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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COG5
(T372N +5 more)
Single nucleotide variant
(missense variant)
COG5-congenital disorder of glycosylation
+1 more
GUncertain significance
COG5
(R283*)
Single nucleotide variant
(nonsense +1 more)
COG5-congenital disorder of glycosylation
GPathogenic
COG5
(S247G)
Single nucleotide variant
(missense variant +1 more)
COG5-congenital disorder of glycosylation
GUncertain significance
COG5
(L206F)
Single nucleotide variant
(missense variant +1 more)
COG5-congenital disorder of glycosylation
GUncertain significance
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