| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.41965592G>A | CA342945 | GLI3 | c.3481C>T (p.Gln1161Ter) c.3307C>T (p.Gln1103Ter) n.3458C>T c.3304C>T (p.Gln1102Ter) c.3478C>T (p.Gln1160Ter) | ClinVar dbSNP |
| 7 | g.41965592G= | CA1702660837 | GLI3 | c.3481C= (p.Gln1161=) c.3307C= (p.Gln1103=) n.3458C= c.3304C= (p.Gln1102=) c.3478C= (p.Gln1160=) | dbSNP |