Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7676044A>C | CA16608667 | TP53 | c.325T>G (p.Phe109Val) c.-21-808T>G (n.-21-808T>G) c.96+338T>G (n.96+338T>G) n.581T>G c.208T>G (p.Phe70Val) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7676044A>T | CA397844614 | TP53 | c.325T>A (p.Phe109Ile) c.-21-808T>A (n.-21-808T>A) c.96+338T>A (n.96+338T>A) n.581T>A c.208T>A (p.Phe70Ile) | ClinVar dbSNP |