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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTAN1
(F46L +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
GUncertain significance
SPTAN1
(A570T +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
GUncertain significance
SPTAN1
(A961T +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 5
GLikely benign
SPTAN1
(E2072Q +4 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+2 more
GUncertain significance
SPTAN1
(E2207del +5 more)
Microsatellite
(inframe_deletion)
Developmental and epileptic encephalopathy, 5
+3 more
GPathogenic/Likely pathogenic
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