Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.87931078T>A | CA377481367 | PTEN | c.242T>A (p.Phe81Tyr) n.977T>A c.*72T>A (n.*72T>A) c.197T>A (p.Phe66Tyr) c.76T>A c.*277T>A (n.*277T>A) c.*353T>A (n.*353T>A) c.163T>A c.761T>A (p.Phe254Tyr) n.68T>A c.140T>A (p.Phe47Tyr) c.-509T>A (n.-509T>A) c.146T>A (p.Phe49Tyr) n.954T>A | ClinVar dbSNP |
10 | g.87931078T>G | CA10577417 | PTEN | c.242T>G (p.Phe81Cys) n.977T>G c.*72T>G (n.*72T>G) c.197T>G (p.Phe66Cys) c.76T>G c.*277T>G (n.*277T>G) c.*353T>G (n.*353T>G) c.163T>G c.761T>G (p.Phe254Cys) n.68T>G c.140T>G (p.Phe47Cys) c.-509T>G (n.-509T>G) c.146T>G (p.Phe49Cys) n.954T>G | ClinVar dbSNP COSMIC |