| | LOC130003514, OTUD1 (V157G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (P158Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (P174S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (P174L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (R191Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (A212E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (A230G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (R235K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (E238G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (P247S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (G248V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (R253P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (D256H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130003514, OTUD1 (P271S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |