| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996857, NDUFAF4 (M25T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996857, NDUFAF4 (R20Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene