Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.138946428G>A	CA210688	FOXL2	c.295C>T (p.Gln99Ter)	ClinVar dbSNP
3	g.138946428G>T	CA2639784	FOXL2	c.295C>A (p.Gln99Lys)	dbSNP ExAC gnomAD v2 gnomAD v4
3	g.138946428G>C	CA354706960	FOXL2	c.295C>G (p.Gln99Glu)	dbSNP

Number of alleles fetched