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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCL9
(P113S)
Single nucleotide variant
(missense variant)
BCL9-related disorder
GLikely benign
BCL9
(G302D)
Single nucleotide variant
(missense variant)
BCL9-related disorder
+1 more
GLikely benign
BCL9
(M568del)
Deletion
(inframe deletion)
BCL9-related disorder
GLikely benign
BCL9
(R1064*)
Single nucleotide variant
(nonsense)
BCL9-related disorder
GUncertain significance
BCL9
(L1183V)
Single nucleotide variant
(missense variant)
BCL9-related disorder
GLikely benign
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