Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
17	g.8086169T>A	CA261174	ALOX12B	c.199A>T (p.Ile67Phe)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17	g.8086169T>C	CA397999923	ALOX12B	c.199A>G (p.Ile67Val)	dbSNP gnomAD v4
17	g.8086169T=	CA2246104835	ALOX12B	c.199A= (p.Ile67=)	dbSNP

Number of alleles fetched