| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7676056C>G | CA16615732 | TP53 | c.313G>C (p.Gly105Arg) c.-21-820G>C (n.-21-820G>C) c.96+326G>C (n.96+326G>C) n.569G>C c.196G>C (p.Gly66Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676056C>A | CA397844731 | TP53 | c.313G>T (p.Gly105Cys) c.-21-820G>T (n.-21-820G>T) c.96+326G>T (n.96+326G>T) n.569G>T c.196G>T (p.Gly66Cys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676056C>T | CA397844735 | TP53 | c.313G>A (p.Gly105Ser) c.-21-820G>A (n.-21-820G>A) c.96+326G>A (n.96+326G>A) n.569G>A c.196G>A (p.Gly66Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |