| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42127608C>T | CA10264686 | CYP2D6 | c.810G>A (n.810G>A) c.1012G>A (p.Val338Met) c.859G>A (p.Val287Met) c.630G>A (n.630G>A) c.1003G>A (p.Val335Met) n.1736G>A c.868G>A (p.Val290Met) c.870G>A (p.Thr290=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42127608C>A | CA411771903 | CYP2D6 | c.810G>T (n.810G>T) c.1012G>T (p.Val338Leu) c.859G>T (p.Val287Leu) c.630G>T (n.630G>T) c.1003G>T (p.Val335Leu) n.1736G>T c.868G>T (p.Val290Leu) c.870G>T (p.Thr290=) | dbSNP |