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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DEPDC5
(V438fs +1 more)
Duplication
(frameshift variant +1 more)
Epilepsy, familial focal, with variable foci 1
GLikely pathogenic
DEPDC5
(P806A +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
DEPDC5
Single nucleotide variant
(intron variant)
Epilepsy, familial focal, with variable foci 1
GUncertain significance
DEPDC5
(Y1222C +6 more)
Single nucleotide variant
(missense variant +1 more)
Familial focal epilepsy with variable foci
+1 more
GUncertain significance
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