Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42128933G>C | CA411774122 | CYP2D6 | c.364C>G (p.Arg122Gly) c.517C>G (p.Arg173Gly) c.184C>G (p.Arg62Gly) c.451C>G (p.Arg151Gly) n.1241C>G c.373C>G (p.Arg125Gly) | dbSNP |
22 | g.42128933G>A | CA10265054 | CYP2D6 | c.364C>T (p.Arg122Cys) c.517C>T (p.Arg173Cys) c.184C>T (p.Arg62Cys) c.451C>T (p.Arg151Cys) n.1241C>T c.373C>T (p.Arg125Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42128933G= | CA2406579584 | CYP2D6 | c.364C= (p.Arg122=) c.517C= (p.Arg173=) c.184C= (p.Arg62=) c.451C= (p.Arg151=) n.1241C= c.373C= (p.Arg125=) | dbSNP |