| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42127619T>G | CA324665758 | CYP2D6 | c.799A>C (n.799A>C) c.1001A>C (p.Glu334Ala) c.848A>C (p.Glu283Ala) c.619A>C (n.619A>C) c.992A>C (p.Glu331Ala) n.1725A>C c.857A>C (p.Glu286Ala) c.859A>C (p.Arg287=) | dbSNP gnomAD v4 |
| 22 | g.42127619T= | CA2406578564 | CYP2D6 | c.799A= (n.799A=) c.1001A= (p.Glu334=) c.848A= (p.Glu283=) c.619A= (n.619A=) c.992A= (p.Glu331=) n.1725A= c.857A= (p.Glu286=) c.859A= (p.Arg287=) | dbSNP |