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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIITA
(G655fs +4 more)
Duplication
(frameshift variant +1 more)
MHC class II deficiency
GPathogenic/Likely pathogenic
CIITA
(H797R +4 more)
Single nucleotide variant
(missense variant +1 more)
MHC class II deficiency
GUncertain significance
CIITA
(Q316* +5 more)
Single nucleotide variant
(nonsense)
MHC class II deficiency
GLikely pathogenic
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