| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice acceptor variant) | Combined oxidative phosphorylation defect type 27 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +2 more) | Combined oxidative phosphorylation defect type 27 | |
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