| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.42127611C>T | CA10264689 | CYP2D6 | c.807G>A (n.807G>A) c.1009G>A (p.Asp337Asn) c.856G>A (p.Asp286Asn) c.627G>A (n.627G>A) c.1000G>A (p.Asp334Asn) n.1733G>A c.865G>A (p.Asp289Asn) c.867G>A (p.Thr289=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 22 | g.42127611C>A | CA411771920 | CYP2D6 | c.807G>T (n.807G>T) c.1009G>T (p.Asp337Tyr) c.856G>T (p.Asp286Tyr) c.627G>T (n.627G>T) c.1000G>T (p.Asp334Tyr) n.1733G>T c.865G>T (p.Asp289Tyr) c.867G>T (p.Thr289=) | dbSNP |
| 22 | g.42127611C= | CA2406578557 | CYP2D6 | c.807G= (n.807G=) c.1009G= (p.Asp337=) c.856G= (p.Asp286=) c.627G= (n.627G=) c.1000G= (p.Asp334=) n.1733G= c.865G= (p.Asp289=) c.867G= (p.Thr289=) | dbSNP |