| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42128181A>T | CA10264852 | CYP2D6 | c.683T>A (p.Met228Lys) c.836T>A (p.Met279Lys) c.503T>A (p.Met168Lys) c.770T>A (p.Met257Lys) n.1560T>A c.692T>A (p.Met231Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42128181A>C | CA411773017 | CYP2D6 | c.683T>G (p.Met228Arg) c.836T>G (p.Met279Arg) c.503T>G (p.Met168Arg) c.770T>G (p.Met257Arg) n.1560T>G c.692T>G (p.Met231Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 22 | g.42128181A>G | CA411773020 | CYP2D6 | c.683T>C (p.Met228Thr) c.836T>C (p.Met279Thr) c.503T>C (p.Met168Thr) c.770T>C (p.Met257Thr) n.1560T>C c.692T>C (p.Met231Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 22 | g.42128181A= | CA2406578983 | CYP2D6 | c.683T= (p.Met228=) c.836T= (p.Met279=) c.503T= (p.Met168=) c.770T= (p.Met257=) n.1560T= c.692T= (p.Met231=) | dbSNP |