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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(M1825R +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
GLikely pathogenic
SCN3A
(L836F +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
GLikely pathogenic
SCN3A
(P679S +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
GUncertain significance
SCN3A
Single nucleotide variant
(splice donor variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
SCN3A
(L209P)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GLikely pathogenic
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