ClinVar Miner

List of variants in gene KCNQ3 studied for not specified

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Gene type:
ClinVar version:
Total variants: 104
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HGVS dbSNP
NM_004519.3(KCNQ3):c.1885-5dupT rs769845388
NM_004519.4(KCNQ3):c.*9A>G rs1057523827
NM_004519.4(KCNQ3):c.-13G>C rs796052671
NM_004519.4(KCNQ3):c.-7G>C rs745345051
NM_004519.4(KCNQ3):c.1005C>A (p.Thr335=) rs758511572
NM_004519.4(KCNQ3):c.1026C>T (p.Ser342=) rs1057524036
NM_004519.4(KCNQ3):c.1032T>C (p.Phe344=) rs1554627208
NM_004519.4(KCNQ3):c.1045-4C>T rs777650536
NM_004519.4(KCNQ3):c.1059C>T (p.Ser353=) rs35413925
NM_004519.4(KCNQ3):c.1071C>G (p.Leu357=) rs17575754
NM_004519.4(KCNQ3):c.1119G>A (p.Lys373=) rs148581537
NM_004519.4(KCNQ3):c.1141-3C>T rs377479583
NM_004519.4(KCNQ3):c.1216G>A (p.Val406Ile) rs144474368
NM_004519.4(KCNQ3):c.1236-16C>T rs201168632
NM_004519.4(KCNQ3):c.1241A>G (p.Glu414Gly) rs2303995
NM_004519.4(KCNQ3):c.1249_1250delinsAT (p.Glu417Met) rs1554625699
NM_004519.4(KCNQ3):c.1391T>C (p.Val464Ala) rs143664009
NM_004519.4(KCNQ3):c.1470C>G (p.Ala490=) rs765705898
NM_004519.4(KCNQ3):c.1531A>G (p.Met511Val) rs200219106
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=) rs35538317
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.1563C>T (p.Ala521=) rs186310292
NM_004519.4(KCNQ3):c.1568+12A>G rs181790623
NM_004519.4(KCNQ3):c.1568+14G>A rs370848714
NM_004519.4(KCNQ3):c.1569-11T>A rs1057520865
NM_004519.4(KCNQ3):c.1617G>C (p.Arg539Ser) rs140607300
NM_004519.4(KCNQ3):c.1623C>T (p.Tyr541=) rs138900075
NM_004519.4(KCNQ3):c.1626T>C (p.Asp542=) rs145098530
NM_004519.4(KCNQ3):c.1638G>A (p.Val546=) rs765209359
NM_004519.4(KCNQ3):c.1677C>A (p.Ser559=) rs377613824
NM_004519.4(KCNQ3):c.168G>C (p.Ala56=) rs777374664
NM_004519.4(KCNQ3):c.1700+12A>C rs1035669898
NM_004519.4(KCNQ3):c.1701-17C>T rs375928058
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1799+17T>C rs772154355
NM_004519.4(KCNQ3):c.1799+6G>A rs1554622021
NM_004519.4(KCNQ3):c.1800-10T>C rs774538909
NM_004519.4(KCNQ3):c.1800-12G>A rs761923188
NM_004519.4(KCNQ3):c.1800-13C>T rs772137862
NM_004519.4(KCNQ3):c.1839C>T (p.Ile613=) rs140045642
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111
NM_004519.4(KCNQ3):c.1917C>T (p.Leu639=) rs78731303
NM_004519.4(KCNQ3):c.1935A>G (p.Gln645=) rs587781011
NM_004519.4(KCNQ3):c.1947G>A (p.Arg649=) rs142082768
NM_004519.4(KCNQ3):c.1958A>G (p.Gln653Arg) rs554833870
NM_004519.4(KCNQ3):c.1964C>T (p.Thr655Met) rs199942237
NM_004519.4(KCNQ3):c.1994C>T (p.Ser665Leu) rs147173555
NM_004519.4(KCNQ3):c.1995G>A (p.Ser665=) rs759776061
NM_004519.4(KCNQ3):c.2034C>T (p.Ser678=) rs560675018
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988
NM_004519.4(KCNQ3):c.2079G>A (p.Pro693=) rs145204452
NM_004519.4(KCNQ3):c.2097C>T (p.Phe699=) rs139678098
NM_004519.4(KCNQ3):c.2168G>A (p.Gly723Glu) rs142149782
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.225C>G (p.Asp75Glu) rs138254004
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His) rs114095081
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831
NM_004519.4(KCNQ3):c.2388C>T (p.Asn796=) rs957388952
NM_004519.4(KCNQ3):c.240G>A (p.Arg80=) rs587781012
NM_004519.4(KCNQ3):c.2451G>T (p.Val817=) rs754874948
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254
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.2538G>A (p.Thr846=) rs541215515
NM_004519.4(KCNQ3):c.2550C>T (p.Ser850=) rs1554621294
NM_004519.4(KCNQ3):c.2556T>G (p.Pro852=) rs763432119
NM_004519.4(KCNQ3):c.2562G>A (p.Ser854=) rs201736771
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.35C>T (p.Ala12Val) rs796052672
NM_004519.4(KCNQ3):c.36_60del (p.Gly13fs) rs772417096
NM_004519.4(KCNQ3):c.386+15G>T rs778486411
NM_004519.4(KCNQ3):c.387-12C>A rs773400738
NM_004519.4(KCNQ3):c.429C>T (p.Thr143=) rs1257391946
NM_004519.4(KCNQ3):c.478-15T>C rs1057520808
NM_004519.4(KCNQ3):c.478-16A>T rs781487724
NM_004519.4(KCNQ3):c.478-20C>T rs543697742
NM_004519.4(KCNQ3):c.507C>T (p.Ala169=) rs1220196153
NM_004519.4(KCNQ3):c.567C>T (p.Gly189=) rs1057524531
NM_004519.4(KCNQ3):c.56_73del (p.Gly19_Gly24del) rs774616642
NM_004519.4(KCNQ3):c.57C>A (p.Gly19=) rs1057522486
NM_004519.4(KCNQ3):c.604+10G>T rs541587196
NM_004519.4(KCNQ3):c.604+16G>A rs1554628744
NM_004519.4(KCNQ3):c.609C>T (p.Ile203=) rs574174380
NM_004519.4(KCNQ3):c.624C>T (p.Ala208=) rs747188490
NM_004519.4(KCNQ3):c.63_71dup (p.Gly22_Gly24dup) rs748459358
NM_004519.4(KCNQ3):c.660T>C (p.Asn220=) rs41272389
NM_004519.4(KCNQ3):c.714G>A (p.Leu238=) rs377171734
NM_004519.4(KCNQ3):c.732T>C (p.Gly244=) rs41272387
NM_004519.4(KCNQ3):c.75G>C (p.Ala25=) rs1554660829
NM_004519.4(KCNQ3):c.778-17A>C rs373349894
NM_004519.4(KCNQ3):c.789G>A (p.Thr263=) rs762086066
NM_004519.4(KCNQ3):c.81C>T (p.Asn27=) rs1271630840
NM_004519.4(KCNQ3):c.834T>C (p.Leu278=) rs769657433
NM_004519.4(KCNQ3):c.891A>G (p.Lys297=) rs757426539
NM_004519.4(KCNQ3):c.897G>A (p.Glu299=) rs367611806
NM_004519.4(KCNQ3):c.933+12C>T rs113965977
NM_004519.4(KCNQ3):c.948C>T (p.Thr316=) rs142144538
NM_004519.4(KCNQ3):c.954C>A (p.Gly318=) rs143224896
NM_004519.4(KCNQ3):c.99G>A (p.Ala33=) rs1057520485

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