| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936729, NDUFAF3 (Y11C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC129936729, NDUFAF3 (L17P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC129936729, NDUFAF3 (E23Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene