| | LOC126859938, USP42 (K474Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (G486R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (K521R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (R533G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (L546S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (N548K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (V553I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (S556C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (T571M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (P581L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (V603M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (E617K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (T630M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (P669L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (P676S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (N697D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859938, USP42 (T730M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |