ClinVar Miner

List of variants in gene SCN5A reported as likely benign by Color

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Total variants: 65
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HGVS dbSNP
NM_000335.4(SCN5A):c.1008G>A (p.Pro336=) rs200285003
NM_000335.4(SCN5A):c.1044C>T (p.Pro348=) rs370346797
NM_000335.4(SCN5A):c.1095C>G (p.Leu365=) rs370377886
NM_000335.4(SCN5A):c.1152C>T (p.Ser384=) rs372970828
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.1353G>A (p.Arg451=) rs1258339684
NM_000335.4(SCN5A):c.1365C>T (p.Thr455=) rs747138429
NM_000335.4(SCN5A):c.15A>G (p.Leu5=) rs747382316
NM_000335.4(SCN5A):c.1653G>T (p.Ala551=) rs397517952
NM_000335.4(SCN5A):c.1755C>T (p.His585=) rs201024847
NM_000335.4(SCN5A):c.1881G>A (p.Pro627=) rs1027656721
NM_000335.4(SCN5A):c.1944G>A (p.Pro648=) rs773792853
NM_000335.4(SCN5A):c.1967C>T (p.Pro656Leu) rs41313681
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.2181C>T (p.Ile727=) rs186942072
NM_000335.4(SCN5A):c.2263-12C>T rs768759826
NM_000335.4(SCN5A):c.2361C>T (p.Ile787=) rs780897743
NM_000335.4(SCN5A):c.2437-13C>T rs45455099
NM_000335.4(SCN5A):c.2437-5C>A rs72549411
NM_000335.4(SCN5A):c.2440C>A (p.Arg814=) rs199473161
NM_000335.4(SCN5A):c.2484C>T (p.Leu828=) rs923903065
NM_000335.4(SCN5A):c.2496C>T (p.Ile832=) rs761287478
NM_000335.4(SCN5A):c.3468C>T (p.Leu1156=) rs570719978
NM_000335.4(SCN5A):c.3536C>T (p.Ala1179Val) rs41310765
NM_000335.4(SCN5A):c.3537G>A (p.Ala1179=) rs370990219
NM_000335.4(SCN5A):c.3724G>A (p.Asp1242Asn) rs199473599
NM_000335.4(SCN5A):c.373G>C (p.Val125Leu) rs199473059
NM_000335.4(SCN5A):c.3795C>T (p.Tyr1265=) rs371610895
NM_000335.4(SCN5A):c.3837C>T (p.Asp1279=) rs749069817
NM_000335.4(SCN5A):c.3875T>C (p.Phe1292Ser) rs41311127
NM_000335.4(SCN5A):c.393-5C>T rs368678204
NM_000335.4(SCN5A):c.3984C>T (p.Gly1328=) rs761384669
NM_000335.4(SCN5A):c.4071G>A (p.Gly1357=) rs780532060
NM_000335.4(SCN5A):c.4098A>G (p.Thr1366=) rs563832893
NM_000335.4(SCN5A):c.4297-9C>T rs1410235393
NM_000335.4(SCN5A):c.4401C>T (p.Val1467=) rs766197312
NM_000335.4(SCN5A):c.4467G>A (p.Glu1489=) rs375026424
NM_000335.4(SCN5A):c.4506C>T (p.Ser1502=) rs45548237
NM_000335.4(SCN5A):c.456C>T (p.Asp152=) rs190803993
NM_000335.4(SCN5A):c.4806C>T (p.Ile1602=) rs769709544
NM_000335.4(SCN5A):c.4854G>A (p.Pro1618=) rs368031564
NM_000335.4(SCN5A):c.5088C>T (p.Phe1696=) rs762929897
NM_000335.4(SCN5A):c.52C>T (p.Arg18Trp) rs199473044
NM_000335.4(SCN5A):c.5328G>A (p.Val1776=) rs1559721151
NM_000335.4(SCN5A):c.5334G>A (p.Thr1778=) rs41311121
NM_000335.4(SCN5A):c.5793G>C (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5799C>T (p.Ser1933=) rs375254452
NM_000335.4(SCN5A):c.5882C>T (p.Pro1961Leu) rs199473638
NM_000335.4(SCN5A):c.5972G>C (p.Gly1991Ala) rs558904601
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.612-9T>A rs1229946415
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.801C>T (p.Ile267=) rs45587735
NM_000335.4(SCN5A):c.885G>A (p.Glu295=) rs373342830
NM_000335.4(SCN5A):c.888C>T (p.Ala296=) rs774132896
NM_000335.4(SCN5A):c.891C>T (p.Asp297=) rs529144420
NM_000335.4(SCN5A):c.954C>T (p.Asn318=) rs372623225
NM_000335.4(SCN5A):c.993C>T (p.Asp331=) rs757715398
NM_001099404.1(SCN5A):c.648G>A (p.Ser216=) rs45475402
NM_001099404.1(SCN5A):c.672G>A (p.Leu224=) rs1559782119

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