, multiple submitters, no conflicts|2","1030610|NM_001365536.1(SCN9A):c.1079A>G (p.Gln360Arg)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1033965|NM_001365536.1(SCN9A):c.634G>A (p.Ala212Thr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1034557|NM_001365536.1(SCN9A):c.5393A>C (p.Glu1798Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1034700|NM_001365536.1(SCN9A):c.4G>A (p.Ala2Thr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1035555|NM_001365536.1(SCN9A):c.5338G>A (p.Glu1780Lys)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1035623|NM_001365536.1(SCN9A):c.210G>A (p.Met70Ile)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1036912|NM_001365536.1(SCN9A):c.739G>A (p.Asp247Asn)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1037492|NM_001365536.1(SCN9A):c.293T>A (p.Phe98Tyr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1037535|NM_001365536.1(SCN9A):c.77G>C (p.Arg26Pro)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1040138|NM_001365536.1(SCN9A):c.1140CTT[1] (p.Phe382del)|Microsatellite|Uncertain significance|SCN9A|criteria provided, single submitter|2","1040594|NM_001365536.1(SCN9A):c.739G>C (p.Asp247His)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1041538|NM_001365536.1(SCN9A):c.2201A>G (p.Lys734Arg)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1041882|NM_001365536.1(SCN9A):c.5408_5409del (p.Leu1802_Ser1803insTer)|Microsatellite|Uncertain significance|SCN9A|criteria provided, single submitter|2","1043657|NM_001365536.1(SCN9A):c.1085A>G (p.Tyr362Cys)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1043686|NM_001365536.1(SCN9A):c.2405A>G (p.Glu802Gly)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1050918|NM_001365536.1(SCN9A):c.3305A>G (p.Asn1102Ser)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1051190|NM_001365536.1(SCN9A):c.3413_3415del (p.Gly1138del)|Deletion|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1051486|NM_001365536.1(SCN9A):c.5018A>C (p.Asp1673Ala)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1051854|NM_001365536.1(SCN9A):c.252C>A (p.Asp84Glu)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1051966|NM_001365536.1(SCN9A):c.2036T>C (p.Met679Thr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1052526|NM_001365536.1(SCN9A):c.4297A>C (p.Met1433Leu)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1054352|NM_001365536.1(SCN9A):c.772G>A (p.Val258Met)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1054889|NM_001365536.1(SCN9A):c.966-9C>G|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1054915|NM_001365536.1(SCN9A):c.5573C>T (p.Ser1858Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1056520|NM_001365536.1(SCN9A):c.300C>G (p.Phe100Leu)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1056922|NM_001365536.1(SCN9A):c.5492T>G (p.Val1831Gly)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1057246|NM_001365536.1(SCN9A):c.786T>G (p.Ile262Met)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1058014|NM_001365536.1(SCN9A):c.5404C>T (p.Leu1802Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1058809|NM_001365536.1(SCN9A):c.5671G>A (p.Val1891Met)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1059939|NM_001365536.1(SCN9A):c.4720T>G (p.Phe1574Val)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1060767|NM_001365536.1(SCN9A):c.41A>C (p.His14Pro)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1060982|NM_001365536.1(SCN9A):c.877C>A (p.Leu293Ile)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1062109|NM_001365536.1(SCN9A):c.199C>T (p.Pro67Ser)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, multiple submitters, no conflicts|2","1063125|NM_001365536.1(SCN9A):c.1415G>C (p.Ser472Thr)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1063492|NM_001365536.1(SCN9A):c.878T>A (p.Leu293Gln)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1063846|NM_001365536.1(SCN9A):c.838C>T (p.Leu280Phe)|single nucleotide variant|Uncertain significance|SCN9A|criteria provided, single submitter|2","1067284|NM_001365536.1(SCN9A):c.596+1G>T|single nucleotide variant|Likely pathogenic|SCN9A|criteria provided, single submitter|2","1074563|NC_000002.11:g.(?_167055172)_(167060984_?)del|Deletion|Pathogenic|SCN9A|criteria provided, single submitter|2","1075008|NM_001365536.1(SCN9A):c.116del (p.Lys39fs)|Deletion|Pathogenic|SCN9A|criteria provided, single submitter|2","1075155|NM_001365536.1(SCN9A):c.4855C>T (p.Arg1619Ter)|single nucleotide variant|Pathogenic/Likely pathogenic|SCN9A|criteria provided, multiple submitters, no conflicts|2","1076959|NM_001365536.1(SCN9A):c.3801+1G>A|single nucleotide variant|Pathogenic|SCN9A|criteria provided, single submitter|2","1077510|NM_001365536.1(SCN9A):c.4665A>C (p.Ile1555=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1080526|NM_001365536.1(SCN9A):c.498A>G (p.Glu166=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1083044|NM_001365536.1(SCN9A):c.966-8G>C|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1083183|NM_001365536.1(SCN9A):c.688+8G>C|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1087575|NM_001365536.1(SCN9A):c.4452A>C (p.Ala1484=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1088491|NM_001365536.1(SCN9A):c.2880A>C (p.Leu960=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1090186|NM_001365536.1(SCN9A):c.276C>T (p.Asn92=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1096725|NM_001365536.1(SCN9A):c.177G>T (p.Leu59=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1102646|NM_001365536.1(SCN9A):c.204C>T (p.Pro68=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1104865|NM_001365536.1(SCN9A):c.114A>G (p.Glu38=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1105588|NM_001365536.1(SCN9A):c.750C>A (p.Ile250=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1106843|NM_001365536.1(SCN9A):c.180C>T (p.Pro60=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1109355|NM_001365536.1(SCN9A):c.3088C>T (p.Leu1030=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1110913|NM_001365536.1(SCN9A):c.192G>A (p.Gly64=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1112176|NM_001365536.1(SCN9A):c.5724T>C (p.Asn1908=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1117707|NM_001365536.1(SCN9A):c.2391C>A (p.Ala797=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1120447|NM_001365536.1(SCN9A):c.2931A>G (p.Thr977=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1122842|NM_001365536.1(SCN9A):c.3282G>A (p.Gly1094=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1123273|NM_001365536.1(SCN9A):c.891A>G (p.Glu297=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1123276|NM_001365536.1(SCN9A):c.4947C>T (p.Leu1649=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1123512|NM_001365536.1(SCN9A):c.3327T>C (p.Asp1109=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1123734|NM_001365536.1(SCN9A):c.780A>G (p.Ala260=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1126678|NM_001365536.1(SCN9A):c.1975-9T>G|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1129038|NM_001365536.1(SCN9A):c.4207-8T>C|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1129115|NM_001365536.1(SCN9A):c.69T>C (p.Ile23=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1130637|NM_001365536.1(SCN9A):c.4644T>C (p.Tyr1548=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1131800|NM_001365536.1(SCN9A):c.4374T>C (p.Asp1458=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1135308|NM_001365536.1(SCN9A):c.1161C>T (p.Phe387=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1142612|NM_001365536.1(SCN9A):c.849T>C (p.Asn283=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1144595|NM_001365536.1(SCN9A):c.270A>G (p.Val90=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1149243|NM_001365536.1(SCN9A):c.4728A>G (p.Val1576=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1149377|NM_001365536.1(SCN9A):c.4164C>T (p.Asn1388=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2","1156031|NM_001365536.1(SCN9A):c.267A>C (p.Ile89=)|single nucleotide variant|Conflicting classifications of pathogenicity|SCN9A|criteria provided, conflicting classifications|2","1157179|NM_001365536.1(SCN9A):c.876C>T (p.Thr292=)|single nucleotide variant|Likely benign|SCN9A|criteria provided, single submitter|2"]}]}