Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.73418269del | CA170815 | ALB | c.1610del (p.Ile537AsnfsTer21) c.1265del (p.Ile422AsnfsTer21) c.1034del (p.Ile345AsnfsTer21) c.*889del (n.*889del) n.264del c.1160del (p.Ile387AsnfsTer21) n.1157del c.1143del c.971del (p.Ile324AsnfsTer21) | ClinVar dbSNP |
4 | g.73418269T= | CA1468146972 | ALB | c.1610T= (p.Ile537=) c.1265T= (p.Ile422=) c.1034T= (p.Ile345=) c.*889T= (n.*889T=) n.264T= c.1160T= (p.Ile387=) n.1157T= c.1143T= c.971T= (p.Ile324=) | dbSNP dbSNP |