| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.136198755C>T | CA250572 | LHX3 | c.687G>A (p.Trp229Ter) c.672G>A (p.Trp224Ter) n.1497G>A c.639G>A (p.Trp213Ter) c.600G>A (p.Trp200Ter) | ClinVar dbSNP |
| 9 | g.136198755C= | CA1884105883 | LHX3 | c.687G= (p.Trp229=) c.672G= (p.Trp224=) n.1497G= c.639G= (p.Trp213=) c.600G= (p.Trp200=) | dbSNP |