| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42127503C>A | CA411771460 | CYP2D6 | c.915G>T (n.915G>T) c.1117G>T (p.Gly373Cys) c.964G>T (p.Gly322Cys) c.735G>T (n.735G>T) c.1108G>T (p.Gly370Cys) n.1841G>T c.973G>T (p.Gly325Cys) | dbSNP gnomAD v4 |
| 22 | g.42127503C>T | CA10264639 | CYP2D6 | c.915G>A (n.915G>A) c.1117G>A (p.Gly373Ser) c.964G>A (p.Gly322Ser) c.735G>A (n.735G>A) c.1108G>A (p.Gly370Ser) n.1841G>A c.973G>A (p.Gly325Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.42127503C= | CA2406578473 | CYP2D6 | c.915G= (n.915G=) c.1117G= (p.Gly373=) c.964G= (p.Gly322=) c.735G= (n.735G=) c.1108G= (p.Gly370=) n.1841G= c.973G= (p.Gly325=) | dbSNP |