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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL4B
(Q297fs +3 more)
Deletion
(frameshift variant)
X-linked intellectual disability Cabezas type
GLikely pathogenic
CUL4B
(I151T +3 more)
Single nucleotide variant
(missense variant)
X-linked intellectual disability Cabezas type
GUncertain significance