Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
14	g.28767903C>G	CA123552	FOXG1	c.624C>G (p.Tyr208Ter)	ClinVar dbSNP
14	g.28767903C>A	CA389475504	FOXG1	c.624C>A (p.Tyr208Ter)	ClinVar dbSNP
14	g.28767903C>T	CA7140622	FOXG1	c.624C>T (p.Tyr208=)	ClinVar dbSNP ExAC gnomAD v2

Number of alleles fetched