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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(T1547M +1 more)
Single nucleotide variant
(missense variant)
Epilepsy, familial focal, with variable foci 4
+2 more
GUncertain significance
SCN3A
(V1347M +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SCN3A
Single nucleotide variant
(intron variant)
not provided
+2 more
GUncertain significance
SCN3A
(P555T)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
+1 more
GUncertain significance
SCN3A
Single nucleotide variant
(intron variant)
Developmental and epileptic encephalopathy, 62
+1 more
GUncertain significance
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