ClinVar Miner

List of variants in gene KCNQ3 reported as uncertain significance for not provided

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Total variants: 62
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HGVS dbSNP
NM_004519.4(KCNQ3):c.1043C>T (p.Ala348Val) rs796052679
NM_004519.4(KCNQ3):c.1060G>T (p.Gly354Trp) rs796052680
NM_004519.4(KCNQ3):c.1077G>A (p.Val359=) rs750375617
NM_004519.4(KCNQ3):c.1226C>G (p.Pro409Arg) rs149272208
NM_004519.4(KCNQ3):c.127G>A (p.Val43Met) rs794726918
NM_004519.4(KCNQ3):c.1403A>G (p.Asn468Ser) rs118192252
NM_004519.4(KCNQ3):c.1421C>T (p.Thr474Met) rs757583944
NM_004519.4(KCNQ3):c.1458T>A (p.Ser486Arg) rs886043116
NM_004519.4(KCNQ3):c.1471G>A (p.Gly491Arg) rs201552546
NM_004519.4(KCNQ3):c.1507G>A (p.Gly503Arg) rs773584143
NM_004519.4(KCNQ3):c.1529A>C (p.Asp510Ala) rs1554622841
NM_004519.4(KCNQ3):c.1538C>T (p.Pro513Leu) rs768520561
NM_004519.4(KCNQ3):c.1543C>G (p.Leu515Val) rs368013249
NM_004519.4(KCNQ3):c.154C>G (p.Gln52Glu) rs1327292650
NM_004519.4(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496
NM_004519.4(KCNQ3):c.1591A>G (p.Lys531Glu) rs796052681
NM_004519.4(KCNQ3):c.1599dup (p.Phe534fs) rs762289015
NM_004519.4(KCNQ3):c.1694A>G (p.Gln565Arg) rs1003860988
NM_004519.4(KCNQ3):c.1709T>C (p.Met570Thr) rs199999939
NM_004519.4(KCNQ3):c.1715dup (p.Thr573fs) rs796052684
NM_004519.4(KCNQ3):c.1720C>A (p.Pro574Thr) rs74582884
NM_004519.4(KCNQ3):c.1722T>C (p.Pro574=) rs1554622049
NM_004519.4(KCNQ3):c.1783T>C (p.Ser595Pro) rs1064796743
NM_004519.4(KCNQ3):c.1850G>C (p.Ser617Thr) rs758002609
NM_004519.4(KCNQ3):c.1885G>A (p.Val629Ile) rs185511111
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111
NM_004519.4(KCNQ3):c.1885G>T (p.Val629Phe) rs185511111
NM_004519.4(KCNQ3):c.1918G>A (p.Val640Met) rs767903815
NM_004519.4(KCNQ3):c.1935A>G (p.Gln645=) rs587781011
NM_004519.4(KCNQ3):c.1945C>T (p.Arg649Trp) rs770863845
NM_004519.4(KCNQ3):c.1994C>T (p.Ser665Leu) rs147173555
NM_004519.4(KCNQ3):c.2035G>A (p.Asp679Asn) rs773672399
NM_004519.4(KCNQ3):c.2074C>G (p.Pro692Ala) rs1131691408
NM_004519.4(KCNQ3):c.2123G>T (p.Ser708Ile) rs977989588
NM_004519.4(KCNQ3):c.2128T>C (p.Tyr710His) rs181746838
NM_004519.4(KCNQ3):c.2144A>G (p.His715Arg) rs112314858
NM_004519.4(KCNQ3):c.2146G>C (p.Asp716His) rs149324120
NM_004519.4(KCNQ3):c.2194G>A (p.Ala732Thr) rs796052682
NM_004519.4(KCNQ3):c.2318G>A (p.Arg773Gln) rs769160647
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2338C>T (p.Arg780Cys) rs138852641
NM_004519.4(KCNQ3):c.2383G>A (p.Val795Ile) rs764544537
NM_004519.4(KCNQ3):c.2391C>T (p.His797=) rs763446963
NM_004519.4(KCNQ3):c.2443G>T (p.Asp815Tyr) rs530506549
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254
NM_004519.4(KCNQ3):c.2469dup (p.Ser824fs) rs886041208
NM_004519.4(KCNQ3):c.2537C>T (p.Thr846Met) rs765623435
NM_004519.4(KCNQ3):c.2545G>A (p.Gly849Ser) rs761201259
NM_004519.4(KCNQ3):c.2614A>G (p.Ile872Val) rs199682667
NM_004519.4(KCNQ3):c.293A>G (p.Lys98Arg) rs143194379
NM_004519.4(KCNQ3):c.330G>C (p.Leu110Phe) rs796052673
NM_004519.4(KCNQ3):c.477+5G>A rs373813381
NM_004519.4(KCNQ3):c.562C>T (p.Arg188Trp) rs754551218
NM_004519.4(KCNQ3):c.569G>A (p.Arg190Gln) rs796052674
NM_004519.4(KCNQ3):c.604+10G>T rs541587196
NM_004519.4(KCNQ3):c.788C>T (p.Thr263Met) rs1479652323
NM_004519.4(KCNQ3):c.856G>A (p.Val286Ile) rs549372035
NM_004519.4(KCNQ3):c.867G>A (p.Val289=)
NM_004519.4(KCNQ3):c.924G>A (p.Trp308Ter) rs1554627423
NM_004519.4(KCNQ3):c.954C>A (p.Gly318=) rs143224896
NM_004519.4(KCNQ3):c.956A>G (p.Tyr319Cys) rs1554627218
NM_004519.4(KCNQ3):c.997G>C (p.Ala333Pro) rs1064797349

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