Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42129779A>C | CA411775041 | CYP2D6 | c.311T>G (p.Val104Gly) c.131T>G (p.Val44Gly) c.245T>G (p.Val82Gly) n.1035T>G c.168T>G (p.Cys56Trp) | dbSNP |
22 | g.42129779A>T | CA10265255 | CYP2D6 | c.311T>A (p.Val104Glu) c.131T>A (p.Val44Glu) c.245T>A (p.Val82Glu) n.1035T>A c.168T>A (p.Cys56Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42129779A>G | CA10265254 | CYP2D6 | c.311T>C (p.Val104Ala) c.131T>C (p.Val44Ala) c.245T>C (p.Val82Ala) n.1035T>C c.168T>C (p.Cys56=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |