Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674249A>T | CA397839181 | TP53 | c.714T>A (p.Cys238Ter) c.318T>A (p.Cys106Ter) c.435T>A (p.Cys145Ter) c.693T>A (p.Cys231Ter) c.597T>A (p.Cys199Ter) c.237T>A (p.Cys79Ter) c.681T>A (p.Cys227Ter) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674249A>G | CA497717529 | TP53 | c.714T>C (p.Cys238=) c.318T>C (p.Cys106=) c.435T>C (p.Cys145=) c.693T>C (p.Cys231=) c.597T>C (p.Cys199=) c.237T>C (p.Cys79=) c.681T>C (p.Cys227=) | dbSNP COSMIC |
17 | g.7674249A>C | CA000353 | TP53 | c.714T>G (p.Cys238Trp) c.318T>G (p.Cys106Trp) c.435T>G (p.Cys145Trp) c.693T>G (p.Cys231Trp) c.597T>G (p.Cys199Trp) c.237T>G (p.Cys79Trp) c.681T>G (p.Cys227Trp) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |