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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAG1
(R142*)
Single nucleotide variant
(nonsense)
Recombinase activating gene 1 deficiency
GPathogenic
RAG1
(C363Y)
Single nucleotide variant
(missense variant)
Recombinase activating gene 1 deficiency
GUncertain significance
RAG1
(R410Q)
Single nucleotide variant
(missense variant)
Combined immunodeficiency with skin granulomas
+2 more
GPathogenic/Likely pathogenic
RAG2
(C446W)
Single nucleotide variant
(missense variant)
Recombinase activating gene 2 deficiency
GLikely pathogenic
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