| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CYLD, CYLD-AS2 (P803L +3 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CYLD-AS2, CYLD (S414L +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CYLD, CYLD-AS2 (D879E +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CYLD, CYLD-AS2 (Q945H +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene