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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL3
(I675T +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CUL3
(E581* +2 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
CUL3
Deletion
(intron variant)
not provided
GUncertain significance
CUL3
(M207V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL3
Single nucleotide variant
(intron variant +1 more)
not provided
GLikely pathogenic
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