| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42128815C>G | CA411773820 | CYP2D6 | c.482G>C (p.Gly161Ala) c.635G>C (p.Gly212Ala) c.302G>C (p.Gly101Ala) c.569G>C (p.Gly190Ala) n.1359G>C c.491G>C (p.Gly164Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42128815C>T | CA10264996 | CYP2D6 | c.482G>A (p.Gly161Glu) c.635G>A (p.Gly212Glu) c.302G>A (p.Gly101Glu) c.569G>A (p.Gly190Glu) n.1359G>A c.491G>A (p.Gly164Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42128815C= | CA2406579494 | CYP2D6 | c.482G= (p.Gly161=) c.635G= (p.Gly212=) c.302G= (p.Gly101=) c.569G= (p.Gly190=) n.1359G= c.491G= (p.Gly164=) | dbSNP |