Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.12896000G>T | CA16041969 | GCDH | c.514G>T (p.Glu172Ter) n.492G>T n.879G>T c.478G>T (p.Glu160Ter) c.569G>T (p.Gly190Val) n.550G>T n.677G>T n.930G>T | ClinVar dbSNP COSMIC COSMIC COSMIC |
19 | g.12896000G= | CA2323623187 | GCDH | c.514G= (p.Glu172=) n.492G= n.879G= c.478G= (p.Glu160=) c.569G= (p.Gly190=) n.550G= n.677G= n.930G= | dbSNP |