| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42126623G>C | CA324664505 | CYP2D6 | c.1243C>G (n.1243C>G) c.1445C>G (p.Ala482Gly) c.1292C>G (p.Ala431Gly) c.1063C>G (n.1063C>G) c.1436C>G (p.Ala479Gly) n.2169C>G c.1301C>G (p.Ala434Gly) | dbSNP |
| 22 | g.42126623G= | CA2406577818 | CYP2D6 | c.1243C= (n.1243C=) c.1445C= (p.Ala482=) c.1292C= (p.Ala431=) c.1063C= (n.1063C=) c.1436C= (p.Ala479=) n.2169C= c.1301C= (p.Ala434=) | dbSNP |