"Genome-Nilou Lab"[submitter] AND "FLVCR2"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95818	NM_017791.3(FLVCR2):c.47T>C (p.Val16Ala)	FLVCR2, FLVCR2-AS1 (V16A)	Single nucleotide variant (non-coding transcript variant +1 more)	Fowler syndrome +3 more	GBenign
Select item 95819	NM_017791.3(FLVCR2):c.543G>A (p.Val181=)	FLVCR2-AS1, FLVCR2	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GBenign
Select item 95820	NM_017791.3(FLVCR2):c.648C>G (p.Ser216=)	FLVCR2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign

Format

Sort by

Choose Destination

ClinVar