Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.124875581C>T | CA115393 | ROBO3 | c.2317C>T (p.Gln773Ter) c.2251C>T (p.Gln751Ter) c.3289C>T (p.Gln1097Ter) | ClinVar dbSNP |
11 | g.124875581C>G | CA383147659 | ROBO3 | c.2317C>G (p.Gln773Glu) c.2251C>G (p.Gln751Glu) c.3289C>G (p.Gln1097Glu) | dbSNP |