Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387330delCA3003288822KCNJ11c.501del (p.Leu168Ter)
c.762del (p.Leu255Ter)
n.920del
11g.17387330C>ACA473515444KCNJ11c.501G>T (p.Pro167=)
c.762G>T (p.Pro254=)
n.920G>T
11g.17387330C=CA1955119216KCNJ11c.501G= (p.Pro167=)
c.762G= (p.Pro254=)
n.920G=
11g.17387330C>GCA473515445KCNJ11c.501G>C (p.Pro167=)
c.762G>C (p.Pro254=)
n.920G>C
11g.17387330C>TCA5902251KCNJ11c.501G>A (p.Pro167=)
c.762G>A (p.Pro254=)
n.920G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.17387331G>ACA254520KCNJ11c.500C>T (p.Pro167Leu)
c.761C>T (p.Pro254Leu)
n.919C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.17387331G>CCA379770937KCNJ11c.500C>G (p.Pro167Arg)
c.761C>G (p.Pro254Arg)
n.919C>G
11g.17387331G=CA1955119217KCNJ11c.500C= (p.Pro167=)
c.761C= (p.Pro254=)
n.919C=
11g.17387331G>TCA379770938KCNJ11c.500C>A (p.Pro167Gln)
c.761C>A (p.Pro254Gln)
n.919C>A
11g.17387334dupCA3003288829KCNJ11c.500dup (p.Leu168AlafsTer8)
c.761dup (p.Leu255AlafsTer8)
n.919dup
11g.17387334delCA3003288827KCNJ11c.500del (p.Pro167ArgfsTer2)
c.761del (p.Pro254ArgfsTer2)
n.919del
11g.17387332G>ACA379770942KCNJ11c.499C>T (p.Pro167Ser)
c.760C>T (p.Pro254Ser)
n.918C>T
gnomAD v4
11g.17387332G>CCA379770944KCNJ11c.499C>G (p.Pro167Ala)
c.760C>G (p.Pro254Ala)
n.918C>G
11g.17387332G>TCA379770946KCNJ11c.499C>A (p.Pro167Thr)
c.760C>A (p.Pro254Thr)
n.918C>A
11g.17387333G>ACA5902252KCNJ11c.498C>T (p.Ala166=)
c.759C>T (p.Ala253=)
n.917C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.17387333G>CCA5902253KCNJ11c.498C>G (p.Ala166=)
c.759C>G (p.Ala253=)
n.917C>G
dbSNP ExAC gnomAD v2
11g.17387333G=CA1955119218KCNJ11c.498C= (p.Ala166=)
c.759C= (p.Ala253=)
n.917C=
11g.17387333G>TCA473515449KCNJ11c.498C>A (p.Ala166=)
c.759C>A (p.Ala253=)
n.917C>A
11g.17387334G>ACA379770953KCNJ11c.497C>T (p.Ala166Val)
c.758C>T (p.Ala253Val)
n.916C>T
dbSNP gnomAD v4
11g.17387334G>CCA379770955KCNJ11c.497C>G (p.Ala166Gly)
c.758C>G (p.Ala253Gly)
n.916C>G
11g.17387334G=CA1955119219KCNJ11c.497C= (p.Ala166=)
c.758C= (p.Ala253=)
n.916C=
11g.17387334G>TCA379770969KCNJ11c.497C>A (p.Ala166Asp)
c.758C>A (p.Ala253Asp)
n.916C>A
gnomAD v4
11g.17387335C>ACA379770976KCNJ11c.496G>T (p.Ala166Ser)
c.757G>T (p.Ala253Ser)
n.915G>T
gnomAD v4
11g.17387335C>GCA379770979KCNJ11c.496G>C (p.Ala166Pro)
c.757G>C (p.Ala253Pro)
n.915G>C
11g.17387335C>TCA379770974KCNJ11c.496G>A (p.Ala166Thr)
