| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.41966274G>C | CA342936 | GLI3 | c.2799C>G (p.Tyr933Ter) c.2625C>G (p.Tyr875Ter) n.2776C>G c.2622C>G (p.Tyr874Ter) c.2796C>G (p.Tyr932Ter) | dbSNP |
| 7 | g.41966274G>A | CA454662354 | GLI3 | c.2799C>T (p.Tyr933=) c.2625C>T (p.Tyr875=) n.2776C>T c.2622C>T (p.Tyr874=) c.2796C>T (p.Tyr932=) | dbSNP gnomAD v4 COSMIC |
| 7 | g.41966274G= | CA1702661214 | GLI3 | c.2799C= (p.Tyr933=) c.2625C= (p.Tyr875=) n.2776C= c.2622C= (p.Tyr874=) c.2796C= (p.Tyr932=) | dbSNP |