| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.189868627G>C | CA355755185 | TP63 | c.1040G>C (p.Cys347Ser) c.758G>C (p.Cys253Ser) c.503G>C (p.Cys168Ser) n.864G>C c.989G>C (p.Cys330Ser) c.1037G>C (p.Cys346Ser) c.1034G>C (p.Cys345Ser) c.1001G>C (p.Cys334Ser) | dbSNP |
| 3 | g.189868627G>T | CA16617858 | TP63 | c.1040G>T (p.Cys347Phe) c.758G>T (p.Cys253Phe) c.503G>T (p.Cys168Phe) n.864G>T c.989G>T (p.Cys330Phe) c.1037G>T (p.Cys346Phe) c.1034G>T (p.Cys345Phe) c.1001G>T (p.Cys334Phe) | ClinVar dbSNP |
| 3 | g.189868627G>A | CA355755184 | TP63 | c.1040G>A (p.Cys347Tyr) c.758G>A (p.Cys253Tyr) c.503G>A (p.Cys168Tyr) n.864G>A c.989G>A (p.Cys330Tyr) c.1037G>A (p.Cys346Tyr) c.1034G>A (p.Cys345Tyr) c.1001G>A (p.Cys334Tyr) | dbSNP |