ClinVar Miner

List of variants in gene SCN5A reported by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 36
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HGVS dbSNP
NM_000335.4(SCN5A):c.1073T>C (p.Phe358Ser) rs876661391
NM_000335.4(SCN5A):c.1345A>G (p.Thr449Ala) rs199473571
NM_000335.4(SCN5A):c.1535C>T (p.Thr512Ile) rs199473118
NM_000335.4(SCN5A):c.1673A>G (p.His558Arg) rs1805124
NM_000335.4(SCN5A):c.1880C>T (p.Pro627Leu) rs778522112
NM_000335.4(SCN5A):c.1993G>T (p.Ala665Ser) rs756474485
NM_000335.4(SCN5A):c.2014G>A (p.Ala672Thr) rs199473140
NM_000335.4(SCN5A):c.2102C>T (p.Pro701Leu) rs199473147
NM_000335.4(SCN5A):c.2314G>A (p.Asp772Asn) rs199473157
NM_000335.4(SCN5A):c.2440C>T (p.Arg814Trp) rs199473161
NM_000335.4(SCN5A):c.268C>A (p.Gln90Lys) rs794728839
NM_000335.4(SCN5A):c.2735A>G (p.Gln912Arg) rs876661392
NM_000335.4(SCN5A):c.3464A>G (p.Asp1155Gly) rs747205537
NM_000335.4(SCN5A):c.3748G>A (p.Val1250Met) rs199473600
NM_000335.4(SCN5A):c.3820G>A (p.Asp1274Asn) rs137854618
NM_000335.4(SCN5A):c.3875T>C (p.Phe1292Ser) rs41311127
NM_000335.4(SCN5A):c.3908C>T (p.Thr1303Met) rs199473603
NM_000335.4(SCN5A):c.4267A>T (p.Ile1423Phe) rs757843082
NM_000335.4(SCN5A):c.4832T>A (p.Ile1611Asn) rs1553693063
NM_000335.4(SCN5A):c.4874G>A (p.Arg1625His) rs199473283
NM_000335.4(SCN5A):c.4928G>A (p.Arg1643His) rs28937316
NM_000335.4(SCN5A):c.4978G>A (p.Gly1660Arg) rs199473292
NM_000335.4(SCN5A):c.5126C>T (p.Ser1709Leu) rs137854604
NM_000335.4(SCN5A):c.52C>T (p.Arg18Trp) rs199473044
NM_000335.4(SCN5A):c.5333C>T (p.Thr1778Met) rs199473634
NM_000335.4(SCN5A):c.5347G>A (p.Glu1783Lys) rs137854601
NM_000335.4(SCN5A):c.5375T>A (p.Met1792Lys) rs794728897
NM_000335.4(SCN5A):c.5461_5464del (p.Glu1822fs) rs794728924
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.4(SCN5A):c.5870G>A (p.Arg1957Gln) rs199473331
NM_000335.4(SCN5A):c.5969G>A (p.Arg1990Gln) rs199473336
NM_000335.4(SCN5A):c.659C>T (p.Thr220Ile) rs45620037
NM_000335.4(SCN5A):c.680T>C (p.Leu227Pro) rs760011764
NM_000335.4(SCN5A):c.79C>T (p.Arg27Cys) rs746360906
NM_000335.4(SCN5A):c.80G>A (p.Arg27His) rs199473045
NM_000335.4(SCN5A):c.865G>A (p.Gly289Ser) rs199473084

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