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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKL5, RS1
(R197C)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic
CDKL5, RS1
(Y177*)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
CDKL5, RS1
(W163*)
Single nucleotide variant
(nonsense +1 more)
Juvenile retinoschisis
GLikely pathogenic
CDKL5, RS1
(S152fs)
Deletion
(frameshift variant +1 more)
Juvenile retinoschisis
GLikely pathogenic
CDKL5, RS1
Deletion
(intron variant +1 more)
Juvenile retinoschisis
GLikely pathogenic
CDKL5, RS1
(Q117*)
Single nucleotide variant
(nonsense +1 more)
Juvenile retinoschisis
GPathogenic
CDKL5, RS1
(R102Q)
Single nucleotide variant
(missense variant +1 more)
Juvenile retinoschisis
+3 more
GPathogenic
RS1
Single nucleotide variant
(splice donor variant)
Juvenile retinoschisis
+1 more
GPathogenic/Likely pathogenic
RS1
(G45fs)
Duplication
(frameshift variant)
Juvenile retinoschisis
GLikely pathogenic
RS1
(Y34*)
Duplication
(nonsense)
Juvenile retinoschisis
GLikely pathogenic
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