ClinVar Miner

List of variants in gene KCNQ3 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.*4817G>A rs76758430 0.00586
NM_004519.4(KCNQ3):c.*4949G>T rs561176499 0.00201
NM_004519.4(KCNQ3):c.*5965T>C rs537622929 0.00150
NM_004519.4(KCNQ3):c.1917C>T (p.Leu639=) rs78731303 0.00131
NM_004519.4(KCNQ3):c.*3591T>C rs778136645 0.00130
NM_004519.4(KCNQ3):c.*4456A>C rs533328133 0.00104
NM_004519.4(KCNQ3):c.*6831G>A rs529301177 0.00078
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831 0.00043
NM_004519.4(KCNQ3):c.*2010T>A rs139631143 0.00037
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246 0.00031
NM_004519.4(KCNQ3):c.*5971C>A rs749511015 0.00024
NM_004519.4(KCNQ3):c.*5391C>T rs569024726 0.00021
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254 0.00021
NM_004519.4(KCNQ3):c.1964C>T (p.Thr655Met) rs199942237 0.00019
NM_004519.4(KCNQ3):c.1391T>C (p.Val464Ala) rs143664009 0.00018
NM_004519.4(KCNQ3):c.1885G>C (p.Val629Leu) rs185511111 0.00016
NM_004519.4(KCNQ3):c.2237C>T (p.Thr746Met) rs375833070 0.00009
NM_004519.4(KCNQ3):c.1935A>G (p.Gln645=) rs587781011 0.00008
NM_004519.4(KCNQ3):c.2144A>G (p.His715Arg) rs112314858 0.00007
NM_004519.4(KCNQ3):c.2338C>T (p.Arg780Cys) rs138852641 0.00007
NM_004519.4(KCNQ3):c.2614A>G (p.Ile872Val) rs199682667 0.00006
NM_004519.4(KCNQ3):c.1995G>A (p.Ser665=) rs759776061 0.00005
NM_004519.4(KCNQ3):c.1563C>T (p.Ala521=) rs186310292 0.00004
NM_004519.4(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496 0.00004
NM_004519.4(KCNQ3):c.2312C>T (p.Ser771Leu) rs372002816 0.00004
NM_004519.4(KCNQ3):c.1178T>C (p.Ile393Thr) rs201814804 0.00003
NM_004519.4(KCNQ3):c.2388C>T (p.Asn796=) rs957388952 0.00003
NM_004519.4(KCNQ3):c.855C>T (p.Asp285=) rs62519577 0.00003
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988 0.00002
NM_004519.4(KCNQ3):c.1698G>A (p.Thr566=) rs781066375 0.00001
NM_004519.4(KCNQ3):c.1709T>C (p.Met570Thr) rs199999939 0.00001
NM_004519.4(KCNQ3):c.1918G>A (p.Val640Met) rs767903815 0.00001
NM_004519.4(KCNQ3):c.1945C>T (p.Arg649Trp) rs770863845 0.00001
NM_004519.4(KCNQ3):c.2086C>A (p.Pro696Thr) rs1055327554 0.00001
NM_004519.4(KCNQ3):c.2123G>T (p.Ser708Ile) rs977989588 0.00001
NM_004519.4(KCNQ3):c.2146G>C (p.Asp716His) rs149324120 0.00001
NM_004519.4(KCNQ3):c.2472G>C (p.Ser824=) rs774287489 0.00001
NM_004519.4(KCNQ3):c.2502C>T (p.Ala834=) rs1248992112 0.00001
NM_004519.4(KCNQ3):c.897G>A (p.Glu299=) rs367611806 0.00001
NM_004519.4(KCNQ3):c.*2007_*2009dup
NM_004519.4(KCNQ3):c.*6046G>A rs565715084
NM_004519.4(KCNQ3):c.-148_-147insTG rs886062698
NM_004519.4(KCNQ3):c.101C>A (p.Ala34Glu) rs1412895282
NM_004519.4(KCNQ3):c.1252G>A (p.Ala418Thr)
NM_004519.4(KCNQ3):c.1465+7C>G
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1921G>A (p.Asp641Asn)
NM_004519.4(KCNQ3):c.194G>C (p.Gly65Ala) rs1822519573
NM_004519.4(KCNQ3):c.1958A>G (p.Gln653Arg) rs554833870
NM_004519.4(KCNQ3):c.216C>T (p.Gly72=)
NM_004519.4(KCNQ3):c.2193G>A (p.Gln731=)
NM_004519.4(KCNQ3):c.231G>A (p.Gly77=) rs1195159317
NM_004519.4(KCNQ3):c.386+32938C>T rs552538402
NM_004519.4(KCNQ3):c.387-1035C>T
NM_004519.4(KCNQ3):c.689G>A (p.Arg230His)
NM_004519.4(KCNQ3):c.933G>A (p.Leu311=) rs2130133290
NM_004519.4(KCNQ3):c.938C>T (p.Thr313Ile) rs1826478037
NM_004519.4(KCNQ3):c.956A>G (p.Tyr319Cys) rs1554627218
NM_004519.4(KCNQ3):c.989G>A (p.Arg330His) rs1162306056
NM_004519.4(KCNQ3):c.997G>C (p.Ala333Pro) rs1064797349

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