Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128321A>T | CA411773563 | CYP2D6 | c.543T>A (p.His181Gln) c.696T>A (p.His232Gln) c.363T>A (p.His121Gln) c.630T>A (p.His210Gln) n.1420T>A c.552T>A (p.His184Gln) | dbSNP |
22 | g.42128321A>G | CA10264905 | CYP2D6 | c.543T>C (p.His181=) c.696T>C (p.His232=) c.363T>C (p.His121=) c.630T>C (p.His210=) n.1420T>C c.552T>C (p.His184=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |