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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRAT1
(T787M +2 more)
Single nucleotide variant
(missense variant +1 more)
Neonatal-onset encephalopathy with rigidity and seizures
+2 more
GConflicting classifications of pathogenicity
BRAT1
(R427Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Neonatal-onset encephalopathy with rigidity and seizures
+2 more
GConflicting classifications of pathogenicity
BRAT1
(W232* +1 more)
Single nucleotide variant
(nonsense +1 more)
Neonatal-onset encephalopathy with rigidity and seizures
GPathogenic
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