| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130058651, USP31 (P106A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130058651, USP31 (G97V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130058651, USP31 (P96R) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC130058651, USP31 (P95R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene