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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTAN1
(E13Q +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
GUncertain significance
SPTAN1
(C1910Y +4 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
GUncertain significance
SPTAN1
(A2148V +4 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
+1 more
GUncertain significance
SPTAN1
(R2308C +4 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GPathogenic/Likely pathogenic
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