| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42126627A>G | CA411769847 | CYP2D6 | c.1239T>C (n.1239T>C) c.1441T>C (p.Phe481Leu) c.1288T>C (p.Phe430Leu) c.1059T>C (n.1059T>C) c.1432T>C (p.Phe478Leu) n.2165T>C c.1297T>C (p.Phe433Leu) | ClinVar dbSNP |
| 22 | g.42126627A= | CA2406577822 | CYP2D6 | c.1239T= (n.1239T=) c.1441T= (p.Phe481=) c.1288T= (p.Phe430=) c.1059T= (n.1059T=) c.1432T= (p.Phe478=) n.2165T= c.1297T= (p.Phe433=) | dbSNP |