| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946163C>G | CA354705479 | FOXL2 | c.560G>C (p.Gly187Ala) | dbSNP |
| 3 | g.138946163C>T | CA117109 | FOXL2 | c.560G>A (p.Gly187Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.138946163C>A | CA354705480 | FOXL2 | c.560G>T (p.Gly187Val) | dbSNP |