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
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HGVS dbSNP
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

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