| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Familial cold autoinflammatory syndrome 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cold autoinflammatory syndrome 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Familial cold autoinflammatory syndrome 2 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Familial cold autoinflammatory syndrome 2 | |
| | | Insertion (splice donor variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autoinflammatory syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autoinflammatory syndrome +2 more | |
| | | Single nucleotide variant (nonsense) | Familial cold autoinflammatory syndrome 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autoinflammatory syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Autoinflammatory syndrome +2 more | |
Click to view in NCBI Gene