ClinVar Miner

List of variants in gene KCNQ3 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.1994C>T (p.Ser665Leu) rs147173555 0.00165
NM_004519.4(KCNQ3):c.1917C>T (p.Leu639=) rs78731303 0.00131
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831 0.00043
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910 0.00034
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246 0.00031
NM_004519.4(KCNQ3):c.225C>G (p.Asp75Glu) rs138254004 0.00029
NM_004519.4(KCNQ3):c.834T>C (p.Leu278=) rs769657433 0.00020
NM_004519.4(KCNQ3):c.1964C>T (p.Thr655Met) rs199942237 0.00019
NM_004519.4(KCNQ3):c.2499C>T (p.Leu833=) rs773301064 0.00011
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.1656C>T (p.Ala552=) rs199722269 0.00006
NM_004519.4(KCNQ3):c.2614A>G (p.Ile872Val) rs199682667 0.00006
NM_004519.4(KCNQ3):c.1590T>C (p.Tyr530=) rs757378151 0.00005
NM_004519.4(KCNQ3):c.1216G>A (p.Val406Ile) rs144474368 0.00004
NM_004519.4(KCNQ3):c.1665C>T (p.Leu555=) rs143511163 0.00004
NM_004519.4(KCNQ3):c.1677C>A (p.Ser559=) rs377613824 0.00004
NM_004519.4(KCNQ3):c.2505G>C (p.Glu835Asp) rs748320350 0.00004
NM_004519.4(KCNQ3):c.616C>T (p.Leu206=) rs770952684 0.00004
NM_004519.4(KCNQ3):c.1617G>A (p.Arg539=) rs140607300 0.00003
NM_004519.4(KCNQ3):c.1403A>G (p.Asn468Ser) rs118192252 0.00002
NM_004519.4(KCNQ3):c.1443C>T (p.Tyr481=) rs200812594 0.00002
NM_004519.4(KCNQ3):c.1471G>A (p.Gly491Arg) rs201552546 0.00002
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988 0.00002
NM_004519.4(KCNQ3):c.1020C>T (p.Gly340=) rs1490473853 0.00001
NM_004519.4(KCNQ3):c.1775C>G (p.Thr592Ser) rs556421495 0.00001
NM_004519.4(KCNQ3):c.1938C>T (p.His646=) rs759859458 0.00001
NM_004519.4(KCNQ3):c.2562G>A (p.Ser854=) rs201736771 0.00001
NM_004519.4(KCNQ3):c.42C>T (p.Gly14=) rs1395792790 0.00001
NM_004519.4(KCNQ3):c.789G>A (p.Thr263=) rs762086066 0.00001
NM_004519.4(KCNQ3):c.978G>A (p.Thr326=) rs751628183 0.00001
NM_004519.4(KCNQ3):c.98C>T (p.Ala33Val) rs761196042 0.00001
NM_004519.4(KCNQ3):c.1158T>C (p.Tyr386=)
NM_004519.4(KCNQ3):c.1822C>G (p.Pro608Ala)
NM_004519.4(KCNQ3):c.1885G>A (p.Val629Ile) rs185511111
NM_004519.4(KCNQ3):c.1958A>G (p.Gln653Arg) rs554833870
NM_004519.4(KCNQ3):c.233A>T (p.Gln78Leu)
NM_004519.4(KCNQ3):c.2463T>C (p.Asn821=)
NM_004519.4(KCNQ3):c.2514G>C (p.Thr838=) rs568466967
NM_004519.4(KCNQ3):c.483A>T (p.Thr161=)
NM_004519.4(KCNQ3):c.56_73del (p.Gly19_Gly24del) rs774616642
NM_004519.4(KCNQ3):c.609C>T (p.Ile203=) rs574174380
NM_004519.4(KCNQ3):c.77C>T (p.Ala26Val)

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