Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.155659923C>GCA342764186YY1AP1c.1987G>C (p.Glu663Gln)
c.2125G>C (p.Glu709Gln)
c.1894G>C (p.Glu632Gln)
c.*1251G>C (n.*1251G>C)
c.1954G>C (p.Glu652Gln)
c.*1485G>C (n.*1485G>C)
c.2401G>C (p.Glu801Gln)
c.2341G>C (p.Glu781Gln)
c.1927G>C (p.Glu643Gln)
c.*1996G>C (n.*1996G>C)
n.2031G>C
n.323G>C
c.*930G>C (n.*930G>C)
c.1789G>C (p.Glu597Gln)
c.2185G>C (p.Glu729Gln)
dbSNP
1g.155659923C>ACA16044406YY1AP1c.1987G>T (p.Glu663Ter)
c.2125G>T (p.Glu709Ter)
c.1894G>T (p.Glu632Ter)
c.*1251G>T (n.*1251G>T)
c.1954G>T (p.Glu652Ter)
c.*1485G>T (n.*1485G>T)
c.2401G>T (p.Glu801Ter)
c.2341G>T (p.Glu781Ter)
c.1927G>T (p.Glu643Ter)
c.*1996G>T (n.*1996G>T)
n.2031G>T
n.323G>T
c.*930G>T (n.*930G>T)
c.1789G>T (p.Glu597Ter)
c.2185G>T (p.Glu729Ter)
ClinVar dbSNP

Number of alleles fetched