Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946024_138946050del | CA899582492 | FOXL2 | c.677_703del (p.Ala226_Ala234del) | dbSNP |
3 | g.138946021_138946050dup | CA10654869 | FOXL2 | c.674_703dup (p.Ala234_Gly235insAlaAlaAlaAlaAlaAlaAlaAlaAlaAla) | ClinVar dbSNP |