ClinVar Miner

List of variants in gene SCN10A reported as likely benign by Invitae

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Total variants: 47
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HGVS dbSNP
NM_006514.3(SCN10A):c.1138G>A (p.Val380Ile) rs142276689
NM_006514.3(SCN10A):c.1141A>G (p.Ile381Val) rs150923753
NM_006514.3(SCN10A):c.1249_1251delAAG (p.Lys417del) rs758898721
NM_006514.3(SCN10A):c.1277G>A (p.Arg426Gln) rs143033805
NM_006514.3(SCN10A):c.1641C>A (p.Gly547=) rs1444054143
NM_006514.3(SCN10A):c.1713G>A (p.Pro571=) rs148905110
NM_006514.3(SCN10A):c.1908C>T (p.Thr636=) rs147235762
NM_006514.3(SCN10A):c.1914G>A (p.Leu638=) rs774983974
NM_006514.3(SCN10A):c.1959G>A (p.Lys653=) rs1217257967
NM_006514.3(SCN10A):c.2106+8C>T rs368212766
NM_006514.3(SCN10A):c.225C>T (p.Ile75=) rs771128445
NM_006514.3(SCN10A):c.2475A>C (p.Glu825Asp) rs146028829
NM_006514.3(SCN10A):c.2484C>T (p.Pro828=) rs777634572
NM_006514.3(SCN10A):c.2499C>T (p.His833=) rs995722247
NM_006514.3(SCN10A):c.2709C>T (p.Asp903=) rs368637625
NM_006514.3(SCN10A):c.308G>A (p.Arg103Gln) rs199973777
NM_006514.3(SCN10A):c.3555G>T (p.Leu1185Phe) rs201025253
NM_006514.3(SCN10A):c.3681+9C>T rs201158753
NM_006514.3(SCN10A):c.3705G>A (p.Ala1235=) rs147376215
NM_006514.3(SCN10A):c.3711T>A (p.Ile1237=) rs148339462
NM_006514.3(SCN10A):c.3759C>T (p.Arg1253=) rs749134108
NM_006514.3(SCN10A):c.3803G>A (p.Arg1268Gln) rs138832868
NM_006514.3(SCN10A):c.3859G>A (p.Val1287Ile) rs145032037
NM_006514.3(SCN10A):c.3870C>A (p.Ile1290=) rs1371664893
NM_006514.3(SCN10A):c.4063A>G (p.Met1355Val) rs375458594
NM_006514.3(SCN10A):c.4128T>C (p.Ala1376=) rs1060504317
NM_006514.3(SCN10A):c.4137C>A (p.Ser1379=) rs779905648
NM_006514.3(SCN10A):c.4173C>T (p.Asn1391=) rs374352107
NM_006514.3(SCN10A):c.41G>T (p.Arg14Leu) rs141207048
NM_006514.3(SCN10A):c.4378C>T (p.Arg1460Trp) rs148619598
NM_006514.3(SCN10A):c.4568G>A (p.Cys1523Tyr) rs142217269
NM_006514.3(SCN10A):c.4584C>T (p.Phe1528=) rs141828577
NM_006514.3(SCN10A):c.4660C>T (p.Leu1554=) rs745999522
NM_006514.3(SCN10A):c.470+7A>G rs1173885296
NM_006514.3(SCN10A):c.4762C>A (p.Arg1588=) rs142537392
NM_006514.3(SCN10A):c.5286T>C (p.Ser1762=) rs750340252
NM_006514.3(SCN10A):c.5358C>T (p.Ile1786=) rs188413410
NM_006514.3(SCN10A):c.5451G>A (p.Glu1817=) rs1553612868
NM_006514.3(SCN10A):c.549G>A (p.Thr183=) rs141703064
NM_006514.3(SCN10A):c.5523A>G (p.Pro1841=) rs147245558
NM_006514.3(SCN10A):c.5589G>A (p.Arg1863=) rs756017969
NM_006514.3(SCN10A):c.55G>A (p.Glu19Lys) rs141810266
NM_006514.3(SCN10A):c.5603A>C (p.His1868Pro) rs115463830
NM_006514.3(SCN10A):c.5605C>T (p.Arg1869Cys) rs141648641
NM_006514.3(SCN10A):c.853G>A (p.Glu285Lys) rs146151670
NM_006514.3(SCN10A):c.87T>C (p.Ala29=) rs148392780
NM_006514.3(SCN10A):c.969T>C (p.Tyr323=) rs143668889

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