| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.189808464G>C | CA16604496 | TP63 | c.517G>C (p.Gly173Arg) c.235G>C (p.Gly79Arg) c.42+18622G>C (n.42+18622G>C) n.341G>C c.466G>C (p.Gly156Arg) c.514G>C (p.Gly172Arg) c.511G>C (p.Gly171Arg) c.478G>C (p.Gly160Arg) | ClinVar dbSNP |
| 3 | g.189808464G>A | CA355750726 | TP63 | c.517G>A (p.Gly173Ser) c.235G>A (p.Gly79Ser) c.42+18622G>A (n.42+18622G>A) n.341G>A c.466G>A (p.Gly156Ser) c.514G>A (p.Gly172Ser) c.511G>A (p.Gly171Ser) c.478G>A (p.Gly160Ser) | ClinVar dbSNP |