| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.58976421T>G | CA128852 | PDE4D | c.1567A>C (p.Thr523Pro) c.1759A>C (p.Thr587Pro) c.1429A>C (p.Thr477Pro) c.1611A>C (n.1611A>C) c.886A>C (p.Thr296Pro) c.853A>C (p.Thr285Pro) c.1351A>C (p.Thr451Pro) c.1393A>C (p.Thr465Pro) c.1576A>C (p.Thr526Pro) c.1369A>C (p.Thr457Pro) n.1495A>C c.1366A>C (p.Thr456Pro) c.1087A>C (p.Thr363Pro) c.1723A>C (p.Thr575Pro) c.1546A>C (p.Thr516Pro) c.1339A>C (p.Thr447Pro) c.1318A>C (p.Thr440Pro) c.1255A>C (p.Thr419Pro) c.991A>C (p.Thr331Pro) c.1561A>C (p.Thr521Pro) | ClinVar dbSNP |
| 5 | g.58976421T= | CA1549122359 | PDE4D | c.1567A= (p.Thr523=) c.1759A= (p.Thr587=) c.1429A= (p.Thr477=) c.1611A= (n.1611A=) c.886A= (p.Thr296=) c.853A= (p.Thr285=) c.1351A= (p.Thr451=) c.1393A= (p.Thr465=) c.1576A= (p.Thr526=) c.1369A= (p.Thr457=) n.1495A= c.1366A= (p.Thr456=) c.1087A= (p.Thr363=) c.1723A= (p.Thr575=) c.1546A= (p.Thr516=) c.1339A= (p.Thr447=) c.1318A= (p.Thr440=) c.1255A= (p.Thr419=) c.991A= (p.Thr331=) c.1561A= (p.Thr521=) | dbSNP |