ClinVar Miner

List of variants reported as uncertain significance for Atrial fibrillation, familial, 7 by Illumina Clinical Services Laboratory,Illumina

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ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_002234.4(KCNA5):c.*244C>T
NM_002234.4(KCNA5):c.*493A>G rs886049577
NM_002234.4(KCNA5):c.*50G>A rs368484048
NM_002234.4(KCNA5):c.*558G>T
NM_002234.4(KCNA5):c.*782G>A rs189015926
NM_002234.4(KCNA5):c.*782G>C
NM_002234.4(KCNA5):c.-210G>C
NM_002234.4(KCNA5):c.-49G>C rs886049571
NM_002234.4(KCNA5):c.-52G>T
NM_002234.4(KCNA5):c.-85G>C
NM_002234.4(KCNA5):c.1210C>T (p.Leu404=) rs886049576
NM_002234.4(KCNA5):c.1329C>T (p.Ile443=) rs147209278
NM_002234.4(KCNA5):c.140A>G (p.Lys47Arg) rs886049573
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.1701G>A (p.Gly567=) rs771735295
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys) rs12720445
NM_002234.4(KCNA5):c.1789C>T (p.Arg597Trp)
NM_002234.4(KCNA5):c.186G>C (p.Ser62=)
NM_002234.4(KCNA5):c.231C>T (p.Pro77=)
NM_002234.4(KCNA5):c.251A>C (p.Glu84Ala) rs377036305
NM_002234.4(KCNA5):c.258A>C (p.Pro86=) rs886049574
NM_002234.4(KCNA5):c.268C>T (p.Arg90Trp)
NM_002234.4(KCNA5):c.36T>C (p.Gly12=) rs886049572
NM_002234.4(KCNA5):c.389G>A (p.Arg130His)
NM_002234.4(KCNA5):c.435C>A (p.Leu145=)
NM_002234.4(KCNA5):c.570C>T (p.Asn190=) rs12720444
NM_002234.4(KCNA5):c.602G>A (p.Arg201His)
NM_002234.4(KCNA5):c.615G>C (p.Leu205=) rs12720443
NM_002234.4(KCNA5):c.633G>C (p.Glu211Asp) rs35853292
NM_002234.4(KCNA5):c.701G>T (p.Arg234Leu) rs371521698
NM_002234.4(KCNA5):c.847C>T (p.Arg283Cys) rs886049575
NM_002234.4(KCNA5):c.898G>A (p.Gly300Ser) rs148708451
NM_002234.4(KCNA5):c.926G>A (p.Gly309Asp)
NM_002234.4(KCNA5):c.98A>T (p.Glu33Val) rs71584818

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