Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128897C>A | CA411774003 | CYP2D6 | c.400G>T (p.Val134Leu) c.553G>T (p.Val185Leu) c.220G>T (p.Val74Leu) c.487G>T (p.Val163Leu) n.1277G>T c.409G>T (p.Val137Leu) | dbSNP |
22 | g.42128897C>G | CA10265038 | CYP2D6 | c.400G>C (p.Val134Leu) c.553G>C (p.Val185Leu) c.220G>C (p.Val74Leu) c.487G>C (p.Val163Leu) n.1277G>C c.409G>C (p.Val137Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128897C>T | CA411774004 | CYP2D6 | c.400G>A (p.Val134Met) c.553G>A (p.Val185Met) c.220G>A (p.Val74Met) c.487G>A (p.Val163Met) n.1277G>A c.409G>A (p.Val137Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |