Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675071G>A | CA000257 | TP53 | c.541C>T (p.Arg181Cys) c.145C>T (p.Arg49Cys) c.262C>T (p.Arg88Cys) c.520C>T (p.Arg174Cys) n.797C>T n.49C>T c.424C>T (p.Arg142Cys) c.64C>T (p.Arg22Cys) c.508C>T (p.Arg170Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675071G>T | CA10580940 | TP53 | c.541C>A (p.Arg181Ser) c.145C>A (p.Arg49Ser) c.262C>A (p.Arg88Ser) c.520C>A (p.Arg174Ser) n.797C>A n.49C>A c.424C>A (p.Arg142Ser) c.64C>A (p.Arg22Ser) c.508C>A (p.Arg170Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |