ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign for not specified

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Total variants: 66
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HGVS dbSNP
NM_001365536.1(SCN9A):c.1107+7A>G rs199623041
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=) rs13414203
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=) rs58465962
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=) rs184773311
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=) rs13402180
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=) rs6747673
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607
NM_001365536.1(SCN9A):c.1602+15G>T rs201987507
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_001365536.1(SCN9A):c.1975-8T>A rs752961542
NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=) rs200014315
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126
NM_001365536.1(SCN9A):c.2253C>T (p.Thr751=) rs751536693
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val) rs149707354
NM_001365536.1(SCN9A):c.2409T>C (p.Tyr803=) rs142219317
NM_001365536.1(SCN9A):c.2420G>T (p.Gly807Val) rs1553488264
NM_001365536.1(SCN9A):c.2517+6C>T rs145316463
NM_001365536.1(SCN9A):c.2634C>T (p.Phe878=) rs188678956
NM_001365536.1(SCN9A):c.2712G>A (p.Thr904=) rs200494981
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=) rs199653503
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT rs1553487749
NM_001365536.1(SCN9A):c.2875-18C>T rs1553486847
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=) rs201430964
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=) rs886038521
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu) rs4369876
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203
NM_001365536.1(SCN9A):c.3036A>G (p.Lys1012=) rs200375962
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) rs111674454
NM_001365536.1(SCN9A):c.3207C>T (p.His1069=) rs200689065
NM_001365536.1(SCN9A):c.3228T>A (p.Gly1076=) rs200393050
NM_001365536.1(SCN9A):c.3351+15T>C rs763278343
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp) rs190664764
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln) rs74401238
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858
NM_001365536.1(SCN9A):c.3506A>C (p.Asn1169Thr) rs151241025
NM_001365536.1(SCN9A):c.3540C>T (p.Asn1180=) rs766241126
NM_001365536.1(SCN9A):c.3573C>T (p.His1191=) rs375710841
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=) rs77144869
NM_001365536.1(SCN9A):c.3684T>C (p.Tyr1228=) rs144941725
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327
NM_001365536.1(SCN9A):c.3801T>C (p.Asp1267=) rs202047865
NM_001365536.1(SCN9A):c.3802-13del rs747729984
NM_001365536.1(SCN9A):c.3802-4A>G rs75230218
NM_001365536.1(SCN9A):c.3802-8T>C rs76550960
NM_001365536.1(SCN9A):c.3807T>A (p.Ser1269=) rs1272510761
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748
NM_001365536.1(SCN9A):c.3834T>G (p.Leu1278=) rs1553480111
NM_001365536.1(SCN9A):c.4141C>A (p.Arg1381=) rs748159444
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064
NM_001365536.1(SCN9A):c.4356C>T (p.Phe1452=) rs201145311
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=) rs149207258
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly) rs3750904
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968
NM_001365536.1(SCN9A):c.965+13T>C rs772337722
NM_001365536.1(SCN9A):c.965+18T>C rs1553492740
NM_001365536.1(SCN9A):c.966-8G>A rs199942413
NM_001365536.1(SCN9A):c.990T>C (p.Cys330=) rs1384436013

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