| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7675124T>G | CA397841928 | TP53 | c.488A>C (p.Tyr163Ser) c.92A>C (p.Tyr31Ser) c.209A>C (p.Tyr70Ser) c.467A>C (p.Tyr156Ser) n.744A>C c.371A>C (p.Tyr124Ser) c.11A>C (p.Tyr4Ser) c.455A>C (p.Tyr152Ser) | dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
| 17 | g.7675124T>C | CA000240 | TP53 | c.488A>G (p.Tyr163Cys) c.92A>G (p.Tyr31Cys) c.209A>G (p.Tyr70Cys) c.467A>G (p.Tyr156Cys) n.744A>G c.371A>G (p.Tyr124Cys) c.11A>G (p.Tyr4Cys) c.455A>G (p.Tyr152Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |