ClinVar Miner

List of variants in gene KCNA5 reported as likely benign for atrial fibrillation (disease)

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
NM_002234.3(KCNA5):c.*800G>A rs4625555
NM_002234.4(KCNA5):c.*508A>T rs1056468
NM_002234.4(KCNA5):c.*736A>T rs66942317
NM_002234.4(KCNA5):c.-167C>T rs3741930
NM_002234.4(KCNA5):c.1114C>T (p.Leu372=) rs1047059016
NM_002234.4(KCNA5):c.1149T>C (p.Gly383=) rs2359641
NM_002234.4(KCNA5):c.1539C>T (p.Pro513=) rs145832242
NM_002234.4(KCNA5):c.1595C>T (p.Pro532Leu) rs17221812
NM_002234.4(KCNA5):c.1672G>A (p.Gly558Arg) rs201328038
NM_002234.4(KCNA5):c.213_245del (p.Asp72_Pro82del) rs144879674
NM_002234.4(KCNA5):c.221G>A (p.Gly74Glu) rs555008698
NM_002234.4(KCNA5):c.36T>G (p.Gly12=) rs886049572
NM_002234.4(KCNA5):c.381C>T (p.Ser127=) rs45504599
NM_002234.4(KCNA5):c.464A>G (p.Tyr155Cys) rs202117321
NM_002234.4(KCNA5):c.633G>C (p.Glu211Asp) rs35853292
NM_002234.4(KCNA5):c.634C>T (p.Arg212Cys) rs77281462
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr) rs12720442
NM_002234.4(KCNA5):c.816G>A (p.Leu272=) rs775088698
NM_002234.4(KCNA5):c.898G>A (p.Gly300Ser) rs148708451
NM_002234.4(KCNA5):c.919C>T (p.Pro307Ser) rs17215409
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val) rs61737395
NM_002234.4(KCNA5):c.961G>A (p.Ala321Thr) rs765142607

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.