Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.124871062G>C | CA383139601 | ROBO3 | c.1082G>C (p.Gly361Ala) c.1016G>C (p.Gly339Ala) c.2054G>C (p.Gly685Ala) | dbSNP |
11 | g.124871062G>A | CA115383 | ROBO3 | c.1082G>A (p.Gly361Glu) c.1016G>A (p.Gly339Glu) c.2054G>A (p.Gly685Glu) | ClinVar dbSNP |