Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.12295960A>CCA362857212EDN1c.534-2A>C (n.534-2A>C)
c.531-2A>C (n.531-2A>C)
6g.12295960A>GCA362857210EDN1c.534-2A>G (n.534-2A>G)
c.531-2A>G (n.531-2A>G)
gnomAD v4 COSMIC
6g.12295960A>TCA362857211EDN1c.534-2A>T (n.534-2A>T)
c.531-2A>T (n.531-2A>T)
6g.12295961G>ACA362857213EDN1c.534-1G>A (n.534-1G>A)
c.531-1G>A (n.531-1G>A)
6g.12295961G>CCA362857214EDN1c.534-1G>C (n.534-1G>C)
c.531-1G>C (n.531-1G>C)
6g.12295961G>TCA362857215EDN1c.534-1G>T (n.534-1G>T)
c.531-1G>T (n.531-1G>T)
6g.12295962G>ACA448427932EDN1c.534G>A (p.Arg178=)
c.531G>A (p.Arg177=)
dbSNP gnomAD v2 gnomAD v4
6g.12295962G>CCA362857216EDN1c.534G>C (p.Arg178Ser)
c.531G>C (p.Arg177Ser)
6g.12295962G=CA1610830847EDN1c.534G= (p.Arg178=)
c.531G= (p.Arg177=)
6g.12295962G>TCA362857217EDN1c.534G>T (p.Arg178Ser)
c.531G>T (p.Arg177Ser)
ClinVar dbSNP
6g.12295963T>ACA362857218EDN1c.535T>A (p.Ser179Thr)
c.532T>A (p.Ser178Thr)
dbSNP gnomAD v2
6g.12295963T>CCA362857219EDN1c.535T>C (p.Ser179Pro)
c.532T>C (p.Ser178Pro)
6g.12295963T>GCA362857220EDN1c.535T>G (p.Ser179Ala)
c.532T>G (p.Ser178Ala)
6g.12295963T=CA1610830851EDN1c.535T= (p.Ser179=)
c.532T= (p.Ser178=)
6g.12295964C>ACA362857221EDN1c.536C>A (p.Ser179Ter)
c.533C>A (p.Ser178Ter)
dbSNP gnomAD v4
6g.12295964C=CA1610830853EDN1c.536C= (p.Ser179=)
c.533C= (p.Ser178=)
6g.12295964C>GCA362857222EDN1c.536C>G (p.Ser179Trp)
c.533C>G (p.Ser178Trp)
6g.12295964C>TCA3638759EDN1c.536C>T (p.Ser179Leu)
c.533C>T (p.Ser178Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.12295965G>ACA3638760EDN1c.537G>A (p.Ser179=)
c.534G>A (p.Ser178=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.12295965G>CCA448427933EDN1c.537G>C (p.Ser179=)
c.534G>C (p.Ser178=)
6g.12295965G=CA1610830857EDN1c.537G= (p.Ser179=)
c.534G= (p.Ser178=)
6g.12295965G>TCA448427934EDN1c.537G>T (p.Ser179=)
c.534G>T (p.Ser178=)
6g.12295966G>ACA362857225EDN1c.538G>A (p.Glu180Lys)
c.535G>A (p.Glu179Lys)
6g.12295966G>CCA362857224EDN1c.538G>C (p.Glu180Gln)
c.535G>C (p.Glu179Gln)
6g.12295966G>TCA362857223EDN1c.538G>T (p.Glu180Ter)
c.535G>T (p.Glu179Ter)
6g.12295967A>CCA362857227EDN1c.539A>C (p.Glu180Ala)
c.536A>C (p.Glu179Ala)
6g.12295967A>GCA362857226EDN1c.539A>G (p.Glu180Gly)
c.536A>G (p.Glu179Gly)
6g.12295967A>TCA362857228EDN1c.539A>T (p.Glu180Val)
c.536A>T (p.Glu179Val)
6g.12295968G>ACA448427935EDN1c.540G>A (p.Glu180=)
c.537G>A (p.Glu179=)
COSMIC
6g.12295968G>CCA362857229EDN1c.540G>C (p.Glu180Asp)
c.537G>C (p.Glu179Asp)
6g.12295968G=CA1610830863EDN1c.540G= (p.Glu180=)
c.537G= (p.Glu179=)
6g.12295968G>TCA362857230EDN1c.540G>T (p.Glu180Asp)
c.537G>T (p.Glu179Asp)
dbSNP gnomAD v2
6g.12295969A>CCA362857231EDN1c.541A>C (p.Thr181Pro)
c.538A>C (p.Thr180Pro)
6g.12295969A>GCA362857232EDN1c.541A>G (p.Thr181Ala)
c.538A>G (p.Thr180Ala)
6g.12295969A>TCA362857233EDN1c.541A>T (p.Thr181Ser)
c.538A>T (p.Thr180Ser)
6g.12295970C>ACA362857234EDN1c.542C>A (p.Thr181Asn)
c.539C>A (p.Thr180Asn)
dbSNP gnomAD v3 gnomAD v4
6g.12295970C=CA1610830865EDN1c.542C= (p.Thr181=)
c.539C= (p.Thr180=)
6g.12295970C>GCA362857235EDN1c.542C>G (p.Thr181Ser)
c.539C>G (p.Thr180Ser)
dbSNP
6g.12295970C>TCA362857236EDN1c.542C>T (p.Thr181Ile)
c.539C>T (p.Thr180Ile)
6g.12295971C>ACA3638761EDN1c.543C>A (p.Thr181=)
c.540C>A (p.Thr180=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.12295971C=CA1610830868EDN1c.543C= (p.Thr181=)
c.540C= (p.Thr180=)
6g.12295971C>GCA448427937EDN1c.543C>G (p.Thr181=)
c.540C>G (p.Thr180=)
6g.12295971C>TCA448427938EDN1c.543C>T (p.Thr181=)
c.540C>T (p.Thr180=)
dbSNP gnomAD v3 gnomAD v4
6g.12295972A=CA1610830870EDN1c.544A= (p.Met182=)
c.541A= (p.Met181=)
6g.12295972A>CCA3638762EDN1c.544A>C (p.Met182Leu)
c.541A>C (p.Met181Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.12295972A>GCA362857237EDN1c.544A>G (p.Met182Val)
c.541A>G (p.Met181Val)
6g.12295972A>TCA362857238EDN1c.544A>T (p.Met182Leu)
c.541A>T (p.Met181Leu)
6g.12295973T>ACA362857239EDN1c.545T>A (p.Met182Lys)
c.542T>A (p.Met181Lys)
6g.12295973T>CCA362857240EDN1c.545T>C (p.Met182Thr)
c.542T>C (p.Met181Thr)
gnomAD v4
6g.12295973T>GCA362857241EDN1c.545T>G (p.Met182Arg)
c.542T>G (p.Met181Arg)

Number of alleles fetched