Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946518C>T | CA210812 | FOXL2 | c.205G>A (p.Glu69Lys) | ClinVar dbSNP |
3 | g.138946518C>G | CA354707350 | FOXL2 | c.205G>C (p.Glu69Gln) | dbSNP |
3 | g.138946518C>A | CA10654901 | FOXL2 | c.205G>T (p.Glu69Ter) | ClinVar dbSNP |