U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(I1179V +1 more)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
+2 more
GConflicting classifications of pathogenicity
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
(I1045V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 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
SCN3A
(E527A)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
GUncertain significance
Format
Items per page
Sort by
Choose Destination