ClinVar Miner

List of variants in gene KCNA5 reported as likely benign for Atrial fibrillation, familial, 7

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Total variants: 82
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HGVS dbSNP
NM_002234.4(KCNA5):c.*543G>C
NM_002234.4(KCNA5):c.1005C>T (p.Phe335=) rs1056432511
NM_002234.4(KCNA5):c.1011C>T (p.Phe337=) rs977096843
NM_002234.4(KCNA5):c.1114C>T (p.Leu372=) rs1047059016
NM_002234.4(KCNA5):c.1149T>G (p.Gly383=)
NM_002234.4(KCNA5):c.1150G>A (p.Gly384Arg) rs76708779
NM_002234.4(KCNA5):c.1233C>T (p.Phe411=) rs201975625
NM_002234.4(KCNA5):c.1242C>G (p.Ser414=)
NM_002234.4(KCNA5):c.1242C>T (p.Ser414=)
NM_002234.4(KCNA5):c.1287C>A (p.Ala429=)
NM_002234.4(KCNA5):c.1329C>A (p.Ile443=)
NM_002234.4(KCNA5):c.1329C>T (p.Ile443=) rs147209278
NM_002234.4(KCNA5):c.135G>A (p.Gly45=)
NM_002234.4(KCNA5):c.1386C>T (p.Thr462=)
NM_002234.4(KCNA5):c.1407C>T (p.Asp469=)
NM_002234.4(KCNA5):c.1449C>T (p.Tyr483=)
NM_002234.4(KCNA5):c.1485C>A (p.Ile495=)
NM_002234.4(KCNA5):c.1497G>A (p.Leu499=) rs17221805
NM_002234.4(KCNA5):c.1509C>T (p.Ala503=) rs748151274
NM_002234.4(KCNA5):c.1539C>G (p.Pro513=)
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.1596G>A (p.Pro532=)
NM_002234.4(KCNA5):c.1608G>A (p.Lys536=)
NM_002234.4(KCNA5):c.162C>T (p.Arg54=)
NM_002234.4(KCNA5):c.1638G>A (p.Pro546=)
NM_002234.4(KCNA5):c.1650A>G (p.Arg550=) rs762958451
NM_002234.4(KCNA5):c.1662G>C (p.Arg554=)
NM_002234.4(KCNA5):c.1672G>A (p.Gly558Arg) rs201328038
NM_002234.4(KCNA5):c.1701G>A (p.Gly567=) rs771735295
NM_002234.4(KCNA5):c.1707C>A (p.Thr569=)
NM_002234.4(KCNA5):c.1713G>A (p.Glu571=) rs147455567
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys) rs12720445
NM_002234.4(KCNA5):c.1764C>T (p.Val588=)
NM_002234.4(KCNA5):c.1790G>A (p.Arg597Gln) rs201342234
NM_002234.4(KCNA5):c.1797C>G (p.Ser599=)
NM_002234.4(KCNA5):c.180G>A (p.Ala60=) rs376660949
NM_002234.4(KCNA5):c.186G>C (p.Ser62=)
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.229C>T (p.Pro77Ser) rs202083721
NM_002234.4(KCNA5):c.251A>C (p.Glu84Ala) rs377036305
NM_002234.4(KCNA5):c.291G>A (p.Glu97=)
NM_002234.4(KCNA5):c.342G>C (p.Thr114=)
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.390C>T (p.Arg130=)
NM_002234.4(KCNA5):c.402G>A (p.Gln134=)
NM_002234.4(KCNA5):c.464A>G (p.Tyr155Cys) rs202117321
NM_002234.4(KCNA5):c.543C>T (p.Ser181=) rs750031654
NM_002234.4(KCNA5):c.544G>A (p.Gly182Arg) rs755408841
NM_002234.4(KCNA5):c.549C>T (p.Gly183=)
NM_002234.4(KCNA5):c.561G>A (p.Arg187=)
NM_002234.4(KCNA5):c.624G>A (p.Glu208=)
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.651G>A (p.Glu217=)
NM_002234.4(KCNA5):c.675G>A (p.Lys225=) rs142095205
NM_002234.4(KCNA5):c.690C>T (p.Asn230=)
NM_002234.4(KCNA5):c.717C>T (p.Ile239=)
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr) rs12720442
NM_002234.4(KCNA5):c.78C>T (p.Cys26=) rs376836489
NM_002234.4(KCNA5):c.795C>T (p.Ile265=)
NM_002234.4(KCNA5):c.797C>T (p.Thr266Ile) rs369750762
NM_002234.4(KCNA5):c.79G>A (p.Gly27Ser) rs201238766
NM_002234.4(KCNA5):c.804C>T (p.Cys268=)
NM_002234.4(KCNA5):c.816G>A (p.Leu272=) rs775088698
NM_002234.4(KCNA5):c.828G>A (p.Arg276=) rs765528663
NM_002234.4(KCNA5):c.843G>A (p.Leu281=) rs755035314
NM_002234.4(KCNA5):c.852C>T (p.His284=)
NM_002234.4(KCNA5):c.859G>T (p.Ala287Ser) rs149582940
NM_002234.4(KCNA5):c.860C>T (p.Ala287Val) rs144246051
NM_002234.4(KCNA5):c.86C>A (p.Ala29Asp) rs763281934
NM_002234.4(KCNA5):c.897C>T (p.Asn299=)
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.929C>T (p.Pro310Leu) rs17215402
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val) rs61737395
NM_002234.4(KCNA5):c.933G>A (p.Thr311=)
NM_002234.4(KCNA5):c.945C>A (p.Leu315=)
NM_002234.4(KCNA5):c.960G>A (p.Leu320=) rs546959674
NM_002234.4(KCNA5):c.961G>A (p.Ala321Thr) rs765142607

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