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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTNAP2
(W184*)
Single nucleotide variant
(nonsense)
Cortical dysplasia-focal epilepsy syndrome
GPathogenic
CNTNAP2
(N454fs)
Deletion
(frameshift variant)
Cortical dysplasia-focal epilepsy syndrome
GPathogenic/Likely pathogenic
CNTNAP2
(T648M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CNTNAP2
(R1088*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
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