| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946079T>A | CA354704605 | FOXL2 | c.644A>T (p.Tyr215Phe) | dbSNP |
| 3 | g.138946079T>C | CA10654876 | FOXL2 | c.644A>G (p.Tyr215Cys) | ClinVar dbSNP gnomAD v4 |
| 3 | g.138946079T>G | CA354704608 | FOXL2 | c.644A>C (p.Tyr215Ser) | dbSNP |