"Blueprint Genetics"[submitter] AND "RAG2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36717	NM_000536.4(RAG2):c.1247G>T (p.Trp416Leu)	RAG2 (W416L)	Single nucleotide variant (missense variant)	Recombinase activating gene 2 deficiency	GLikely pathogenic FDA Recognized database
Select item 636599	NM_000536.4(RAG2):c.273C>A (p.Tyr91Ter)	RAG2 (Y91*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic