Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128185C>T | CA10264854 | CYP2D6 | c.679G>A (p.Glu227Lys) c.832G>A (p.Glu278Lys) c.499G>A (p.Glu167Lys) c.766G>A (p.Glu256Lys) n.1556G>A c.688G>A (p.Glu230Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128185C= | CA2406578985 | CYP2D6 | c.679G= (p.Glu227=) c.832G= (p.Glu278=) c.499G= (p.Glu167=) c.766G= (p.Glu256=) n.1556G= c.688G= (p.Glu230=) | dbSNP |