Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.138946068G>TCA354704507FOXL2c.655C>A (p.Gln219Lys)
 dbSNP gnomAD v4
3g.138946068G>CCA354704505FOXL2c.655C>G (p.Gln219Glu)
 dbSNP COSMIC
3g.138946068G>ACA210680FOXL2c.655C>T (p.Gln219Ter)
 ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched