Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7675160G>C | CA16603057 | TP53 | c.452C>G (p.Pro151Arg) c.56C>G (p.Pro19Arg) c.173C>G (p.Pro58Arg) c.431C>G (p.Pro144Arg) n.708C>G c.335C>G (p.Pro112Arg) c.-26C>G (n.-26C>G) c.419C>G (p.Pro140Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675160G>T | CA16603056 | TP53 | c.452C>A (p.Pro151His) c.56C>A (p.Pro19His) c.173C>A (p.Pro58His) c.431C>A (p.Pro144His) n.708C>A c.335C>A (p.Pro112His) c.-26C>A (n.-26C>A) c.419C>A (p.Pro140His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7675160G>A | CA397842213 | TP53 | c.452C>T (p.Pro151Leu) c.56C>T (p.Pro19Leu) c.173C>T (p.Pro58Leu) c.431C>T (p.Pro144Leu) n.708C>T c.335C>T (p.Pro112Leu) c.-26C>T (n.-26C>T) c.419C>T (p.Pro140Leu) | dbSNP COSMIC |