Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.53386097G>A | CA16044035 | DCC | c.2414G>A (p.Gly805Glu) c.2215G>A c.2345G>A (p.Gly782Glu) c.1379G>A (p.Gly460Glu) | ClinVar dbSNP |
18 | g.53386097G= | CA2304129495 | DCC | c.2414G= (p.Gly805=) c.2215G= c.2345G= (p.Gly782=) c.1379G= (p.Gly460=) | dbSNP |