ClinVar Miner

List of variants in gene KCNQ3 reported as likely benign by Invitae

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Total variants: 27
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HGVS dbSNP
NM_001204824.1(KCNQ3):c.1970G>A (p.Arg657Gln) rs201328910
NM_001204824.1(KCNQ3):c.717G>A (p.Val239=) rs750375617
NM_004519.3(KCNQ3):c.1044+7A>G rs1437816175
NM_004519.3(KCNQ3):c.1045-4C>T rs777650536
NM_004519.3(KCNQ3):c.1209A>G (p.Glu403=) rs1554626530
NM_004519.3(KCNQ3):c.1215C>T (p.Val405=) rs370250223
NM_004519.3(KCNQ3):c.1248G>A (p.Leu416=) rs913811509
NM_004519.3(KCNQ3):c.12G>A (p.Lys4=) rs1554660855
NM_004519.3(KCNQ3):c.141C>T (p.Pro47=) rs563366275
NM_004519.3(KCNQ3):c.1548G>A (p.Lys516=) rs994157818
NM_004519.3(KCNQ3):c.1549G>A (p.Ala517Thr) rs1554622834
NM_004519.3(KCNQ3):c.1617G>A (p.Arg539=) rs140607300
NM_004519.3(KCNQ3):c.1677C>A (p.Ser559=) rs377613824
NM_004519.3(KCNQ3):c.1701-4T>C rs1060503978
NM_004519.3(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.3(KCNQ3):c.183C>G (p.Ala61=) rs761977947
NM_004519.3(KCNQ3):c.1986C>A (p.Gly662=) rs140383266
NM_004519.3(KCNQ3):c.2079G>A (p.Pro693=) rs145204452
NM_004519.3(KCNQ3):c.2123G>T (p.Ser708Ile) rs977989588
NM_004519.3(KCNQ3):c.2129A>G (p.Tyr710Cys) rs1060500605
NM_004519.3(KCNQ3):c.2133G>A (p.Gly711=) rs199701721
NM_004519.3(KCNQ3):c.2298G>C (p.Leu766=) rs752643910
NM_004519.3(KCNQ3):c.2343C>T (p.Ser781=) rs200772304
NM_004519.3(KCNQ3):c.2391C>T (p.His797=) rs763446963
NM_004519.3(KCNQ3):c.2619A>G (p.Ter873=) rs893752295
NM_004519.3(KCNQ3):c.39C>T (p.Gly13=) rs1313781213
NM_004519.3(KCNQ3):c.679C>A (p.Arg227=) rs796052675

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