ClinVar Miner

List of variants reported as likely benign for Long QT syndrome 11

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_005751.5(AKAP9):c.2425A>G (p.Ile809Val) rs144615758 0.00298
NM_005751.5(AKAP9):c.10858A>G (p.Ile3620Val) rs142729919 0.00296
NM_005751.5(AKAP9):c.6556T>C (p.Ser2186Pro) rs76177450 0.00250
NM_005751.5(AKAP9):c.11098-13T>G rs76709221 0.00235
NM_005751.5(AKAP9):c.510G>C (p.Glu170Asp) rs144888041 0.00212
NM_005751.5(AKAP9):c.5978-4A>G rs147494754 0.00175
NM_005751.5(AKAP9):c.10197T>C (p.Thr3399=) rs143627839 0.00148
NM_005751.5(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671 0.00142
NM_005751.5(AKAP9):c.80C>T (p.Ser27Leu) rs142401936 0.00137
NM_005751.5(AKAP9):c.288G>T (p.Glu96Asp) rs34953651 0.00112
NM_005751.5(AKAP9):c.10767G>A (p.Leu3589=) rs56198613 0.00111
NM_005751.5(AKAP9):c.9358+11T>C rs199714035 0.00101
NM_005751.5(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383 0.00093
NM_005751.5(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510 0.00089
NM_005751.5(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935 0.00082
NM_005751.5(AKAP9):c.6508-20A>T rs374874284 0.00079
NM_005751.5(AKAP9):c.10254G>C (p.Gln3418His) rs61757663 0.00065
NM_005751.5(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576 0.00061
NM_005751.5(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098 0.00061
NM_005751.5(AKAP9):c.4163C>T (p.Ser1388Leu) rs143565222 0.00034
NM_005751.5(AKAP9):c.8161-7G>A rs202218770 0.00019
NM_005751.5(AKAP9):c.7212C>T (p.Thr2404=) rs146854871 0.00014
NM_005751.5(AKAP9):c.610G>A (p.Asp204Asn) rs148920964 0.00011
NM_005751.5(AKAP9):c.8468A>G (p.Gln2823Arg) rs376528503 0.00008
NM_005751.5(AKAP9):c.261A>G (p.Leu87=) rs150736347 0.00006
NM_005751.5(AKAP9):c.6681A>G (p.Gln2227=) rs745898364 0.00006
NM_005751.5(AKAP9):c.6330+3A>G rs771419309 0.00005
NM_005751.5(AKAP9):c.5565A>G (p.Glu1855=) rs141094356 0.00003
NM_005751.5(AKAP9):c.1044A>C (p.Leu348=) rs747912745 0.00001
NM_005751.5(AKAP9):c.8052A>G (p.Glu2684=) rs878854810 0.00001
NM_005751.5(AKAP9):c.11682G>A (p.Gln3894=) rs769718964
NM_005751.5(AKAP9):c.4918-10dup rs755283199

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