| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | Coenzyme Q10 deficiency, Spinocerebellar Ataxia Type +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive ataxia due to ubiquinone deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive cerebellar ataxia +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Coenzyme Q10 deficiency, Spinocerebellar Ataxia Type +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Coenzyme Q10 deficiency, Spinocerebellar Ataxia Type +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive ataxia due to ubiquinone deficiency +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive cerebellar ataxia +2 more | |
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