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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCC
(K419fs)
Deletion
(frameshift variant)
Mirror movements 1
GLikely pathogenic
DCC, MIR4528
Copy number loss
Mirror movements 1
GUncertain significance
DCC
(Y768*)
Single nucleotide variant
(nonsense)
Mirror movements 1
GLikely pathogenic
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