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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL4B
(R624W +3 more)
Single nucleotide variant
(missense variant)
X-linked intellectual disability Cabezas type
GUncertain significance
CUL4B
(L434P +3 more)
Single nucleotide variant
(missense variant)
X-linked intellectual disability Cabezas type
GUncertain significance
CUL4B
(I318fs +3 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
CUL4B, LOC113845788
(Q18R +2 more)
Single nucleotide variant
(missense variant)
X-linked intellectual disability Cabezas type
GConflicting classifications of pathogenicity
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