Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.138946566G>TCA354707739FOXL2c.157C>A (p.Gln53Lys)
 ClinVar dbSNP gnomAD v4 COSMIC
3g.138946566G>ACA210682FOXL2c.157C>T (p.Gln53Ter)
 ClinVar dbSNP
3g.138946566G=CA1405402570FOXL2c.157C= (p.Gln53=)
 dbSNP

Number of alleles fetched