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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COG4
(E614* +2 more)
Single nucleotide variant
(nonsense +1 more)
COG4-congenital disorder of glycosylation
+2 more
GPathogenic
COG4
Single nucleotide variant
(intron variant)
COG4-congenital disorder of glycosylation
+3 more
GBenign/Likely benign
COG4
(I129V +2 more)
Single nucleotide variant
(missense variant +1 more)
COG4-congenital disorder of glycosylation
+1 more
GLikely benign
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