| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42126660T>C | CA10264528 | CYP2D6 | c.1206A>G (n.1206A>G) c.1408A>G (p.Thr470Ala) c.1255A>G (p.Thr419Ala) c.1026A>G (n.1026A>G) c.1399A>G (p.Thr467Ala) n.2132A>G c.1264A>G (p.Thr422Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42126660T= | CA2406577846 | CYP2D6 | c.1206A= (n.1206A=) c.1408A= (p.Thr470=) c.1255A= (p.Thr419=) c.1026A= (n.1026A=) c.1399A= (p.Thr467=) n.2132A= c.1264A= (p.Thr422=) | dbSNP |