| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | COG5-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +1 more) | COG5-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | COG5-congenital disorder of glycosylation +2 more | |
| | | Duplication (intron variant) | COG5-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +1 more) | COG5-congenital disorder of glycosylation +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | COG5-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | COG5-congenital disorder of glycosylation +2 more | |
| | | Duplication (intron variant) | not provided +1 more | |
| | | Deletion (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | COG5-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +1 more) | COG5-congenital disorder of glycosylation | GPathogenic/Likely pathogenic |
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