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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MLC1
(L227Q +5 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
MLC1
(V224fs +5 more)
Deletion
(frameshift variant +1 more)
Megalencephalic leukoencephalopathy with subcortical cysts 1
GPathogenic
MLC1
(G212R +4 more)
Single nucleotide variant
(missense variant +1 more)
Megalencephalic leukoencephalopathy with subcortical cysts 1
+2 more
GPathogenic/Likely pathogenic
MLC1
(A130D +4 more)
Single nucleotide variant
(missense variant +1 more)
Megalencephalic leukoencephalopathy with subcortical cysts 1
GUncertain significance
MLC1
(V17L +2 more)
Single nucleotide variant
(missense variant +2 more)
Megalencephalic leukoencephalopathy with subcortical cysts 1
GUncertain significance
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