ClinVar Miner

List of variants in gene KCNJ5 reported as likely benign for Cardiovascular phenotype

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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_000890.5(KCNJ5):c.192C>T (p.His64=) rs140848236 0.00182
NM_000890.5(KCNJ5):c.837G>A (p.Glu279=) rs149861510 0.00087
NM_000890.5(KCNJ5):c.1149C>T (p.Pro383=) rs143219149 0.00078
NM_000890.5(KCNJ5):c.957G>A (p.Arg319=) rs192889782 0.00051
NM_000890.5(KCNJ5):c.273C>T (p.Leu91=) rs146853795 0.00037
NM_000890.5(KCNJ5):c.744G>A (p.Glu248=) rs144040058 0.00037
NM_000890.5(KCNJ5):c.825C>A (p.Ile275=) rs113012271 0.00034
NM_000890.5(KCNJ5):c.1158G>C (p.Leu386=) rs141325005 0.00026
NM_000890.5(KCNJ5):c.645G>A (p.Leu215=) rs147245544 0.00021
NM_000890.5(KCNJ5):c.1123C>T (p.Arg375Trp) rs142454198 0.00017
NM_000890.5(KCNJ5):c.630G>A (p.Met210Ile) rs138295501 0.00016
NM_000890.5(KCNJ5):c.133G>A (p.Glu45Lys) rs372447456 0.00011
NM_000890.5(KCNJ5):c.1152A>G (p.Pro384=) rs987098040 0.00010
NM_000890.5(KCNJ5):c.312C>T (p.Phe104=) rs201217363 0.00009
NM_000890.5(KCNJ5):c.792C>T (p.Gly264=) rs750600982 0.00009
NM_000890.5(KCNJ5):c.738G>A (p.Glu246=) rs372736753 0.00008
NM_000890.5(KCNJ5):c.53C>T (p.Thr18Ile) rs375669366 0.00006
NM_000890.5(KCNJ5):c.1124G>A (p.Arg375Gln) rs530587789 0.00005
NM_000890.5(KCNJ5):c.1254G>A (p.Ser418=) rs528463709 0.00005
NM_000890.5(KCNJ5):c.739G>A (p.Gly247Arg) rs200170681 0.00005
NM_000890.5(KCNJ5):c.843C>T (p.Asn281=) rs370673577 0.00005
NM_000890.5(KCNJ5):c.1230T>G (p.Gly410=) rs772009654 0.00003
NM_000890.5(KCNJ5):c.351C>T (p.Asp117=) rs765873474 0.00003
NM_000890.5(KCNJ5):c.438C>T (p.Thr146=) rs140697732 0.00003
NM_000890.5(KCNJ5):c.591G>A (p.Ala197=) rs750048771 0.00003
NM_000890.5(KCNJ5):c.615C>T (p.Asn205=) rs370546974 0.00003
NM_000890.5(KCNJ5):c.430A>G (p.Ile144Val) rs369703183 0.00002
NM_000890.5(KCNJ5):c.1137C>T (p.Tyr379=) rs781130958 0.00001
NM_000890.5(KCNJ5):c.1155G>T (p.Leu385=) rs1202155314 0.00001
NM_000890.5(KCNJ5):c.183C>T (p.Asn61=) rs760931417 0.00001
NM_000890.5(KCNJ5):c.198C>T (p.Asn66=) rs371347693 0.00001
NM_000890.5(KCNJ5):c.214C>T (p.Arg72Trp) rs757877367 0.00001
NM_000890.5(KCNJ5):c.408C>T (p.Phe136=) rs780052854 0.00001
NM_000890.5(KCNJ5):c.414C>T (p.Ser138=) rs149219318 0.00001
NM_000890.5(KCNJ5):c.618A>G (p.Ala206=) rs758377412 0.00001
NM_000890.5(KCNJ5):c.724C>T (p.Arg242Trp) rs576156828 0.00001
NM_000890.5(KCNJ5):c.732C>T (p.Thr244=) rs545729688 0.00001
NM_000890.5(KCNJ5):c.906G>T (p.Val302=) rs533482437 0.00001
NM_000890.5(KCNJ5):c.90C>T (p.Arg30=) rs201886526 0.00001
NM_000890.5(KCNJ5):c.1098G>A (p.Glu366=)
NM_000890.5(KCNJ5):c.1140C>T (p.Leu380=)
NM_000890.5(KCNJ5):c.1152A>C (p.Pro384=)
NM_000890.5(KCNJ5):c.115C>T (p.Arg39Cys)
NM_000890.5(KCNJ5):c.1218C>T (p.Pro406=)
NM_000890.5(KCNJ5):c.1237A>C (p.Arg413=)
NM_000890.5(KCNJ5):c.132C>T (p.Ala44=) rs757867512
NM_000890.5(KCNJ5):c.240C>G (p.Thr80=)
NM_000890.5(KCNJ5):c.297C>T (p.Val99=)
NM_000890.5(KCNJ5):c.336T>C (p.Ala112=)
NM_000890.5(KCNJ5):c.456T>C (p.Tyr152=)
NM_000890.5(KCNJ5):c.459C>T (p.Gly153=)
NM_000890.5(KCNJ5):c.501C>G (p.Leu167=)
NM_000890.5(KCNJ5):c.621C>T (p.Val207=)
NM_000890.5(KCNJ5):c.631C>A (p.Arg211=)
NM_000890.5(KCNJ5):c.681C>T (p.Ser227=)
NM_000890.5(KCNJ5):c.741G>A (p.Gly247=)
NM_000890.5(KCNJ5):c.741G>C (p.Gly247=)
NM_000890.5(KCNJ5):c.768C>T (p.Asp256=)
NM_000890.5(KCNJ5):c.771C>T (p.Ile257=)
NM_000890.5(KCNJ5):c.774C>T (p.Asn258=)
NM_000890.5(KCNJ5):c.789G>A (p.Thr263=)
NM_000890.5(KCNJ5):c.840C>T (p.Ile280=)
NM_000890.5(KCNJ5):c.87C>T (p.Ala29=)
NM_000890.5(KCNJ5):c.900A>G (p.Glu300=)
NM_000890.5(KCNJ5):c.96T>C (p.Tyr32=) rs767651199

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