Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.189868639A>T | CA355755209 | TP63 | c.1052A>T (p.Asp351Val) c.770A>T (p.Asp257Val) c.515A>T (p.Asp172Val) n.876A>T c.1001A>T (p.Asp334Val) c.1049A>T (p.Asp350Val) c.1046A>T (p.Asp349Val) c.1013A>T (p.Asp338Val) | dbSNP |
3 | g.189868639A>G | CA118341 | TP63 | c.1052A>G (p.Asp351Gly) c.770A>G (p.Asp257Gly) c.515A>G (p.Asp172Gly) n.876A>G c.1001A>G (p.Asp334Gly) c.1049A>G (p.Asp350Gly) c.1046A>G (p.Asp349Gly) c.1013A>G (p.Asp338Gly) | ClinVar dbSNP |