c.757G>A (p.Ala253Thr)
n.915G>A
gnomAD v4
11g.17387336delCA3003288852KCNJ11c.496del (p.Ala166ProfsTer3)
c.757del (p.Ala253ProfsTer3)
n.915del
11g.17387336C>ACA473515454KCNJ11c.495G>T (p.Val165=)
c.756G>T (p.Val252=)
n.914G>T
11g.17387336C>GCA473515455KCNJ11c.495G>C (p.Val165=)
c.756G>C (p.Val252=)
n.914G>C
11g.17387336C>TCA473515456KCNJ11c.495G>A (p.Val165=)
c.756G>A (p.Val252=)
n.914G>A
11g.17387337delCA2612638705KCNJ11c.494del (p.Val165GlyfsTer4)
c.755del (p.Val252GlyfsTer4)
n.913del
gnomAD v4
11g.17387337A=CA1955119220KCNJ11c.494T= (p.Val165=)
c.755T= (p.Val252=)
n.913T=
11g.17387337A>CCA379770983KCNJ11c.494T>G (p.Val165Gly)
c.755T>G (p.Val252Gly)
n.913T>G
11g.17387337A>GCA341726KCNJ11c.494T>C (p.Val165Ala)
c.755T>C (p.Val252Ala)
n.913T>C
ClinVar dbSNP
11g.17387337A>TCA379770987KCNJ11c.494T>A (p.Val165Glu)
c.755T>A (p.Val252Glu)
n.913T>A
11g.17387338C>ACA379770990KCNJ11c.493G>T (p.Val165Leu)
c.754G>T (p.Val252Leu)
n.912G>T
ClinVar dbSNP
11g.17387338C>GCA379770993KCNJ11c.493G>C (p.Val165Leu)
c.754G>C (p.Val252Leu)
n.912G>C
11g.17387338C>TCA379770996KCNJ11c.493G>A (p.Val165Met)
c.754G>A (p.Val252Met)
n.912G>A
11g.17387339delCA3003288854KCNJ11c.493del (p.Val165TrpfsTer4)
c.754del (p.Val252TrpfsTer4)
n.912del
11g.17387339C>ACA473515458KCNJ11c.492G>T (p.Leu164=)
c.753G>T (p.Leu251=)
n.911G>T
11g.17387339C=CA1955119221KCNJ11c.492G= (p.Leu164=)
c.753G= (p.Leu251=)
n.911G=
11g.17387339C>GCA5902254KCNJ11c.492G>C (p.Leu164=)
c.753G>C (p.Leu251=)
n.911G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.17387339C>TCA473515459KCNJ11c.492G>A (p.Leu164=)
c.753G>A (p.Leu251=)
n.911G>A
11g.17387340delCA3003288855KCNJ11c.491del (p.Leu164ArgfsTer5)
c.752del (p.Leu251ArgfsTer5)
n.910del
11g.17387340A>CCA379771004KCNJ11c.491T>G (p.Leu164Arg)
c.752T>G (p.Leu251Arg)
n.910T>G
11g.17387340A>GCA379771008KCNJ11c.491T>C (p.Leu164Pro)
c.752T>C (p.Leu251Pro)
n.910T>C
11g.17387340A>TCA379771005KCNJ11c.491T>A (p.Leu164Gln)
c.752T>A (p.Leu251Gln)
n.910T>A
11g.17387341G>ACA473515460KCNJ11c.490C>T (p.Leu164=)
c.751C>T (p.Leu251=)
n.909C>T
11g.17387341G>CCA379771010KCNJ11c.490C>G (p.Leu164Val)
c.751C>G (p.Leu251Val)
n.909C>G
11g.17387341G>TCA379771011KCNJ11c.490C>A (p.Leu164Met)
c.751C>A (p.Leu251Met)
n.909C>A
11g.17387342G>ACA473515461KCNJ11c.489C>T (p.Phe163=)
c.750C>T (p.Phe250=)
n.908C>T
dbSNP

Number of alleles fetched