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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC113845788, CUL4B
Indel
(inframe_deletion)
not provided
GUncertain significance
CUL4B, LOC113845788
(T48A +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance