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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC13A5
(V471A +2 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 25
GUncertain significance
SLC13A5
(I483V +2 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 25
GUncertain significance
SLC13A5
(R380C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
SLC13A5
(R333* +2 more)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 25
+2 more
GPathogenic/Likely pathogenic
SLC13A5
(G219R +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 25
+2 more
GPathogenic/Likely pathogenic
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