ClinVar Miner

List of variants in gene SCN5A reported as benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_000335.4(SCN5A):c.1152C>T (p.Ser384=) rs372970828
NM_000335.4(SCN5A):c.1236C>T (p.Val412=) rs45565936
NM_000335.4(SCN5A):c.1587T>C (p.Ile529=) rs45624133
NM_000335.4(SCN5A):c.1681C>T (p.Leu561=) rs45522138
NM_000335.4(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.2436+12G>A rs41312419
NM_000335.4(SCN5A):c.2437-5C>A rs72549411
NM_000335.4(SCN5A):c.3508+10C>T rs41258454
NM_000335.4(SCN5A):c.3951G>A (p.Glu1317=) rs769473892
NM_000335.4(SCN5A):c.4215G>A (p.Gly1405=) rs41311123
NM_000335.4(SCN5A):c.4506C>T (p.Ser1502=) rs45548237
NM_000335.4(SCN5A):c.5709G>A (p.Ser1903=) rs376826051
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.4(SCN5A):c.630G>A (p.Val210=) rs193922727
NM_000335.4(SCN5A):c.717C>T (p.Ile239=) rs41285129

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