Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.41972378C>A | CA342916 | GLI3 | c.2062G>T (p.Glu688Ter) c.1888G>T (p.Glu630Ter) n.2039G>T c.1885G>T (p.Glu629Ter) c.2059G>T (p.Glu687Ter) | dbSNP |
7 | g.41972378C>T | CA367321903 | GLI3 | c.2062G>A (p.Glu688Lys) c.1888G>A (p.Glu630Lys) n.2039G>A c.1885G>A (p.Glu629Lys) c.2059G>A (p.Glu687Lys) | dbSNP |
7 | g.41972378C= | CA1702647682 | GLI3 | c.2062G= (p.Glu688=) c.1888G= (p.Glu630=) n.2039G= c.1885G= (p.Glu629=) c.2059G= (p.Glu687=) | dbSNP |