Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675207G>A | CA497925728 | TP53 | c.405C>T (p.Cys135=) c.9C>T (p.Cys3=) c.126C>T (p.Cys42=) c.384C>T (p.Cys128=) n.661C>T c.288C>T (p.Cys96=) c.-73C>T (n.-73C>T) c.372C>T (p.Cys124=) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7675207G>C | CA16602987 | TP53 | c.405C>G (p.Cys135Trp) c.9C>G (p.Cys3Trp) c.126C>G (p.Cys42Trp) c.384C>G (p.Cys128Trp) n.661C>G c.288C>G (p.Cys96Trp) c.-73C>G (n.-73C>G) c.372C>G (p.Cys124Trp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675207G>T | CA397842771 | TP53 | c.405C>A (p.Cys135Ter) c.9C>A (p.Cys3Ter) c.126C>A (p.Cys42Ter) c.384C>A (p.Cys128Ter) n.661C>A c.288C>A (p.Cys96Ter) c.-73C>A (n.-73C>A) c.372C>A (p.Cys124Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |