Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387423G>ACA473515653KCNJ11c.408C>T (p.Thr136=)
c.669C>T (p.Thr223=)
n.827C>T
dbSNP gnomAD v2
11g.17387423G>CCA5902264KCNJ11c.408C>G (p.Thr136=)
c.669C>G (p.Thr223=)
n.827C>G
dbSNP ExAC gnomAD v2 gnomAD v4
11g.17387423G=CA1955119256KCNJ11c.408C= (p.Thr136=)
c.669C= (p.Thr223=)
n.827C=
11g.17387423G>TCA473515654KCNJ11c.408C>A (p.Thr136=)
c.669C>A (p.Thr223=)
n.827C>A
11g.17387424G>ACA218399704KCNJ11c.407C>T (p.Thr136Ile)
c.668C>T (p.Thr223Ile)
n.826C>T
dbSNP gnomAD v3 gnomAD v4
11g.17387424G>CCA379771617KCNJ11c.407C>G (p.Thr136Ser)
c.668C>G (p.Thr223Ser)
n.826C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.17387424G=CA1955119257KCNJ11c.407C= (p.Thr136=)
c.668C= (p.Thr223=)
n.826C=
11g.17387424G>TCA379771613KCNJ11c.407C>A (p.Thr136Asn)
c.668C>A (p.Thr223Asn)
n.826C>A
gnomAD v4
11g.17387425T>ACA379771620KCNJ11c.406A>T (p.Thr136Ser)
c.667A>T (p.Thr223Ser)
n.825A>T
11g.17387425T>CCA379771623KCNJ11c.406A>G (p.Thr136Ala)
c.667A>G (p.Thr223Ala)
n.825A>G
11g.17387425T>GCA379771626KCNJ11c.406A>C (p.Thr136Pro)
c.667A>C (p.Thr223Pro)
n.825A>C
dbSNP
11g.17387425T=CA1955119258KCNJ11c.406A= (p.Thr136=)
c.667A= (p.Thr223=)
n.825A=
11g.17387426C>ACA379771631KCNJ11c.405G>T (p.Lys135Asn)
c.666G>T (p.Lys222Asn)
n.824G>T
11g.17387426C>GCA379771633KCNJ11c.405G>C (p.Lys135Asn)
c.666G>C (p.Lys222Asn)
n.824G>C
11g.17387426C>TCA473515655KCNJ11c.405G>A (p.Lys135=)
c.666G>A (p.Lys222=)
n.824G>A
11g.17387427T>ACA379771637KCNJ11c.404A>T (p.Lys135Met)
c.665A>T (p.Lys222Met)
n.823A>T
11g.17387427T>CCA379771640KCNJ11c.404A>G (p.Lys135Arg)
c.665A>G (p.Lys222Arg)
n.823A>G
11g.17387427T>GCA379771641KCNJ11c.404A>C (p.Lys135Thr)
c.665A>C (p.Lys222Thr)
n.823A>C
11g.17387428T>ACA379771644KCNJ11c.403A>T (p.Lys135Ter)
c.664A>T (p.Lys222Ter)
n.822A>T
11g.17387428T>CCA379771645KCNJ11c.403A>G (p.Lys135Glu)
c.664A>G (p.Lys222Glu)
n.822A>G
11g.17387428T>GCA5902265KCNJ11c.403A>C (p.Lys135Gln)
c.664A>C (p.Lys222Gln)
n.822A>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.17387428T=CA1955119259KCNJ11c.403A= (p.Lys135=)
c.664A= (p.Lys222=)
n.822A=
11g.17387429G>ACA473515658KCNJ11c.402C>T (p.Arg134=)
c.663C>T (p.Arg221=)
n.821C>T
11g.17387429G>CCA473515659KCNJ11c.402C>G (p.Arg134=)
c.663C>G (p.Arg221=)
n.821C>G
11g.17387429G>TCA473515660KCNJ11c.402C>A (p.Arg134=)
c.663C>A (p.Arg221=)
n.821C>A
ClinVar dbSNP
11g.17387430C>ACA218399706KCNJ11c.401G>T (p.Arg134Leu)
c.662G>T (p.Arg221Leu)
n.820G>T
dbSNP gnomAD v4 COSMIC
11g.17387430C=CA1955119260KCNJ11c.401G= (p.Arg134=)
c.662G= (p.Arg221=)
n.820G=
11g.17387430C>GCA379771653KCNJ11c.401G>C (p.Arg134Pro)
c.662G>C (p.Arg221Pro)
n.820G>C
ClinVar
11g.17387430C>TCA5902266KCNJ11c.401G>A (p.Arg134His)
c.662G>A (p.Arg221His)
n.820G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.17387431G>ACA5902267KCNJ11c.400C>T (p.Arg134Cys)
c.661C>T (p.Arg221Cys)
n.819C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.17387431G>CCA10605309KCNJ11c.400C>G (p.Arg134Gly)
c.661C>G (p.Arg221Gly)
n.819C>G
ClinVar dbSNP gnomAD v4
11g.17387431G=CA1955119261KCNJ11c.400C= (p.Arg134=)
c.661C= (p.Arg221=)
n.819C=
11g.17387431G>TCA5902268KCNJ11c.400C>A (p.Arg134Ser)
c.661C>A (p.Arg221Ser)
n.819C>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.17387432T>ACA473515662KCNJ11c.399A>T (p.Val133=)
c.660A>T (p.Val220=)
n.818A>T
11g.17387432T>CCA473515663KCNJ11c.399A>G (p.Val133=)
c.660A>G (p.Val220=)
n.818A>G
11g.17387432T>GCA473515664KCNJ11c.399A>C (p.Val133=)
c.660A>C (p.Val220=)
n.818A>C
11g.17387433A>CCA379771667KCNJ11c.398T>G (p.Val133Gly)
c.659T>G (p.Val220Gly)
n.817T>G
11g.17387433A>GCA379771677KCNJ11c.398T>C (p.Val133Ala)
c.659T>C (p.Val220Ala)
n.817T>C
11g.17387433A>TCA379771682KCNJ11c.398T>A (p.Val133Glu)
c.659T>A (p.Val220Glu)
n.817T>A
11g.17387434C>ACA379771683KCNJ11c.397G>T (p.Val133Leu)
c.658G>T (p.Val220Leu)
n.816G>T
11g.17387434C>GCA379771684KCNJ11c.397G>C (p.Val133Leu)
c.658G>C (p.Val220Leu)
n.816G>C
gnomAD v4
11g.17387434C>TCA379771686KCNJ11c.397G>A (p.Val133Ile)
c.658G>A (p.Val220Ile)
n.816G>A
gnomAD v4
11g.17387435C>ACA473515665KCNJ11c.396G>T (p.Val132=)
c.657G>T (p.Val219=)
n.815G>T
11g.17387435C>GCA473515666KCNJ11c.396G>C (p.Val132=)
c.657G>C (p.Val219=)
n.815G>C
11g.17387435C>TCA473515667KCNJ11c.396G>A (p.Val132=)
c.657G>A (p.Val219=)
n.815G>A
11g.17387436A>CCA379771692KCNJ11c.395T>G (p.Val132Gly)
c.656T>G (p.Val219Gly)
n.814T>G
11g.17387436A>GCA379771696KCNJ11c.395T>C (p.Val132Ala)
c.656T>C (p.Val219Ala)
n.814T>C
11g.17387436A>TCA379771700KCNJ11c.395T>A (p.Val132Glu)
c.656T>A (p.Val219Glu)
n.814T>A
11g.17387437C>ACA5902269KCNJ11c.394G>T (p.Val132Leu)
c.655G>T (p.Val219Leu)
n.813G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.17387437C=CA1955119262KCNJ11c.394G= (p.Val132=)
c.655G= (p.Val219=)
n.813G=

Number of alleles fetched