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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DEPDC5
(V100M)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GUncertain significance
DEPDC5
(E770V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DEPDC5
(C1053F +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GUncertain significance
DEPDC5
(S1104L +3 more)
Single nucleotide variant
(missense variant +2 more)
Familial focal epilepsy with variable foci
+4 more
GConflicting classifications of pathogenicity
DEPDC5
(W1269* +6 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
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