| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +2 more) | Mitochondrial complex 1 deficiency, nuclear type 16 +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Mitochondrial complex 1 deficiency, nuclear type 16 +1 more | |
| | | Single nucleotide variant (intron variant) | Mitochondrial complex 1 deficiency, nuclear type 16 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
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