Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.12296048_12296053dupCA2578531343EDN1c.620_625dup (p.Asn208_Arg209insHisAsn)
c.617_622dup (p.Asn207_Arg208insHisAsn)
6g.12296046_12296056delinsCCACAACCGAGCA1610830999EDN1c.618_628delinsCCACAACCGAG (p.Thr206=)
c.615_625delinsCCACAACCGAG (p.Thr205=)
6g.12296051_12296060delCA3638777EDN1c.623_632del (p.Asn208IlefsTer10)
c.620_629del (p.Asn207IlefsTer10)
dbSNP ExAC gnomAD v2
6g.12296051A>CCA362857408EDN1c.623A>C (p.Asn208Thr)
c.620A>C (p.Asn207Thr)
6g.12296051A>GCA362857409EDN1c.623A>G (p.Asn208Ser)
c.620A>G (p.Asn207Ser)
6g.12296051A>TCA362857410EDN1c.623A>T (p.Asn208Ile)
c.620A>T (p.Asn207Ile)
6g.12296051_12296052delinsACCA1610831006EDN1c.623_624delinsAC (p.Asn208=)
c.620_621delinsAC (p.Asn207=)
6g.12296052C>ACA362857411EDN1c.624C>A (p.Asn208Lys)
c.621C>A (p.Asn207Lys)
gnomAD v4
6g.12296052C=CA1610831009EDN1c.624C= (p.Asn208=)
c.621C= (p.Asn207=)
6g.12296052C>GCA362857412EDN1c.624C>G (p.Asn208Lys)
c.621C>G (p.Asn207Lys)
6g.12296052C>TCA448427987EDN1c.624C>T (p.Asn208=)
c.621C>T (p.Asn207=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.12296053delCA1610831008EDN1c.625del (p.Arg209GlufsTer12)
c.622del (p.Arg208GlufsTer12)
dbSNP
6g.12296053C>ACA448427988EDN1c.625C>A (p.Arg209=)
c.622C>A (p.Arg208=)
6g.12296053C=CA1610831012EDN1c.625C= (p.Arg209=)
c.622C= (p.Arg208=)
6g.12296053C>GCA362857413EDN1c.625C>G (p.Arg209Gly)
c.622C>G (p.Arg208Gly)
gnomAD v4
6g.12296053C>TCA3638778EDN1c.625C>T (p.Arg209Ter)
c.622C>T (p.Arg208Ter)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.12296054G>ACA3638779EDN1c.626G>A (p.Arg209Gln)
c.623G>A (p.Arg208Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.12296054G>CCA362857415EDN1c.626G>C (p.Arg209Pro)
c.623G>C (p.Arg208Pro)
6g.12296054G=CA1610831013EDN1c.626G= (p.Arg209=)
c.623G= (p.Arg208=)
6g.12296054G>TCA362857414EDN1c.626G>T (p.Arg209Leu)
c.623G>T (p.Arg208Leu)
gnomAD v4
6g.12296055A>CCA448427991EDN1c.627A>C (p.Arg209=)
c.624A>C (p.Arg208=)
gnomAD v4
6g.12296055A>GCA448427990EDN1c.627A>G (p.Arg209=)
c.624A>G (p.Arg208=)
gnomAD v4
6g.12296055A>TCA448427989EDN1c.627A>T (p.Arg209=)
c.624A>T (p.Arg208=)
6g.12296056G>ACA362857416EDN1c.628G>A (p.Ala210Thr)
c.625G>A (p.Ala209Thr)
gnomAD v4
6g.12296056G>CCA362857417EDN1c.628G>C (p.Ala210Pro)
c.625G>C (p.Ala209Pro)
6g.12296056G>TCA362857418EDN1c.628G>T (p.Ala210Ser)
c.625G>T (p.Ala209Ser)
gnomAD v4
6g.12296057C>ACA362857419EDN1c.629C>A (p.Ala210Glu)
c.626C>A (p.Ala209Glu)
6g.12296057C=CA1610831016EDN1c.629C= (p.Ala210=)
c.626C= (p.Ala209=)
6g.12296057C>GCA362857420EDN1c.629C>G (p.Ala210Gly)
c.626C>G (p.Ala209Gly)
6g.12296057C>TCA362857421EDN1c.629C>T (p.Ala210Val)
c.626C>T (p.Ala209Val)
dbSNP gnomAD v3 gnomAD v4
6g.12296058A>CCA448427992EDN1c.630A>C (p.Ala210=)
c.627A>C (p.Ala209=)
6g.12296058A>GCA448427993EDN1c.630A>G (p.Ala210=)
c.627A>G (p.Ala209=)
6g.12296058A>TCA448427994EDN1c.630A>T (p.Ala210=)
c.627A>T (p.Ala209=)
6g.12296059C>ACA362857422EDN1c.631C>A (p.His211Asn)
c.628C>A (p.His210Asn)
6g.12296059C>GCA362857423EDN1c.631C>G (p.His211Asp)
c.628C>G (p.His210Asp)
6g.12296059C>TCA362857424EDN1c.631C>T (p.His211Tyr)
c.628C>T (p.His210Tyr)
6g.12296060A=CA1610831018EDN1c.632A= (p.His211=)
c.629A= (p.His210=)
6g.12296060A>CCA362857426EDN1c.632A>C (p.His211Pro)
c.629A>C (p.His210Pro)
6g.12296060A>GCA3638780EDN1c.632A>G (p.His211Arg)
c.629A>G (p.His210Arg)
dbSNP ExAC gnomAD v4
6g.12296060A>TCA362857425EDN1c.632A>T (p.His211Leu)
c.629A>T (p.His210Leu)
6g.12296061T>ACA362857427EDN1c.633T>A (p.His211Gln)
c.630T>A (p.His210Gln)
6g.12296061T>CCA3638781EDN1c.633T>C (p.His211=)
c.630T>C (p.His210=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.12296061T>GCA362857428EDN1c.633T>G (p.His211Gln)
c.630T>G (p.His210Gln)
dbSNP
6g.12296061T=CA1610831021EDN1c.633T= (p.His211=)
c.630T= (p.His210=)
6g.12296062T>ACA362857429EDN1c.634T>A (p.Trp212Arg)
c.631T>A (p.Trp211Arg)
6g.12296062T>CCA3638782EDN1c.634T>C (p.Trp212Arg)
c.631T>C (p.Trp211Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.12296062T>GCA362857430EDN1c.634T>G (p.Trp212Gly)
c.631T>G (p.Trp211Gly)
6g.12296062T=CA1610831026EDN1c.634T= (p.Trp212=)
c.631T= (p.Trp211=)
6g.12296063G>ACA362857431EDN1c.635G>A (p.Trp212Ter)
c.632G>A (p.Trp211Ter)
6g.12296063G>CCA362857432EDN1c.635G>C (p.Trp212Ser)
c.632G>C (p.Trp211Ser)

Number of alleles fetched