ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.*5965T>C rs537622929 0.00150
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.2263G>A (p.Asp755Asn) rs150821246 0.00031
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.1935A>G (p.Gln645=) rs587781011 0.00008
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.2312C>T (p.Ser771Leu) rs372002816 0.00004
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.1044G>A (p.Ala348=) rs541549782 0.00002
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.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.1515C>T (p.Asp505=)
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
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.386+32944G>A
NM_004519.4(KCNQ3):c.60C>T (p.Gly20=)

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