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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKL5
(S196L)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 2
+4 more
GPathogenic/Likely pathogenic
CDKL5
(E416fs)
Microsatellite
(frameshift variant)
CDKL5 disorder
GPathogenic
CDKL5
(K485fs)
Duplication
(frameshift variant)
Epileptic encephalopathy
GPathogenic
CDKL5
(Q881*)
Single nucleotide variant
(nonsense)
Focal epilepsy
GPathogenic
CDKL5, RS1
(G994R)
Single nucleotide variant
(missense variant +1 more)
CDKL5 disorder
GLikely benign
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