ClinVar Miner

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

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Total variants: 18
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HGVS dbSNP
NM_004519.4(KCNQ3):c.1216G>A (p.Val406Ile) rs144474368
NM_004519.4(KCNQ3):c.1249_1250delinsAT (p.Glu417Met) rs1554625699
NM_004519.4(KCNQ3):c.1531A>G (p.Met511Val) rs200219106
NM_004519.4(KCNQ3):c.1552G>A (p.Ala518Thr) rs745463637
NM_004519.4(KCNQ3):c.1562C>G (p.Ala521Gly) rs1057518505
NM_004519.4(KCNQ3):c.1617G>C (p.Arg539Ser) rs140607300
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111
NM_004519.4(KCNQ3):c.1995G>A (p.Ser665=) rs759776061
NM_004519.4(KCNQ3):c.2225T>G (p.Val742Gly) rs1057517883
NM_004519.4(KCNQ3):c.2237C>T (p.Thr746Met) rs375833070
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2491C>T (p.Arg831Trp) rs185628977
NM_004519.4(KCNQ3):c.2492G>A (p.Arg831Gln) rs149004528
NM_004519.4(KCNQ3):c.2567C>T (p.Thr856Ile) rs762078830
NM_004519.4(KCNQ3):c.2611C>G (p.Pro871Ala) rs200647826
NM_004519.4(KCNQ3):c.36_60del (p.Gly13fs) rs772417096
NM_004519.4(KCNQ3):c.56_73del (p.Gly19_Gly24del) rs774616642
NM_004519.4(KCNQ3):c.63_71dup (p.Gly22_Gly24dup) rs748459358

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