| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130060311, TTC19 (S67L) | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex III deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant) | Mitochondrial complex III deficiency nuclear type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | Mitochondrial complex III deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant) | Mitochondrial complex III deficiency nuclear type 2 | |
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