| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.41967917G>A | CA342918 | GLI3 | c.2110C>T (p.Gln704Ter) c.1936C>T (p.Gln646Ter) n.2087C>T c.1933C>T (p.Gln645Ter) c.2107C>T (p.Gln703Ter) | ClinVar dbSNP |
| 7 | g.41967917G= | CA1702661970 | GLI3 | c.2110C= (p.Gln704=) c.1936C= (p.Gln646=) n.2087C= c.1933C= (p.Gln645=) c.2107C= (p.Gln703=) | dbSNP |