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Links from Gene

Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC1A2
(K489R +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GLikely benign
SLC1A2
(L381I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC1A2
Deletion
not provided
GUncertain significance
SLC1A2
(S525Y +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(V376fs +1 more)
Microsatellite
(frameshift variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(A70D +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(V538I +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(Q143H +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(R78K +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(G282V +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GLikely pathogenic
SLC1A2
(A284T +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(L38V +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
SLC1A2
(E194D +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 41
GUncertain significance
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