ClinVar Miner

List of variants in gene KCNQ3 studied for not provided

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Total variants: 78
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HGVS dbSNP
GRCh37/hg19 8q24.22(chr8:133226397-133306801)x1
NM_001204824.1(KCNQ3):c.-32977G>C rs796052673
NM_001204824.1(KCNQ3):c.-33014A>G rs143194379
NM_001204824.1(KCNQ3):c.1043A>G (p.Asn348Ser) rs118192252
NM_001204824.1(KCNQ3):c.1061C>T (p.Thr354Met) rs757583944
NM_001204824.1(KCNQ3):c.1147G>A (p.Gly383Arg) rs773584143
NM_001204824.1(KCNQ3):c.117+5G>A rs373813381
NM_001204824.1(KCNQ3):c.1178C>T (p.Pro393Leu) rs768520561
NM_001204824.1(KCNQ3):c.1231A>G (p.Lys411Glu) rs796052681
NM_001204824.1(KCNQ3):c.1360C>A (p.Pro454Thr) rs74582884
NM_001204824.1(KCNQ3):c.1490G>C (p.Ser497Thr) rs758002609
NM_001204824.1(KCNQ3):c.1525G>T (p.Val509Phe) rs185511111
NM_001204824.1(KCNQ3):c.1575A>G (p.Gln525=) rs587781011
NM_001204824.1(KCNQ3):c.1768T>C (p.Tyr590His) rs181746838
NM_001204824.1(KCNQ3):c.1784A>G (p.His595Arg) rs112314858
NM_001204824.1(KCNQ3):c.1834G>A (p.Ala612Thr) rs796052682
NM_001204824.1(KCNQ3):c.1970G>A (p.Arg657Gln) rs201328910
NM_001204824.1(KCNQ3):c.1991G>A (p.Arg664Gln) rs754896169
NM_001204824.1(KCNQ3):c.202C>T (p.Arg68Trp) rs754551218
NM_001204824.1(KCNQ3):c.2083G>T (p.Asp695Tyr) rs530506549
NM_001204824.1(KCNQ3):c.2254A>G (p.Ile752Val) rs199682667
NM_001204824.1(KCNQ3):c.437A>G (p.Tyr146Cys) rs796052677
NM_001204824.1(KCNQ3):c.553G>T (p.Asp185Tyr) rs1085307996
NM_001204824.1(KCNQ3):c.557C>T (p.Ala186Val) rs796052678
NM_001204824.1(KCNQ3):c.563G>C (p.Trp188Ser) rs1064794632
NM_001204824.1(KCNQ3):c.594C>A (p.Gly198=) rs143224896
NM_001204824.1(KCNQ3):c.683C>T (p.Ala228Val) rs796052679
NM_001204824.1(KCNQ3):c.700G>T (p.Gly234Trp) rs796052680
NM_001204824.1(KCNQ3):c.717G>A (p.Val239=) rs750375617
NM_001204824.1(KCNQ3):c.866C>G (p.Pro289Arg) rs149272208
NM_004519.2(KCNQ3):c.679C>T (p.Arg227Ter) rs796052675
NM_004519.3(KCNQ3):c.1060G>A (p.Gly354Arg) rs796052680
NM_004519.3(KCNQ3):c.1067C>T (p.Ala356Val) rs1554627025
NM_004519.3(KCNQ3):c.127G>A (p.Val43Met) rs794726918
NM_004519.3(KCNQ3):c.1458T>A (p.Ser486Arg) rs886043116
NM_004519.3(KCNQ3):c.1471G>A (p.Gly491Arg) rs201552546
NM_004519.3(KCNQ3):c.1529A>C (p.Asp510Ala) rs1554622841
NM_004519.3(KCNQ3):c.1543C>G (p.Leu515Val) rs368013249
NM_004519.3(KCNQ3):c.154C>G (p.Gln52Glu) rs1327292650
NM_004519.3(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496
NM_004519.3(KCNQ3):c.1568+12A>G rs181790623
NM_004519.3(KCNQ3):c.1599dupA (p.Phe534Ilefs) rs762289015
NM_004519.3(KCNQ3):c.1694A>G (p.Gln565Arg) rs1003860988
NM_004519.3(KCNQ3):c.1700+3G>A rs115092422
NM_004519.3(KCNQ3):c.1709T>C (p.Met570Thr) rs199999939
NM_004519.3(KCNQ3):c.1715dupT (p.Thr573Hisfs) rs796052684
NM_004519.3(KCNQ3):c.1722T>C (p.Pro574=) rs1554622049
NM_004519.3(KCNQ3):c.1783T>C (p.Ser595Pro) rs1064796743
NM_004519.3(KCNQ3):c.1885G>A (p.Val629Ile) rs185511111
NM_004519.3(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111
NM_004519.3(KCNQ3):c.1918G>A (p.Val640Met) rs767903815
NM_004519.3(KCNQ3):c.1945C>T (p.Arg649Trp) rs770863845
NM_004519.3(KCNQ3):c.1994C>T (p.Ser665Leu) rs147173555
NM_004519.3(KCNQ3):c.2035G>A (p.Asp679Asn) rs773672399
NM_004519.3(KCNQ3):c.2074C>G (p.Pro692Ala) rs1131691408
NM_004519.3(KCNQ3):c.2123G>T (p.Ser708Ile) rs977989588
NM_004519.3(KCNQ3):c.2146G>C (p.Asp716His) rs149324120
NM_004519.3(KCNQ3):c.2306C>A (p.Pro769His) rs114095081
NM_004519.3(KCNQ3):c.2318G>A (p.Arg773Gln) rs769160647
NM_004519.3(KCNQ3):c.2338C>T (p.Arg780Cys) rs138852641
NM_004519.3(KCNQ3):c.2383G>A (p.Val795Ile) rs764544537
NM_004519.3(KCNQ3):c.2391C>T (p.His797=) rs763446963
NM_004519.3(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254
NM_004519.3(KCNQ3):c.2469dupG (p.Ser824Valfs) rs886041208
NM_004519.3(KCNQ3):c.2537C>T (p.Thr846Met) rs765623435
NM_004519.3(KCNQ3):c.2545G>A (p.Gly849Ser) rs761201259
NM_004519.3(KCNQ3):c.604+10G>T rs541587196
NM_004519.3(KCNQ3):c.688C>T (p.Arg230Cys) rs796052676
NM_004519.3(KCNQ3):c.689G>A (p.Arg230His) rs749205120
NM_004519.3(KCNQ3):c.788C>T (p.Thr263Met) rs1479652323
NM_004519.3(KCNQ3):c.856G>A (p.Val286Ile) rs549372035
NM_004519.3(KCNQ3):c.867G>A (p.Val289=)
NM_004519.3(KCNQ3):c.878G>A (p.Gly293Glu) rs1064795142
NM_004519.3(KCNQ3):c.924G>A (p.Trp308Ter) rs1554627423
NM_004519.3(KCNQ3):c.956A>G (p.Tyr319Cys) rs1554627218
NM_004519.3(KCNQ3):c.997G>C (p.Ala333Pro) rs1064797349
NM_004519.4(KCNQ3):c.569G>A (p.Arg190Gln) rs796052674
NM_004519.4(KCNQ3):c.994A>T (p.Ile332Phe)

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