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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(T1161I +1 more)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
+2 more
GUncertain significance
SCN3A
(A1167T +1 more)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
+2 more
GUncertain significance
SCN3A
(S1078G +1 more)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
+2 more
GUncertain significance
SCN3A
(I875T +1 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
GPathogenic
SCN3A
(M777L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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