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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPLX1
(L128M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CPLX1
(E108*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 63
+1 more
GLikely pathogenic
CPLX1
(C105*)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 63
GPathogenic/Likely pathogenic
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