ClinVar Miner

List of variants in gene KCNJ10 reported as likely benign for not specified

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_002241.5(KCNJ10):c.811C>T (p.Arg271Cys) rs1130183 0.04770
NM_002241.5(KCNJ10):c.53G>A (p.Arg18Gln) rs115466046 0.01096
NM_002241.5(KCNJ10):c.812G>A (p.Arg271His) rs3795339 0.00113
NM_002241.5(KCNJ10):c.615A>G (p.Lys205=) rs142228240 0.00066
NM_002241.5(KCNJ10):c.219G>A (p.Ala73=) rs144495959 0.00016
NM_002241.5(KCNJ10):c.114C>T (p.Asn38=) rs151068619 0.00008
NM_002241.5(KCNJ10):c.225T>C (p.Phe75=) rs757159382 0.00006
NM_002241.5(KCNJ10):c.528T>C (p.Ala176=) rs1057520295 0.00002
NM_002241.5(KCNJ10):c.-1+11G>A rs765287915 0.00001
NM_002241.5(KCNJ10):c.1-20T>G rs752563712 0.00001
NM_002241.5(KCNJ10):c.117G>T (p.Val39=) rs898999212 0.00001
NM_002241.5(KCNJ10):c.501G>A (p.Ala167=) rs200522826 0.00001
NM_002241.5(KCNJ10):c.762C>A (p.Thr254=) rs569080326 0.00001
NM_002241.5(KCNJ10):c.-36G>T rs1194219402
NM_002241.5(KCNJ10):c.117G>C (p.Val39=) rs898999212
NM_002241.5(KCNJ10):c.147C>T (p.Phe49=) rs1057523361
NM_002241.5(KCNJ10):c.300C>T (p.Asp100=) rs139069413
NM_002241.5(KCNJ10):c.39T>C (p.Thr13=) rs776805483
NM_002241.5(KCNJ10):c.465C>T (p.Thr155=) rs1553235032

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