ClinVar Miner

List of variants in gene KCNH2 reported as benign by Color

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Total variants: 35
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HGVS dbSNP
NM_000238.4(KCNH2):c.1128+1776G>T
NM_000238.4(KCNH2):c.1467C>T (p.Ile489=) rs740952
NM_000238.4(KCNH2):c.1539C>T (p.Phe513=) rs1805120
NM_000238.4(KCNH2):c.1563C>T (p.Ile521=) rs143011005
NM_000238.4(KCNH2):c.1692A>G (p.Leu564=) rs1805121
NM_000238.4(KCNH2):c.1956T>C (p.Tyr652=) rs1137617
NM_000238.4(KCNH2):c.2412C>A (p.Ile804=)
NM_000238.4(KCNH2):c.2454G>A (p.Ser818=) rs72549418
NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr) rs1805123
NM_000238.4(KCNH2):c.3111C>T (p.Asp1037=) rs200799870
NM_000238.4(KCNH2):c.3153-15C>T rs41313755
NM_000238.4(KCNH2):c.3331-13GT[2] rs41313749
NM_000238.4(KCNH2):c.442C>T (p.Arg148Trp) rs139544114
NM_172056.2(KCNH2):c.1128+1784C>T rs371509270
NM_172056.2(KCNH2):c.1332G>A (p.Glu444=) rs9770044
NM_172056.2(KCNH2):c.1353G>A (p.Pro451=) rs763446458
NM_172056.2(KCNH2):c.1528C>T (p.Leu510=) rs75648145
NM_172056.2(KCNH2):c.1558-5C>T rs114186001
NM_172056.2(KCNH2):c.1581G>A (p.Ala527=) rs150275982
NM_172056.2(KCNH2):c.1800C>T (p.Ser600=) rs143518632
NM_172056.2(KCNH2):c.1809C>T (p.Gly603=) rs41314375
NM_172056.2(KCNH2):c.1887C>T (p.Asn629=) rs41307295
NM_172056.2(KCNH2):c.1923C>T (p.Ser641=) rs142249065
NM_172056.2(KCNH2):c.2503del (p.Leu835fs) rs546898924
NM_172056.2(KCNH2):c.2553C>A (p.Ser851Arg) rs536958259
NM_172056.2(KCNH2):c.2576C>T (p.Thr859Met) rs41314366
NM_172056.2(KCNH2):c.300G>T (p.Arg100=) rs761176105
NM_172056.2(KCNH2):c.441C>T (p.His147=) rs143479939
NM_172056.2(KCNH2):c.77-5C>G rs72549419
NM_172057.2(KCNH2):c.2043C>T (p.Ser681=) rs199767579
NM_172057.2(KCNH2):c.2113C>T (p.Leu705Phe) rs199473025
NM_172057.2(KCNH2):c.2120G>T (p.Arg707Leu) rs36210421
NM_172057.2(KCNH2):c.2133-4C>T rs181119727
NM_172057.2(KCNH2):c.2196G>A (p.Thr732=) rs200182770
NM_172057.2(KCNH2):c.2208C>T (p.Pro736=) rs41312087

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