| | | Single nucleotide variant (intron variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (N403D +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (V645I +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (I425K +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (Q482K +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (K499N +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (A523T +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD-AS2, CYLD (K767* +3 more) | Single nucleotide variant (nonsense +1 more) | Familial cylindromatosis +2 more | |
| | CYLD, CYLD-AS2 (D579N +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (S584L +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (K587E +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (N596S +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (T822I +3 more) | Single nucleotide variant (missense variant +1 more) | Trichoepithelioma, multiple familial, 2 +3 more | |
| | CYLD, CYLD-AS2 (P603S +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (N607S +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (V613M +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (V613L +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (D621E +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (G627S +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD-AS2, CYLD (Q632L +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (E635Q +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (D657N +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (A659S +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |
| | CYLD, CYLD-AS2 (D668G +3 more) | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 | |