ClinVar Miner

List of variants in gene SCN5A reported as uncertain significance for Arrhythmia

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Total variants: 53
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HGVS dbSNP
NM_000335.4(SCN5A):c.1051G>A (p.Gly351Ser) rs201276017
NM_000335.4(SCN5A):c.1273G>A (p.Ala425Thr) rs761117662
NM_000335.4(SCN5A):c.1519-15T>A rs1386092614
NM_000335.4(SCN5A):c.1597C>T (p.Arg533Cys)
NM_000335.4(SCN5A):c.1606G>C (p.Asp536His) rs1475895120
NM_000335.4(SCN5A):c.1700T>A (p.Leu567Gln) rs199473124
NM_000335.4(SCN5A):c.1828G>A (p.Glu610Lys) rs751774111
NM_000335.4(SCN5A):c.1855C>T (p.Leu619Phe) rs199473133
NM_000335.4(SCN5A):c.1858C>T (p.Arg620Cys) rs199473577
NM_000335.4(SCN5A):c.1873G>C (p.Glu625Gln) rs201552126
NM_000335.4(SCN5A):c.1943C>T (p.Pro648Leu) rs45609733
NM_000335.4(SCN5A):c.1993G>A (p.Ala665Thr) rs756474485
NM_000335.4(SCN5A):c.1993G>T (p.Ala665Ser) rs756474485
NM_000335.4(SCN5A):c.2244G>C (p.Met748Ile) rs1424832911
NM_000335.4(SCN5A):c.2403G>A (p.Met801Ile) rs1559758625
NM_000335.4(SCN5A):c.2422C>T (p.Arg808Cys) rs749864465
NM_000335.4(SCN5A):c.2630C>G (p.Pro877Arg) rs1060501147
NM_000335.4(SCN5A):c.3456G>C (p.Gln1152His) rs776705132
NM_000335.4(SCN5A):c.3521G>A (p.Arg1174His) rs374314562
NM_000335.4(SCN5A):c.3538G>T (p.Val1180Leu) rs794728874
NM_000335.4(SCN5A):c.3557C>A (p.Pro1186Gln) rs199473201
NM_000335.4(SCN5A):c.3680A>C (p.Tyr1227Ser) rs746509665
NM_000335.4(SCN5A):c.368C>T (p.Ala123Val)
NM_000335.4(SCN5A):c.3715G>C (p.Glu1239Gln) rs199473211
NM_000335.4(SCN5A):c.3832G>A (p.Val1278Ile) rs199473341
NM_000335.4(SCN5A):c.3908C>T (p.Thr1303Met) rs199473603
NM_000335.4(SCN5A):c.4289C>G (p.Ser1430Cys) rs1226701514
NM_000335.4(SCN5A):c.4313A>G (p.Gln1438Arg) rs1350022850
NM_000335.4(SCN5A):c.436G>A (p.Val146Met) rs199473061
NM_000335.4(SCN5A):c.4498C>G (p.Leu1500Val) rs199473266
NM_000335.4(SCN5A):c.44G>C (p.Arg15Thr) rs373410109
NM_000335.4(SCN5A):c.476A>G (p.Tyr159Cys) rs767116750
NM_000335.4(SCN5A):c.4864C>A (p.Arg1622=) rs137854613
NM_000335.4(SCN5A):c.4975A>G (p.Ile1659Val) rs199473625
NM_000335.4(SCN5A):c.5035G>A (p.Ala1679Thr) rs199473294
NM_000335.4(SCN5A):c.5182G>A (p.Asp1728Asn) rs763880032
NM_000335.4(SCN5A):c.5269A>G (p.Ile1757Val) rs1325549884
NM_000335.4(SCN5A):c.5326G>A (p.Val1776Met) rs199473314
NM_000335.4(SCN5A):c.5403C>G (p.Asp1801Glu) rs1367727373
NM_000335.4(SCN5A):c.5510T>A (p.Met1837Lys) rs1559720415
NM_000335.4(SCN5A):c.5524G>C (p.Val1842Leu) rs1559720356
NM_000335.4(SCN5A):c.5576G>A (p.Arg1859Lys) rs1559720220
NM_000335.4(SCN5A):c.569G>A (p.Arg190Gln) rs199473069
NM_000335.4(SCN5A):c.5800G>A (p.Gly1934Ser) rs199473637
NM_000335.4(SCN5A):c.5935G>T (p.Val1979Phe) rs772258197
NM_000335.4(SCN5A):c.5965G>C (p.Val1989Leu) rs765885732
NM_000335.4(SCN5A):c.6020C>T (p.Pro2007Leu) rs750070697
NM_000335.4(SCN5A):c.6031C>T (p.Arg2011Cys) rs199473640
NM_000335.4(SCN5A):c.647C>T (p.Ser216Leu) rs41276525
NM_000335.4(SCN5A):c.718G>A (p.Val240Met) rs199473076
NM_000335.4(SCN5A):c.784A>G (p.Ser262Gly) rs777689378
NM_000335.4(SCN5A):c.82A>T (p.Met28Leu) rs748805919
NM_000335.4(SCN5A):c.880G>A (p.Val294Met) rs199473086

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