| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946068G>T | CA354704507 | FOXL2 | c.655C>A (p.Gln219Lys) | dbSNP gnomAD v4 |
| 3 | g.138946068G>C | CA354704505 | FOXL2 | c.655C>G (p.Gln219Glu) | dbSNP COSMIC |
| 3 | g.138946068G>A | CA210680 | FOXL2 | c.655C>T (p.Gln219Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 3 | g.138946068G= | CA1405402329 | FOXL2 | c.655C= (p.Gln219=) | dbSNP |