ClinVar Miner

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

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Gene type:
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Total variants: 70
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HGVS dbSNP
NM_004519.4(KCNQ3):c.1020C>T (p.Gly340=) rs1490473853
NM_004519.4(KCNQ3):c.102G>A (p.Ala34=) rs1587060440
NM_004519.4(KCNQ3):c.1044+7A>G rs1437816175
NM_004519.4(KCNQ3):c.1045-4C>T rs777650536
NM_004519.4(KCNQ3):c.1077G>A (p.Val359=) rs750375617
NM_004519.4(KCNQ3):c.1209A>G (p.Glu403=) rs1554626530
NM_004519.4(KCNQ3):c.1215C>T (p.Val405=) rs370250223
NM_004519.4(KCNQ3):c.1236-4C>T rs768705754
NM_004519.4(KCNQ3):c.1248G>A (p.Leu416=) rs913811509
NM_004519.4(KCNQ3):c.12G>A (p.Lys4=) rs1554660855
NM_004519.4(KCNQ3):c.138G>T (p.Ala46=) rs745755804
NM_004519.4(KCNQ3):c.1403A>G (p.Asn468Ser) rs118192252
NM_004519.4(KCNQ3):c.1410G>A (p.Glu470=) rs1586763916
NM_004519.4(KCNQ3):c.141C>T (p.Pro47=) rs563366275
NM_004519.4(KCNQ3):c.1466-6T>C rs1586762811
NM_004519.4(KCNQ3):c.1491G>A (p.Ala497=) rs760918194
NM_004519.4(KCNQ3):c.1548G>A (p.Lys516=) rs994157818
NM_004519.4(KCNQ3):c.1549G>A (p.Ala517Thr) rs1554622834
NM_004519.4(KCNQ3):c.1611T>C (p.Thr537=) rs1586760577
NM_004519.4(KCNQ3):c.1617G>A (p.Arg539=) rs140607300
NM_004519.4(KCNQ3):c.1623C>T (p.Tyr541=) rs138900075
NM_004519.4(KCNQ3):c.1656C>T (p.Ala552=) rs199722269
NM_004519.4(KCNQ3):c.1677C>A (p.Ser559=) rs377613824
NM_004519.4(KCNQ3):c.1701-4T>C rs1060503978
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1800-10T>C rs774538909
NM_004519.4(KCNQ3):c.1812T>C (p.Tyr604=) rs749500398
NM_004519.4(KCNQ3):c.183C>G (p.Ala61=) rs761977947
NM_004519.4(KCNQ3):c.1947G>A (p.Arg649=) rs142082768
NM_004519.4(KCNQ3):c.1986C>A (p.Gly662=) rs140383266
NM_004519.4(KCNQ3):c.1995G>A (p.Ser665=) rs759776061
NM_004519.4(KCNQ3):c.1998A>G (p.Pro666=) rs1586750955
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988
NM_004519.4(KCNQ3):c.2076C>A (p.Pro692=) rs765395005
NM_004519.4(KCNQ3):c.2079G>A (p.Pro693=) rs145204452
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.2129A>G (p.Tyr710Cys) rs1060500605
NM_004519.4(KCNQ3):c.2133G>A (p.Gly711=) rs199701721
NM_004519.4(KCNQ3):c.2238G>A (p.Thr746=) rs769350034
NM_004519.4(KCNQ3):c.225C>G (p.Asp75Glu) rs138254004
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246
NM_004519.4(KCNQ3):c.2298G>C (p.Leu766=) rs752643910
NM_004519.4(KCNQ3):c.231G>A (p.Gly77=) rs1195159317
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2343C>T (p.Ser781=) rs200772304
NM_004519.4(KCNQ3):c.2391C>T (p.His797=) rs763446963
NM_004519.4(KCNQ3):c.2442T>C (p.Asp814=) rs758166616
NM_004519.4(KCNQ3):c.2472G>A (p.Ser824=) rs774287489
NM_004519.4(KCNQ3):c.2491C>T (p.Arg831Trp) rs185628977
NM_004519.4(KCNQ3):c.2499C>T (p.Leu833=) rs773301064
NM_004519.4(KCNQ3):c.2514G>A (p.Thr838=) rs568466967
NM_004519.4(KCNQ3):c.2514G>C (p.Thr838=) rs568466967
NM_004519.4(KCNQ3):c.2520A>G (p.Thr840=) rs780185117
NM_004519.4(KCNQ3):c.2538G>A (p.Thr846=) rs541215515
NM_004519.4(KCNQ3):c.2544C>T (p.Ser848=) rs766822002
NM_004519.4(KCNQ3):c.2619A>G (p.Ter873=) rs893752295
NM_004519.4(KCNQ3):c.39C>T (p.Gly13=) rs1313781213
NM_004519.4(KCNQ3):c.429C>A (p.Thr143=) rs1257391946
NM_004519.4(KCNQ3):c.477+7T>C rs757078055
NM_004519.4(KCNQ3):c.562C>A (p.Arg188=) rs754551218
NM_004519.4(KCNQ3):c.676C>T (p.Leu226=) rs1586806127
NM_004519.4(KCNQ3):c.679C>A (p.Arg227=) rs796052675
NM_004519.4(KCNQ3):c.690C>T (p.Arg230=) rs779577320
NM_004519.4(KCNQ3):c.723C>T (p.Asp241=) rs1586806052
NM_004519.4(KCNQ3):c.778-10A>G rs750579086
NM_004519.4(KCNQ3):c.81C>T (p.Asn27=) rs1271630840
NM_004519.4(KCNQ3):c.855C>T (p.Asp285=) rs62519577
NM_004519.4(KCNQ3):c.897G>A (p.Glu299=) rs367611806
NM_004519.4(KCNQ3):c.99G>A (p.Ala33=) rs1057520485

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