Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.55279554G>ACA16620716TCF4c.652C>T (p.Gln218Ter)
c.172C>T (p.Gln58Ter)
n.332C>T
c.580C>T (p.Gln194Ter)
c.*360C>T (n.*360C>T)
c.262C>T (p.Gln88Ter)
c.*542C>T (n.*542C>T)
c.4C>T (p.Gln2Ter)
n.719C>T
n.346C>T
c.250C>T
c.682C>T (p.Gln228Ter)
c.*263C>T (n.*263C>T)
c.958C>T (p.Gln320Ter)
c.526C>T (p.Gln176Ter)
c.439C>T (p.Gln147Ter)
n.743C>T
n.507C>T
n.244C>T
c.670C>T (p.Gln224Ter)
c.400C>T (p.Gln134Ter)
n.401C>T
c.472C>T (p.Gln158Ter)
c.646C>T (p.Gln216Ter)
c.613C>T (p.Gln205Ter)
c.664C>T (p.Gln222Ter)
c.577C>T (p.Gln193Ter)
n.512C>T
n.524-18021C>T
c.421C>T (p.Gln141Ter)
c.442C>T (p.Gln148Ter)
n.451C>T
c.649C>T (p.Gln217Ter)
c.955C>T (p.Gln319Ter)
c.415C>T (p.Gln139Ter)
ClinVar dbSNP
18g.55279554G=CA2305026793TCF4c.652C= (p.Gln218=)
c.172C= (p.Gln58=)
n.332C=
c.580C= (p.Gln194=)
c.*360C= (n.*360C=)
c.262C= (p.Gln88=)
c.*542C= (n.*542C=)
c.4C= (p.Gln2=)
n.719C=
n.346C=
c.250C=
c.682C= (p.Gln228=)
c.*263C= (n.*263C=)
c.958C= (p.Gln320=)
c.526C= (p.Gln176=)
c.439C= (p.Gln147=)
n.743C=
n.507C=
n.244C=
c.670C= (p.Gln224=)
c.400C= (p.Gln134=)
n.401C=
c.472C= (p.Gln158=)
c.646C= (p.Gln216=)
c.613C= (p.Gln205=)
c.664C= (p.Gln222=)
c.577C= (p.Gln193=)
n.512C=
n.524-18021C=
c.421C= (p.Gln141=)
c.442C= (p.Gln148=)
n.451C=
c.649C= (p.Gln217=)
c.955C= (p.Gln319=)
c.415C= (p.Gln139=)
dbSNP

Number of alleles fetched