| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.189808465G>T | CA355750729 | TP63 | c.518G>T (p.Gly173Val) c.236G>T (p.Gly79Val) c.42+18623G>T (n.42+18623G>T) n.342G>T c.467G>T (p.Gly156Val) c.515G>T (p.Gly172Val) c.512G>T (p.Gly171Val) c.479G>T (p.Gly160Val) | ClinVar dbSNP |
| 3 | g.189808465G>A | CA343283 | TP63 | c.518G>A (p.Gly173Asp) c.236G>A (p.Gly79Asp) c.42+18623G>A (n.42+18623G>A) n.342G>A c.467G>A (p.Gly156Asp) c.515G>A (p.Gly172Asp) c.512G>A (p.Gly171Asp) c.479G>A (p.Gly160Asp) | ClinVar dbSNP |
| 3 | g.189808465G>C | CA355750728 | TP63 | c.518G>C (p.Gly173Ala) c.236G>C (p.Gly79Ala) c.42+18623G>C (n.42+18623G>C) n.342G>C c.467G>C (p.Gly156Ala) c.515G>C (p.Gly172Ala) c.512G>C (p.Gly171Ala) c.479G>C (p.Gly160Ala) | dbSNP |