ClinVar Miner

List of variants in gene KCNQ3 reported as benign

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Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP
GRCh37/hg19 8q24.22(chr8:133226397-133306801)x1
NM_004519.4(KCNQ3):c.*1050A>C rs76720699
NM_004519.4(KCNQ3):c.*1407A>C rs76570743
NM_004519.4(KCNQ3):c.*1754C>T rs977939
NM_004519.4(KCNQ3):c.*2137C>T rs2272679
NM_004519.4(KCNQ3):c.*2475C>T rs141143602
NM_004519.4(KCNQ3):c.*3032A>G rs2469626
NM_004519.4(KCNQ3):c.*3035A>G rs2469627
NM_004519.4(KCNQ3):c.*3597G>A rs1025436
NM_004519.4(KCNQ3):c.*396A>G rs78243592
NM_004519.4(KCNQ3):c.*3977G>A rs2469628
NM_004519.4(KCNQ3):c.*4125T>C rs2163608
NM_004519.4(KCNQ3):c.*4243A>T rs2436131
NM_004519.4(KCNQ3):c.*425C>A rs10956641
NM_004519.4(KCNQ3):c.*426C>G rs10956640
NM_004519.4(KCNQ3):c.*4746_*4747insACAG rs112550767
NM_004519.4(KCNQ3):c.*4958A>G rs1437824
NM_004519.4(KCNQ3):c.*4982A>T rs545252668
NM_004519.4(KCNQ3):c.*4982del rs35772668
NM_004519.4(KCNQ3):c.*5719C>T rs11786417
NM_004519.4(KCNQ3):c.*5932A>C rs2436130
NM_004519.4(KCNQ3):c.*6238T>C rs10108362
NM_004519.4(KCNQ3):c.*6282A>T rs10095295
NM_004519.4(KCNQ3):c.*6340G>A rs2469629
NM_004519.4(KCNQ3):c.*6632T>C rs9297840
NM_004519.4(KCNQ3):c.*6812A>G rs7815106
NM_004519.4(KCNQ3):c.*6874C>G rs2436129
NM_004519.4(KCNQ3):c.*6956A>G rs2469630
NM_004519.4(KCNQ3):c.*7033T>C rs2436128
NM_004519.4(KCNQ3):c.*7075A>G rs2436127
NM_004519.4(KCNQ3):c.*7095T>G rs1437823
NM_004519.4(KCNQ3):c.*7119C>T rs2436126
NM_004519.4(KCNQ3):c.*7131G>A rs75865310
NM_004519.4(KCNQ3):c.*7143A>G rs2436125
NM_004519.4(KCNQ3):c.*717_*718CA[18] rs35230760
NM_004519.4(KCNQ3):c.*7221C>T rs2436124
NM_004519.4(KCNQ3):c.*7371T>G rs76268875
NM_004519.4(KCNQ3):c.*7506C>T rs11785257
NM_004519.4(KCNQ3):c.*8148G>A rs1437822
NM_004519.4(KCNQ3):c.-142G>T rs28606540
NM_004519.4(KCNQ3):c.-318G>A
NM_004519.4(KCNQ3):c.-504A>G
NM_004519.4(KCNQ3):c.-519C>G
NM_004519.4(KCNQ3):c.-556T>G
NM_004519.4(KCNQ3):c.-7G>C rs745345051
NM_004519.4(KCNQ3):c.1044+156A>G
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.1235+38A>G
NM_004519.4(KCNQ3):c.1236-134C>T
NM_004519.4(KCNQ3):c.1236-16C>T rs201168632
NM_004519.4(KCNQ3):c.1236-64C>T
NM_004519.4(KCNQ3):c.1241A>G (p.Glu414Gly) rs2303995
NM_004519.4(KCNQ3):c.1262+269T>C
NM_004519.4(KCNQ3):c.1465+256A>G
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=) rs35538317
NM_004519.4(KCNQ3):c.1568+12A>G rs181790623
NM_004519.4(KCNQ3):c.1568+14G>A rs370848714
NM_004519.4(KCNQ3):c.1626T>C (p.Asp542=) rs145098530
NM_004519.4(KCNQ3):c.1700+29G>A
NM_004519.4(KCNQ3):c.1700+3G>A rs115092422
NM_004519.4(KCNQ3):c.1701-17C>T rs375928058
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1885-110C>T
NM_004519.4(KCNQ3):c.1885-67C>G
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.1994C>T (p.Ser665Leu) rs147173555
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.2306C>A (p.Pro769His) rs114095081
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831
NM_004519.4(KCNQ3):c.240G>A (p.Arg80=) rs587781012
NM_004519.4(KCNQ3):c.386+32845T>C
NM_004519.4(KCNQ3):c.605-302C>T
NM_004519.4(KCNQ3):c.660T>C (p.Asn220=) rs41272389
NM_004519.4(KCNQ3):c.732T>C (p.Gly244=) rs41272387
NM_004519.4(KCNQ3):c.777+121C>T
NM_004519.4(KCNQ3):c.777+135A>G
NM_004519.4(KCNQ3):c.777+220G>C
NM_004519.4(KCNQ3):c.777+225G>C
NM_004519.4(KCNQ3):c.777+306G>C
NM_004519.4(KCNQ3):c.778-17A>C rs373349894
NM_004519.4(KCNQ3):c.778-203T>G
NM_004519.4(KCNQ3):c.834T>C (p.Leu278=) rs769657433
NM_004519.4(KCNQ3):c.933+114G>A
NM_004519.4(KCNQ3):c.933+128A>T
NM_004519.4(KCNQ3):c.933+129A>C
NM_004519.4(KCNQ3):c.933+25T>C
NM_004519.4(KCNQ3):c.934-108G>A
NM_004519.4(KCNQ3):c.934-228C>T
NM_004519.4(KCNQ3):c.948C>T (p.Thr316=) rs142144538
NM_004519.4(KCNQ3):c.954C>A (p.Gly318=) rs143224896

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