ClinVar Miner

List of variants in gene KCNQ2 reported as likely benign for Early infantile epileptic encephalopathy

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Total variants: 47
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HGVS dbSNP
NM_172107.4(KCNQ2):c.1023+9A>G rs201787699
NM_172107.4(KCNQ2):c.1098G>A (p.Thr366=) rs758961686
NM_172107.4(KCNQ2):c.1119-4A>G rs749744963
NM_172107.4(KCNQ2):c.1224C>T (p.Asp408=) rs1060503977
NM_172107.4(KCNQ2):c.1232C>T (p.Pro411Leu) rs754682495
NM_172107.4(KCNQ2):c.1233G>A (p.Pro411=) rs757596960
NM_172107.4(KCNQ2):c.1239G>A (p.Pro413=) rs372146620
NM_172107.4(KCNQ2):c.1253G>T (p.Gly418Val) rs201750561
NM_172107.4(KCNQ2):c.126C>A (p.Ile42=) rs1555881817
NM_172107.4(KCNQ2):c.1301+7C>T rs374877247
NM_172107.4(KCNQ2):c.1301+8G>T rs532111320
NM_172107.4(KCNQ2):c.1348G>A (p.Val450Met) rs146492238
NM_172107.4(KCNQ2):c.1467C>T (p.Arg489=) rs767486470
NM_172107.4(KCNQ2):c.1503C>T (p.Ala501=) rs1801545
NM_172107.4(KCNQ2):c.1506G>A (p.Ala502=) rs780293757
NM_172107.4(KCNQ2):c.1539C>T (p.Pro513=) rs376713245
NM_172107.4(KCNQ2):c.1587C>T (p.Thr529=) rs753417293
NM_172107.4(KCNQ2):c.1631+8C>T rs1406473226
NM_172107.4(KCNQ2):c.1698C>T (p.Asp566=) rs768228902
NM_172107.4(KCNQ2):c.1764-6C>T rs118192239
NM_172107.4(KCNQ2):c.1776C>T (p.Ile592=) rs201868078
NM_172107.4(KCNQ2):c.1827C>T (p.Ala609=) rs369438374
NM_172107.4(KCNQ2):c.1866G>C (p.Arg622=) rs1060503976
NM_172107.4(KCNQ2):c.1914C>T (p.Asp638=) rs367845107
NM_172107.4(KCNQ2):c.1950C>T (p.Ile650=) rs772067813
NM_172107.4(KCNQ2):c.1998G>A (p.Pro666=) rs777059029
NM_172107.4(KCNQ2):c.2049C>T (p.His683=) rs150982653
NM_172107.4(KCNQ2):c.2052C>T (p.Gly684=) rs764444302
NM_172107.4(KCNQ2):c.2118C>T (p.Ala706=) rs777993694
NM_172107.4(KCNQ2):c.2229G>A (p.Pro743=) rs1481212168
NM_172107.4(KCNQ2):c.2244C>T (p.His748=) rs376327268
NM_172107.4(KCNQ2):c.2259C>T (p.Ser753=) rs749802787
NM_172107.4(KCNQ2):c.2280C>T (p.Arg760=) rs753696924
NM_172107.4(KCNQ2):c.2358G>A (p.Thr786=) rs559610397
NM_172107.4(KCNQ2):c.2373G>A (p.Pro791=) rs749958721
NM_172107.4(KCNQ2):c.2385C>T (p.His795=) rs143016981
NM_172107.4(KCNQ2):c.240C>T (p.Phe80=) rs961712229
NM_172107.4(KCNQ2):c.2571C>T (p.Thr857=) rs764525788
NM_172107.4(KCNQ2):c.2613G>T (p.Arg871Ser) rs587780369
NM_172107.4(KCNQ2):c.321C>T (p.Leu107=) rs757187562
NM_172107.4(KCNQ2):c.402C>T (p.Ile134=) rs140712277
NM_172107.4(KCNQ2):c.426C>T (p.Phe142=) rs780770793
NM_172107.4(KCNQ2):c.681C>T (p.Ala227=) rs1472366685
NM_172107.4(KCNQ2):c.690+9C>T rs369881492
NM_172107.4(KCNQ2):c.795G>A (p.Ala265=) rs148654588
NM_172107.4(KCNQ2):c.840C>T (p.Tyr280=) rs201556105
NM_172107.4(KCNQ2):c.900C>T (p.Ile300=) rs764404303

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