| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7676037A>T | CA16603051 | TP53 | c.332T>A (p.Leu111Gln) c.-21-801T>A (n.-21-801T>A) c.96+345T>A (n.96+345T>A) n.588T>A c.215T>A (p.Leu72Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676037A>G | CA16603049 | TP53 | c.332T>C (p.Leu111Pro) c.-21-801T>C (n.-21-801T>C) c.96+345T>C (n.96+345T>C) n.588T>C c.215T>C (p.Leu72Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7676037A>C | CA16603050 | TP53 | c.332T>G (p.Leu111Arg) c.-21-801T>G (n.-21-801T>G) c.96+345T>G (n.96+345T>G) n.588T>G c.215T>G (p.Leu72Arg) | ClinVar dbSNP |
| 17 | g.7676037A= | CA2245933118 | TP53 | c.332T= (p.Leu111=) c.-21-801T= (n.-21-801T=) c.96+345T= (n.96+345T=) n.588T= c.215T= (p.Leu72=) | dbSNP |