| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946430C>T | CA10654896 | FOXL2 | c.293G>A (p.Trp98Ter) | ClinVar dbSNP |
| 3 | g.138946430C>A | CA354706969 | FOXL2 | c.293G>T (p.Trp98Leu) | dbSNP |
| 3 | g.138946430C>G | CA354706971 | FOXL2 | c.293G>C (p.Trp98Ser) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946430C>T | CA10654896 | FOXL2 | c.293G>A (p.Trp98Ter) | ClinVar dbSNP |
| 3 | g.138946430C>A | CA354706969 | FOXL2 | c.293G>T (p.Trp98Leu) | dbSNP |
| 3 | g.138946430C>G | CA354706971 | FOXL2 | c.293G>C (p.Trp98Ser) | dbSNP |