Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
10	g.102504196C>T	CA116361	SUFU	c.44C>T (p.Pro15Leu) c.8+1210C>T (n.8+1210C>T)	ClinVar dbSNP
10	g.102504196C=	CA1932719258	SUFU	c.44C= (p.Pro15=) c.8+1210C= (n.8+1210C=)	dbSNP

Number of alleles fetched