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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FCSK
(S223P)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation with defective fucosylation 2
GUncertain significance
FCSK
(A652V)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation with defective fucosylation 2
GUncertain significance
FCSK
(R683C)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation with defective fucosylation 2
+1 more
GConflicting classifications of pathogenicity
FCSK
(Y729C)
Single nucleotide variant
(missense variant)
Congenital disorder of glycosylation with defective fucosylation 2
GUncertain significance
FCSK
(R741*)
Single nucleotide variant
(nonsense)
Congenital disorder of glycosylation with defective fucosylation 2
GLikely pathogenic
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