Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.10142179G>T	CA357019	VHL	c.332G>T (p.Ser111Ile)	ClinVar dbSNP COSMIC
3	g.10142179G>C	CA351751328	VHL	c.332G>C (p.Ser111Thr)	dbSNP
3	g.10142179G>A	CA357091	VHL	c.332G>A (p.Ser111Asn)	ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched