Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387583T>ACA379773151KCNJ11c.248A>T (p.Lys83Met)
c.509A>T (p.Lys170Met)
n.667A>T
11g.17387583T>CCA340805KCNJ11c.248A>G (p.Lys83Arg)
c.509A>G (p.Lys170Arg)
n.667A>G
ClinVar dbSNP
11g.17387583T>GCA379773156KCNJ11c.248A>C (p.Lys83Thr)
c.509A>C (p.Lys170Thr)
n.667A>C
11g.17387583T=CA1955119320KCNJ11c.248A= (p.Lys83=)
c.509A= (p.Lys170=)
n.667A=
11g.17387584T>ACA379773160KCNJ11c.247A>T (p.Lys83Ter)
c.508A>T (p.Lys170Ter)
n.666A>T
11g.17387584T>CCA379773161KCNJ11c.247A>G (p.Lys83Glu)
c.508A>G (p.Lys170Glu)
n.666A>G
dbSNP gnomAD v2 gnomAD v4
11g.17387584T>GCA379773162KCNJ11c.247A>C (p.Lys83Gln)
c.508A>C (p.Lys170Gln)
n.666A>C
11g.17387584T=CA1955119321KCNJ11c.247A= (p.Lys83=)
c.508A= (p.Lys170=)
n.666A=
11g.17387585C>ACA379773163KCNJ11c.246G>T (p.Met82Ile)
c.507G>T (p.Met169Ile)
n.665G>T
11g.17387585C>GCA379773164KCNJ11c.246G>C (p.Met82Ile)
c.507G>C (p.Met169Ile)
n.665G>C
11g.17387585C>TCA379773165KCNJ11c.246G>A (p.Met82Ile)
c.507G>A (p.Met169Ile)
n.665G>A
11g.17387586A>CCA379773171KCNJ11c.245T>G (p.Met82Arg)
c.506T>G (p.Met169Arg)
n.664T>G
11g.17387586A>GCA379773168KCNJ11c.245T>C (p.Met82Thr)
c.506T>C (p.Met169Thr)
n.664T>C
11g.17387586A>TCA379773167KCNJ11c.245T>A (p.Met82Lys)
c.506T>A (p.Met169Lys)
n.664T>A
11g.17387587T>ACA379773174KCNJ11c.244A>T (p.Met82Leu)
c.505A>T (p.Met169Leu)
n.663A>T
11g.17387587T>CCA379773182KCNJ11c.244A>G (p.Met82Val)
c.505A>G (p.Met169Val)
n.663A>G
gnomAD v4
11g.17387587T>GCA379773183KCNJ11c.244A>C (p.Met82Leu)
c.505A>C (p.Met169Leu)
n.663A>C
11g.17387588G>ACA473515514KCNJ11c.243C>T (p.Phe81=)
c.504C>T (p.Phe168=)
n.662C>T
11g.17387588G>CCA379773184KCNJ11c.243C>G (p.Phe81Leu)
c.504C>G (p.Phe168Leu)
n.662C>G
11g.17387588G>TCA379773185KCNJ11c.243C>A (p.Phe81Leu)
c.504C>A (p.Phe168Leu)
n.662C>A
11g.17387589A>CCA379773190KCNJ11c.242T>G (p.Phe81Cys)
c.503T>G (p.Phe168Cys)
n.661T>G
11g.17387589A>GCA379773192KCNJ11c.242T>C (p.Phe81Ser)
c.503T>C (p.Phe168Ser)
n.661T>C
11g.17387589A>TCA379773194KCNJ11c.242T>A (p.Phe81Tyr)
c.503T>A (p.Phe168Tyr)
n.661T>A
11g.17387590A>CCA379773198KCNJ11c.241T>G (p.Phe81Val)
c.502T>G (p.Phe168Val)
n.660T>G
11g.17387590A>GCA379773200KCNJ11c.241T>C (p.Phe81Leu)
c.502T>C (p.Phe168Leu)
n.660T>C
11g.17387590A>TCA379773202KCNJ11c.241T>A (p.Phe81Ile)
c.502T>A (p.Phe168Ile)
n.660T>A
11g.17387591G>ACA473515515KCNJ11c.240C>T (p.Ile80=)
c.501C>T (p.Ile167=)
n.659C>T
11g.17387591G>CCA379773205KCNJ11c.240C>G (p.Ile80Met)
c.501C>G (p.Ile167Met)
n.659C>G
COSMIC
11g.17387591G>TCA473515516KCNJ11c.240C>A (p.Ile80=)
c.501C>A (p.Ile167=)
n.659C>A
11g.17387592A>CCA379773213KCNJ11c.239T>G (p.Ile80Ser)
c.500T>G (p.Ile167Ser)
n.658T>G
11g.17387592A>GCA379773211KCNJ11c.239T>C (p.Ile80Thr)
c.500T>C (p.Ile167Thr)
n.658T>C
11g.17387592A>TCA379773210KCNJ11c.239T>A (p.Ile80Asn)
c.500T>A (p.Ile167Asn)
n.658T>A
gnomAD v4
11g.17387593T>ACA379773218KCNJ11c.238A>T (p.Ile80Phe)
c.499A>T (p.Ile167Phe)
n.657A>T
11g.17387593T>CCA379773217KCNJ11c.238A>G (p.Ile80Val)
c.499A>G (p.Ile167Val)
n.657A>G
11g.17387593T>GCA119835KCNJ11c.238A>C (p.Ile80Leu)
c.499A>C (p.Ile167Leu)
n.657A>C
ClinVar dbSNP
11g.17387593T=CA1955119322KCNJ11c.238A= (p.Ile80=)
c.499A= (p.Ile167=)
n.657A=
11g.17387594G>ACA473515517KCNJ11c.237C>T (p.Cys79=)
c.498C>T (p.Cys166=)
n.656C>T
11g.17387594G>CCA172328KCNJ11c.237C>G (p.Cys79Trp)
c.498C>G (p.Cys166Trp)
n.656C>G
ClinVar dbSNP
11g.17387594G=CA1955119323KCNJ11c.237C= (p.Cys79=)
c.498C= (p.Cys166=)
n.656C=
11g.17387594G>TCA379773220KCNJ11c.237C>A (p.Cys79Ter)
c.498C>A (p.Cys166Ter)
n.656C>A
ClinVar dbSNP
11g.17387595C>ACA119833KCNJ11c.236G>T (p.Cys79Phe)
c.497G>T (p.Cys166Phe)
n.655G>T
ClinVar dbSNP
11g.17387595C=CA1955119324KCNJ11c.236G= (p.Cys79=)
c.497G= (p.Cys166=)
n.655G=
11g.17387595C>GCA379773227KCNJ11c.236G>C (p.Cys79Ser)
c.497G>C (p.Cys166Ser)
n.655G>C
11g.17387595C>TCA341720KCNJ11c.236G>A (p.Cys79Tyr)
c.497G>A (p.Cys166Tyr)
n.655G>A
ClinVar dbSNP
11g.17387596A>CCA379773233KCNJ11c.235T>G (p.Cys79Gly)
c.496T>G (p.Cys166Gly)
n.654T>G
11g.17387596A>GCA379773235KCNJ11c.235T>C (p.Cys79Arg)
c.496T>C (p.Cys166Arg)
n.654T>C
11g.17387596A>TCA379773238KCNJ11c.235T>A (p.Cys79Ser)
c.496T>A (p.Cys166Ser)
n.654T>A
11g.17387597G>ACA473515518KCNJ11c.234C>T (p.Gly78=)
c.495C>T (p.Gly165=)
n.653C>T
ClinVar dbSNP gnomAD v4
11g.17387597G>CCA473515519KCNJ11c.234C>G (p.Gly78=)
c.495C>G (p.Gly165=)
n.653C>G
11g.17387597G>TCA473515520KCNJ11c.234C>A (p.Gly78=)
c.495C>A (p.Gly165=)
n.653C>A

Number of alleles fetched