| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | |
| | | Deletion (frameshift variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive ataxia due to ubiquinone deficiency +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive ataxia due to ubiquinone deficiency +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene