| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.136200737del | CA250569 | LHX3 | c.111del (p.Gly38AlafsTer?) c.96del (p.Gly33AlafsTer?) n.220del c.63del (p.Gly22AlafsTer?) c.24del (p.Gly9AlafsTer?) | ClinVar dbSNP |
| 9 | g.136200737A= | CA3165530932 | LHX3 | c.111T= (p.Ala37=) c.96T= (p.Ala32=) n.220T= c.63T= (p.Ala21=) c.24T= (p.Ala8=) | dbSNP dbSNP |