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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC1A2
(R563H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC1A2
(V538I +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(S525Y +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(A400T +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
+1 more
GUncertain significance
SLC1A2
(V376fs +1 more)
Microsatellite
(frameshift variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(M259I +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
+1 more
GUncertain significance
SLC1A2
(S200N +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC1A2
(K148E +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
+1 more
GUncertain significance
SLC1A2
(Q143H +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(R106H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC1A2
(R78K +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(A70D +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
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