Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946111C>A | CA354704918 | FOXL2 | c.612G>T (p.Trp204Cys) | dbSNP gnomAD v4 |
3 | g.138946111C>T | CA10654879 | FOXL2 | c.612G>A (p.Trp204Ter) | ClinVar dbSNP gnomAD v4 |
3 | g.138946111C>G | CA354704923 | FOXL2 | c.612G>C (p.Trp204Cys) | dbSNP |