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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NGLY1
(C602Y +2 more)
Single nucleotide variant
(missense variant +1 more)
Congenital disorder of deglycosylation 1
GUncertain significance
NGLY1
(Q589fs +2 more)
Deletion
(frameshift variant +1 more)
Congenital disorder of deglycosylation
+2 more
GPathogenic
NGLY1
(D546fs +2 more)
Deletion
(frameshift variant +1 more)
Congenital disorder of deglycosylation 1
+1 more
GPathogenic/Likely pathogenic
NGLY1
(S448F +2 more)
Single nucleotide variant
(missense variant)
Congenital disorder of deglycosylation
+1 more
GUncertain significance
NGLY1
(V397L +2 more)
Single nucleotide variant
(missense variant)
Congenital disorder of deglycosylation 1
GUncertain significance
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