| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Duplication | not provided | |
| | | Duplication | Proteasome-associated autoinflammatory syndrome 1 | |
| | LOC129996212, NUDT3 +1 more (A22G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RPS10-NUDT3, NUDT3 (I171F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
Click to view in NCBI Gene