Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673810A>T | CA397837037 | TP53 | c.810T>A (p.Phe270Leu) c.414T>A (p.Phe138Leu) c.531T>A (p.Phe177Leu) c.789T>A (p.Phe263Leu) c.782+371T>A (n.782+371T>A) c.693T>A (p.Phe231Leu) c.333T>A (p.Phe111Leu) c.777T>A (p.Phe259Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673810A>C | CA16603017 | TP53 | c.810T>G (p.Phe270Leu) c.414T>G (p.Phe138Leu) c.531T>G (p.Phe177Leu) c.789T>G (p.Phe263Leu) c.782+371T>G (n.782+371T>G) c.693T>G (p.Phe231Leu) c.333T>G (p.Phe111Leu) c.777T>G (p.Phe259Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |