ClinVar Miner

List of variants in gene KCNQ3 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111 0.00016
NM_004519.4(KCNQ3):c.562C>T (p.Arg188Trp) rs754551218 0.00006
NM_004519.4(KCNQ3):c.856G>A (p.Val286Ile) rs549372035 0.00006
NM_004519.4(KCNQ3):c.1697C>T (p.Thr566Met) rs746403693 0.00004
NM_004519.4(KCNQ3):c.1411C>T (p.Arg471Cys) rs753513804 0.00003
NM_004519.4(KCNQ3):c.1543C>G (p.Leu515Val) rs368013249 0.00003
NM_004519.4(KCNQ3):c.2443G>T (p.Asp815Tyr) rs530506549 0.00003
NM_004519.4(KCNQ3):c.1471G>A (p.Gly491Arg) rs201552546 0.00002
NM_004519.4(KCNQ3):c.1507G>A (p.Gly503Arg) rs773584143 0.00002
NM_004519.4(KCNQ3):c.1706A>G (p.Asp569Gly) rs372671883 0.00002
NM_004519.4(KCNQ3):c.2329C>T (p.Arg777Trp) rs776128068 0.00002
NM_004519.4(KCNQ3):c.2383G>A (p.Val795Ile) rs764544537 0.00002
NM_004519.4(KCNQ3):c.1118A>C (p.Lys373Thr) rs1418558443 0.00001
NM_004519.4(KCNQ3):c.1399A>G (p.Asn467Asp) rs1825285200 0.00001
NM_004519.4(KCNQ3):c.1421C>T (p.Thr474Met) rs757583944 0.00001
NM_004519.4(KCNQ3):c.1538C>T (p.Pro513Leu) rs768520561 0.00001
NM_004519.4(KCNQ3):c.1562C>G (p.Ala521Gly) rs1057518505 0.00001
NM_004519.4(KCNQ3):c.1709T>C (p.Met570Thr) rs199999939 0.00001
NM_004519.4(KCNQ3):c.1918G>A (p.Val640Met) rs767903815 0.00001
NM_004519.4(KCNQ3):c.2123G>T (p.Ser708Ile) rs977989588 0.00001
NM_004519.4(KCNQ3):c.2269C>T (p.Arg757Ter) rs779444430 0.00001
NM_004519.4(KCNQ3):c.2434G>A (p.Asp812Asn) rs1193165605 0.00001
NM_004519.4(KCNQ3):c.2534T>C (p.Phe845Ser) rs751186425 0.00001
NM_004519.4(KCNQ3):c.2537C>T (p.Thr846Met) rs765623435 0.00001
NM_004519.4(KCNQ3):c.2545G>A (p.Gly849Ser) rs761201259 0.00001
NM_004519.4(KCNQ3):c.2567C>T (p.Thr856Ile) rs762078830 0.00001
NM_004519.4(KCNQ3):c.2587T>G (p.Ser863Ala) rs1824773305 0.00001
NM_004519.4(KCNQ3):c.293A>G (p.Lys98Arg) rs143194379 0.00001
NM_004519.4(KCNQ3):c.659A>G (p.Asn220Ser) rs1826713495 0.00001
NM_004519.4(KCNQ3):c.91G>A (p.Gly31Arg) rs1433483426 0.00001
NM_004519.4(KCNQ3):c.-6A>G rs780717504
NM_004519.4(KCNQ3):c.1016T>C (p.Ile339Thr)
NM_004519.4(KCNQ3):c.1028T>C (p.Phe343Ser) rs2130128090
NM_004519.4(KCNQ3):c.1040C>T (p.Pro347Leu) rs2130128031
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.1120C>T (p.Pro374Ser)
NM_004519.4(KCNQ3):c.1132C>G (p.Leu378Val) rs2130121043
NM_004519.4(KCNQ3):c.1157A>C (p.Tyr386Ser)
NM_004519.4(KCNQ3):c.1169C>T (p.Pro390Leu)
NM_004519.4(KCNQ3):c.1190C>T (p.Ala397Val)
NM_004519.4(KCNQ3):c.1216G>T (p.Val406Phe)
NM_004519.4(KCNQ3):c.1249_1250delinsAT (p.Glu417Met) rs1554625699
NM_004519.4(KCNQ3):c.1280T>C (p.Leu427Ser) rs1825289329
NM_004519.4(KCNQ3):c.1291C>T (p.Arg431Cys)
NM_004519.4(KCNQ3):c.1292G>A (p.Arg431His) rs2130944718
NM_004519.4(KCNQ3):c.1330C>G (p.Leu444Val)
NM_004519.4(KCNQ3):c.1339C>A (p.Pro447Thr) rs759734514
NM_004519.4(KCNQ3):c.1468G>A (p.Ala490Thr)
NM_004519.4(KCNQ3):c.1490C>A (p.Ala497Glu) rs1048969639
NM_004519.4(KCNQ3):c.1531A>G (p.Met511Val) rs200219106
NM_004519.4(KCNQ3):c.1567A>G (p.Arg523Gly) rs2130942238
NM_004519.4(KCNQ3):c.1591A>G (p.Lys531Glu) rs796052681
NM_004519.4(KCNQ3):c.1599dup (p.Phe534fs) rs762289015
NM_004519.4(KCNQ3):c.1621del (p.Tyr541fs) rs2130938733
NM_004519.4(KCNQ3):c.1625A>G (p.Asp542Gly) rs2130938716
NM_004519.4(KCNQ3):c.1644G>T (p.Glu548Asp) rs775965122
NM_004519.4(KCNQ3):c.1694A>G (p.Gln565Arg) rs1003860988
NM_004519.4(KCNQ3):c.169C>G (p.Leu57Val)
NM_004519.4(KCNQ3):c.1715dup (p.Thr573fs) rs796052684
NM_004519.4(KCNQ3):c.1720C>A (p.Pro574Thr) rs74582884
NM_004519.4(KCNQ3):c.1721C>G (p.Pro574Arg) rs2130931673
NM_004519.4(KCNQ3):c.1727C>G (p.Pro576Arg) rs371890934
NM_004519.4(KCNQ3):c.173G>T (p.Gly58Val) rs1822520136
NM_004519.4(KCNQ3):c.1780C>T (p.Pro594Ser) rs868191966
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>T (p.Val629Phe) rs185511111
NM_004519.4(KCNQ3):c.2004A>C (p.Glu668Asp)
NM_004519.4(KCNQ3):c.2011AAG[1] (p.Lys672del) rs777822578
NM_004519.4(KCNQ3):c.2035G>A (p.Asp679Asn) rs773672399
NM_004519.4(KCNQ3):c.2060A>G (p.Tyr687Cys)
NM_004519.4(KCNQ3):c.2072G>A (p.Gly691Asp) rs758790946
NM_004519.4(KCNQ3):c.2074C>G (p.Pro692Ala) rs1131691408
NM_004519.4(KCNQ3):c.2093G>A (p.Ser698Asn) rs1824804011
NM_004519.4(KCNQ3):c.212G>A (p.Gly71Asp)
NM_004519.4(KCNQ3):c.2149C>T (p.Pro717Ser)
NM_004519.4(KCNQ3):c.2187G>T (p.Lys729Asn)
NM_004519.4(KCNQ3):c.2194G>A (p.Ala732Thr) rs796052682
NM_004519.4(KCNQ3):c.2225T>G (p.Val742Gly) rs1057517883
NM_004519.4(KCNQ3):c.2257C>A (p.Leu753Ile)
NM_004519.4(KCNQ3):c.2317C>T (p.Arg773Ter)
NM_004519.4(KCNQ3):c.2330G>T (p.Arg777Leu)
NM_004519.4(KCNQ3):c.2357G>C (p.Ser786Thr) rs2130923041
NM_004519.4(KCNQ3):c.2446T>C (p.Tyr816His)
NM_004519.4(KCNQ3):c.2458C>A (p.Pro820Thr)
NM_004519.4(KCNQ3):c.2469dup (p.Ser824fs) rs886041208
NM_004519.4(KCNQ3):c.2611C>G (p.Pro871Ala) rs200647826
NM_004519.4(KCNQ3):c.330G>C (p.Leu110Phe) rs796052673
NM_004519.4(KCNQ3):c.361T>G (p.Trp121Gly)
NM_004519.4(KCNQ3):c.36_60del (p.Gly13fs) rs772417096
NM_004519.4(KCNQ3):c.402G>A (p.Leu134=) rs1253481641
NM_004519.4(KCNQ3):c.40G>A (p.Gly14Ser) rs1357758074
NM_004519.4(KCNQ3):c.477+5G>A rs373813381
NM_004519.4(KCNQ3):c.50_58dup (p.Asp17_Gly19dup) rs1281937576
NM_004519.4(KCNQ3):c.50_61del (p.Asp17_Gly20del) rs1186895673
NM_004519.4(KCNQ3):c.569G>A (p.Arg190Gln) rs796052674
NM_004519.4(KCNQ3):c.56_73del (p.Gly19_Gly24del) rs774616642
NM_004519.4(KCNQ3):c.588G>T (p.Lys196Asn)
NM_004519.4(KCNQ3):c.63_71dup (p.Gly22_Gly24dup) rs748459358
NM_004519.4(KCNQ3):c.697C>A (p.Gln233Lys)
NM_004519.4(KCNQ3):c.725G>A (p.Arg242Gln) rs1826708929
NM_004519.4(KCNQ3):c.737C>T (p.Thr246Ile)
NM_004519.4(KCNQ3):c.781C>T (p.Leu261Phe) rs2130134314
NM_004519.4(KCNQ3):c.80A>G (p.Asn27Ser) rs1342457621
NM_004519.4(KCNQ3):c.924G>A (p.Trp308Ter) rs1554627423
NM_004519.4(KCNQ3):c.962A>G (p.Asp321Gly)
NM_004519.4(KCNQ3):c.977C>T (p.Thr326Met) rs1326172406

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