| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7676011T>G | CA16620634 | TP53 | c.358A>C (p.Lys120Gln) c.-21-775A>C (n.-21-775A>C) c.96+371A>C (n.96+371A>C) n.614A>C c.241A>C (p.Lys81Gln) c.340+14A>C (n.340+14A>C) | ClinVar dbSNP COSMIC |
| 17 | g.7676011T>C | CA000130 | TP53 | c.358A>G (p.Lys120Glu) c.-21-775A>G (n.-21-775A>G) c.96+371A>G (n.96+371A>G) n.614A>G c.241A>G (p.Lys81Glu) c.340+14A>G (n.340+14A>G) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676011T>A | CA000132 | TP53 | c.358A>T (p.Lys120Ter) c.-21-775A>T (n.-21-775A>T) c.96+371A>T (n.96+371A>T) n.614A>T c.241A>T (p.Lys81Ter) c.340+14A>T (n.340+14A>T) | ClinVar dbSNP gnomAD v4 COSMIC |