ClinVar Miner

List of variants in gene KCNH2 reported by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 29
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HGVS dbSNP
NM_172056.2(KCNH2):c.1039C>T (p.Pro347Ser) rs138776684
NM_172056.2(KCNH2):c.1128G>A (p.Gln376=) rs770047651
NM_172056.2(KCNH2):c.1496T>G (p.Leu499Arg) rs794728370
NM_172056.2(KCNH2):c.1655T>C (p.Leu552Ser) rs199472918
NM_172056.2(KCNH2):c.1682C>T (p.Ala561Val) rs121912504
NM_172056.2(KCNH2):c.1714G>A (p.Gly572Ser) rs9333649
NM_172056.2(KCNH2):c.1805T>C (p.Leu602Pro) rs876661348
NM_172056.2(KCNH2):c.1838C>T (p.Thr613Met) rs199473524
NM_172056.2(KCNH2):c.1882G>A (p.Gly628Ser) rs121912507
NM_172056.2(KCNH2):c.215C>A (p.Pro72Gln) rs199473421
NM_172056.2(KCNH2):c.2254C>T (p.Arg752Trp) rs199472990
NM_172056.2(KCNH2):c.2390C>A (p.Ala797Asp) rs794728389
NM_172056.2(KCNH2):c.26C>T (p.Ala9Val) rs775317201
NM_172056.2(KCNH2):c.422C>T (p.Pro141Leu) rs199472864
NM_172056.2(KCNH2):c.442C>T (p.Arg148Trp) rs139544114
NM_172056.2(KCNH2):c.545C>G (p.Ser182Trp) rs1057517742
NM_172056.2(KCNH2):c.652A>G (p.Met218Val) rs199472869
NM_172056.2(KCNH2):c.982C>T (p.Arg328Cys) rs199473505
NM_172057.2(KCNH2):c.1447C>T (p.Arg483Trp) rs199473538
NM_172057.2(KCNH2):c.1606G>A (p.Glu536Lys) rs1554424688
NM_172057.2(KCNH2):c.1645T>G (p.Leu549Val) rs765427343
NM_172057.2(KCNH2):c.1670A>C (p.Lys557Thr) rs1805123
NM_172057.2(KCNH2):c.1760G>T (p.Trp587Leu) rs794728399
NM_172057.2(KCNH2):c.1928C>T (p.Thr643Ile) rs149955375
NM_172057.2(KCNH2):c.2020C>T (p.Arg674Ter) rs794728403
NM_172057.2(KCNH2):c.2075_2079dup (p.Pro694fs) rs794728467
NM_172057.2(KCNH2):c.2079_2089del (p.Pro694fs) rs794728466
NM_172057.2(KCNH2):c.2258C>T (p.Pro753Leu) rs199473545
NM_172057.2(KCNH2):c.2345C>G (p.Pro782Arg) rs531460655

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