ClinVar Miner

List of variants in gene SCN5A reported as pathogenic for Atrial fibrillation, familial, 10

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_000335.4(SCN5A):c.1282G>A (p.Glu428Lys) rs199473111
NM_000335.4(SCN5A):c.1333C>G (p.His445Asp) rs199473112
NM_000335.4(SCN5A):c.1410C>G (p.Asn470Lys) rs199473115
NM_000335.4(SCN5A):c.1963G>A (p.Glu655Lys) rs199473579
NM_000335.4(SCN5A):c.3820G>A (p.Asp1274Asn) rs137854618
NM_000335.4(SCN5A):c.5958C>A (p.Asn1986Lys) rs199473335
NM_001099404.1(SCN5A):c.615T>G (p.Tyr205Ter)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.