ClinVar Miner

List of variants in gene KCNQ3 reported as likely benign for not specified

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.1071C>G (p.Leu357=) rs17575754 0.05655
NM_004519.4(KCNQ3):c.732T>C (p.Gly244=) rs41272387 0.05313
NM_004519.4(KCNQ3):c.660T>C (p.Asn220=) rs41272389 0.05312
NM_004519.4(KCNQ3):c.1241A>G (p.Glu414Gly) rs2303995 0.02242
NM_004519.4(KCNQ3):c.1059C>T (p.Ser353=) rs35413925 0.01009
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=) rs35538317 0.00761
NM_004519.4(KCNQ3):c.948C>T (p.Thr316=) rs142144538 0.00564
NM_004519.4(KCNQ3):c.225C>G (p.Asp75Glu) rs138254004 0.00029
NM_004519.4(KCNQ3):c.933+12C>T rs113965977 0.00010
NM_004519.4(KCNQ3):c.168G>C (p.Ala56=) rs777374664 0.00009
NM_004519.4(KCNQ3):c.478-15T>C rs1057520808 0.00008
NM_004519.4(KCNQ3):c.*9A>G rs1057523827 0.00003
NM_004519.4(KCNQ3):c.1119G>A (p.Lys373=) rs148581537 0.00003
NM_004519.4(KCNQ3):c.2388C>T (p.Asn796=) rs957388952 0.00003
NM_004519.4(KCNQ3):c.99G>A (p.Ala33=) rs1057520485 0.00003
NM_004519.4(KCNQ3):c.-13G>C rs796052671 0.00002
NM_004519.4(KCNQ3):c.1800-10T>C rs774538909 0.00002
NM_004519.4(KCNQ3):c.386+15G>T rs778486411 0.00002
NM_004519.4(KCNQ3):c.1005C>A (p.Thr335=) rs758511572 0.00001
NM_004519.4(KCNQ3):c.1045-4C>T rs777650536 0.00001
NM_004519.4(KCNQ3):c.1700+12A>C rs1035669898 0.00001
NM_004519.4(KCNQ3):c.1799+17T>C rs772154355 0.00001
NM_004519.4(KCNQ3):c.1800-12G>A rs761923188 0.00001
NM_004519.4(KCNQ3):c.1800-13C>T rs772137862 0.00001
NM_004519.4(KCNQ3):c.2034C>T (p.Ser678=) rs560675018 0.00001
NM_004519.4(KCNQ3):c.2451G>T (p.Val817=) rs754874948 0.00001
NM_004519.4(KCNQ3):c.2562G>A (p.Ser854=) rs201736771 0.00001
NM_004519.4(KCNQ3):c.35C>T (p.Ala12Val) rs796052672 0.00001
NM_004519.4(KCNQ3):c.478-20C>T rs543697742 0.00001
NM_004519.4(KCNQ3):c.604+10G>T rs541587196 0.00001
NM_004519.4(KCNQ3):c.624C>T (p.Ala208=) rs747188490 0.00001
NM_004519.4(KCNQ3):c.789G>A (p.Thr263=) rs762086066 0.00001
NM_004519.4(KCNQ3):c.81C>T (p.Asn27=) rs1271630840 0.00001
NM_004519.4(KCNQ3):c.891A>G (p.Lys297=) rs757426539 0.00001
NM_004519.4(KCNQ3):c.897G>A (p.Glu299=) rs367611806 0.00001
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.1470C>G (p.Ala490=) rs765705898
NM_004519.4(KCNQ3):c.1569-11T>A rs1057520865
NM_004519.4(KCNQ3):c.1638G>A (p.Val546=) rs765209359
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1799+6G>A rs1554622021
NM_004519.4(KCNQ3):c.1839C>T (p.Ile613=) rs140045642
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.387-12C>A rs773400738
NM_004519.4(KCNQ3):c.429C>T (p.Thr143=) rs1257391946
NM_004519.4(KCNQ3):c.478-16A>T rs781487724
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.57C>A (p.Gly19=) rs1057522486
NM_004519.4(KCNQ3):c.604+16G>A rs1554628744
NM_004519.4(KCNQ3):c.609C>T (p.Ile203=) rs574174380
NM_004519.4(KCNQ3):c.75G>C (p.Ala25=) rs1554660829

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