Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.22625484G>C	CA253847	FANCF	c.327C>G (p.Tyr109Ter)	ClinVar dbSNP
11	g.22625484G>A	CA473533715	FANCF	c.327C>T (p.Tyr109=)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11	g.22625484G=	CA1957581354	FANCF	c.327C= (p.Tyr109=)	dbSNP

Number of alleles fetched