Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.41966069del | CA342939 | GLI3 | c.3004del (p.Val1002Ter) c.2830del (p.Val944Ter) n.2981del c.2827del (p.Val943Ter) c.3001del (p.Val1001Ter) | dbSNP |
7 | g.41966069C= | CA1702661093 | GLI3 | c.3004G= (p.Val1002=) c.2830G= (p.Val944=) n.2981G= c.2827G= (p.Val943=) c.3001G= (p.Val1001=) | dbSNP dbSNP |