| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42129819G>A | CA514700903 | CYP2D6 | c.271C>T (p.Leu91=) c.91C>T (p.Leu31=) c.205C>T (p.Leu69=) n.995C>T c.128C>T (p.Ala43Val) | dbSNP |
| 22 | g.42129819G>C | CA411775204 | CYP2D6 | c.271C>G (p.Leu91Val) c.91C>G (p.Leu31Val) c.205C>G (p.Leu69Val) n.995C>G c.128C>G (p.Ala43Gly) | dbSNP gnomAD v4 |
| 22 | g.42129819G>T | CA10265278 | CYP2D6 | c.271C>A (p.Leu91Met) c.91C>A (p.Leu31Met) c.205C>A (p.Leu69Met) n.995C>A c.128C>A (p.Ala43Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |