ClinVar Miner

List of variants in gene SCN5A reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 57
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HGVS dbSNP
NM_000335.4(SCN5A):c.1008G>A (p.Pro336=) rs200285003
NM_000335.4(SCN5A):c.1020G>T (p.Arg340=) rs727503410
NM_000335.4(SCN5A):c.1044C>T (p.Pro348=) rs370346797
NM_000335.4(SCN5A):c.1152C>T (p.Ser384=) rs372970828
NM_000335.4(SCN5A):c.1188C>T (p.Val396=) rs749683415
NM_000335.4(SCN5A):c.1195C>T (p.Leu399=) rs369253900
NM_000335.4(SCN5A):c.1336G>A (p.Glu446Lys) rs199473339
NM_000335.4(SCN5A):c.1347C>A (p.Thr449=) rs45477694
NM_000335.4(SCN5A):c.1441C>T (p.Arg481Trp) rs144511230
NM_000335.4(SCN5A):c.1479G>A (p.Arg493=) rs138870926
NM_000335.4(SCN5A):c.1538G>A (p.Arg513His) rs397517951
NM_000335.4(SCN5A):c.1653G>A (p.Ala551=) rs397517952
NM_000335.4(SCN5A):c.1659G>A (p.Glu553=) rs727503409
NM_000335.4(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_000335.4(SCN5A):c.1734C>T (p.Pro578=) rs200868190
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.1967C>T (p.Pro656Leu) rs41313681
NM_000335.4(SCN5A):c.2013C>T (p.Ser671=) rs751050999
NM_000335.4(SCN5A):c.2039G>A (p.Arg680His) rs199473142
NM_000335.4(SCN5A):c.2074C>A (p.Gln692Lys) rs45553235
NM_000335.4(SCN5A):c.2103G>A (p.Pro701=) rs564847999
NM_000335.4(SCN5A):c.2268C>T (p.Phe756=) rs372271677
NM_000335.4(SCN5A):c.2313C>T (p.Leu771=) rs876657580
NM_000335.4(SCN5A):c.2437-13C>T rs45455099
NM_000335.4(SCN5A):c.3408C>T (p.Ser1136=) rs553231555
NM_000335.4(SCN5A):c.3508+14C>A rs397516561
NM_000335.4(SCN5A):c.3663+10T>C rs200656652
NM_000335.4(SCN5A):c.369G>A (p.Ala123=) rs727504886
NM_000335.4(SCN5A):c.3870G>A (p.Leu1290=) rs41313033
NM_000335.4(SCN5A):c.3879C>T (p.Ala1293=) rs372132916
NM_000335.4(SCN5A):c.3904C>A (p.Arg1302=) rs200334972
NM_000335.4(SCN5A):c.4083G>A (p.Arg1361=) rs377173580
NM_000335.4(SCN5A):c.4209C>T (p.Asn1403=) rs397517954
NM_000335.4(SCN5A):c.4296+10C>T rs1553694579
NM_000335.4(SCN5A):c.4297-14T>C rs56104887
NM_000335.4(SCN5A):c.4299T>C (p.Tyr1433=) rs200556220
NM_000335.4(SCN5A):c.456C>T (p.Asp152=) rs190803993
NM_000335.4(SCN5A):c.4695C>G (p.Leu1565=) rs727505094
NM_000335.4(SCN5A):c.4821C>T (p.Leu1607=) rs45437099
NM_000335.4(SCN5A):c.4857G>A (p.Thr1619=) rs753174463
NM_000335.4(SCN5A):c.5061C>T (p.Ile1687=) rs145731678
NM_000335.4(SCN5A):c.5199C>T (p.Asn1733=) rs368980118
NM_000335.4(SCN5A):c.5478C>T (p.Ile1826=) rs138892850
NM_000335.4(SCN5A):c.5604C>T (p.Asp1868=) rs560476223
NM_000335.4(SCN5A):c.567T>C (p.Leu189=) rs876657581
NM_000335.4(SCN5A):c.5793G>A (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5799C>T (p.Ser1933=) rs375254452
NM_000335.4(SCN5A):c.5946C>T (p.Ala1982=) rs397517957
NM_000335.4(SCN5A):c.6000C>T (p.Leu2000=) rs538707712
NM_000335.4(SCN5A):c.6007T>C (p.Phe2003Leu) rs41311117
NM_000335.4(SCN5A):c.6013C>G (p.Pro2005Ala) rs45489199
NM_000335.4(SCN5A):c.630G>A (p.Val210=) rs193922727
NM_000335.4(SCN5A):c.659C>T (p.Thr220Ile) rs45620037
NM_000335.4(SCN5A):c.72C>T (p.Ile24=) rs727503412
NM_000335.4(SCN5A):c.756T>C (p.Asp252=) rs397517958
NM_000335.4(SCN5A):c.856G>T (p.Ala286Ser) rs61746118
NM_000335.4(SCN5A):c.954C>T (p.Asn318=) rs372623225

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