Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387321_17387327dupCA658822453KCNJ11c.504_510dup (p.Tyr171AspfsTer7)
c.765_771dup (p.Tyr258AspfsTer7)
n.923_929dup
ClinVar dbSNP
11g.17387325A>CCA379770900KCNJ11c.506T>G (p.Ile169Ser)
c.767T>G (p.Ile256Ser)
n.925T>G
11g.17387325A>GCA379770902KCNJ11c.506T>C (p.Ile169Thr)
c.767T>C (p.Ile256Thr)
n.925T>C
11g.17387325A>TCA379770904KCNJ11c.506T>A (p.Ile169Asn)
c.767T>A (p.Ile256Asn)
n.925T>A
11g.17387326T>ACA379770909KCNJ11c.505A>T (p.Ile169Phe)
c.766A>T (p.Ile256Phe)
n.924A>T
11g.17387326T>CCA379770911KCNJ11c.505A>G (p.Ile169Val)
c.766A>G (p.Ile256Val)
n.924A>G
11g.17387326T>GCA379770914KCNJ11c.505A>C (p.Ile169Leu)
c.766A>C (p.Ile256Leu)
n.924A>C
11g.17387327C>ACA473515440KCNJ11c.504G>T (p.Leu168=)
c.765G>T (p.Leu255=)
n.923G>T
dbSNP
11g.17387327C=CA1955119214KCNJ11c.504G= (p.Leu168=)
c.765G= (p.Leu255=)
n.923G=
11g.17387327C>GCA473515441KCNJ11c.504G>C (p.Leu168=)
c.765G>C (p.Leu255=)
n.923G>C
11g.17387327C>TCA473515442KCNJ11c.504G>A (p.Leu168=)
c.765G>A (p.Leu255=)
n.923G>A
dbSNP gnomAD v2
11g.17387328A>CCA379770917KCNJ11c.503T>G (p.Leu168Arg)
c.764T>G (p.Leu255Arg)
n.922T>G
11g.17387328A>GCA379770920KCNJ11c.503T>C (p.Leu168Pro)
c.764T>C (p.Leu255Pro)
n.922T>C
11g.17387328A>TCA379770923KCNJ11c.503T>A (p.Leu168Gln)
c.764T>A (p.Leu255Gln)
n.922T>A
11g.17387329G>ACA473515443KCNJ11c.502C>T (p.Leu168=)
c.763C>T (p.Leu255=)
n.921C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.17387329G>CCA379770924KCNJ11c.502C>G (p.Leu168Val)
c.763C>G (p.Leu255Val)
n.921C>G
11g.17387329G=CA1955119215KCNJ11c.502C= (p.Leu168=)
c.763C= (p.Leu255=)
n.921C=
11g.17387329G>TCA379770927KCNJ11c.502C>A (p.Leu168Met)
c.763C>A (p.Leu255Met)
n.921C>A
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.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.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

Number of alleles fetched