| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7673799A>G | CA16603091 | TP53 | c.821T>C (p.Val274Ala) c.425T>C (p.Val142Ala) c.542T>C (p.Val181Ala) c.800T>C (p.Val267Ala) c.782+382T>C (n.782+382T>C) c.704T>C (p.Val235Ala) c.344T>C (p.Val115Ala) c.788T>C (p.Val263Ala) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673799A>C | CA16603090 | TP53 | c.821T>G (p.Val274Gly) c.425T>G (p.Val142Gly) c.542T>G (p.Val181Gly) c.800T>G (p.Val267Gly) c.782+382T>G (n.782+382T>G) c.704T>G (p.Val235Gly) c.344T>G (p.Val115Gly) c.788T>G (p.Val263Gly) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7673799A>T | CA16603089 | TP53 | c.821T>A (p.Val274Asp) c.425T>A (p.Val142Asp) c.542T>A (p.Val181Asp) c.800T>A (p.Val267Asp) c.782+382T>A (n.782+382T>A) c.704T>A (p.Val235Asp) c.344T>A (p.Val115Asp) c.788T>A (p.Val263Asp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |