| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936730, NDUFAF3 (A37T) | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex I deficiency, nuclear type 1 +1 more | |
| | LOC129936730, NDUFAF3 (D38N) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Duplication (nonsense) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Copy number gain | not provided | |
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