| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive spinocerebellar ataxia 10 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive spinocerebellar ataxia 10 | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Autosomal recessive spinocerebellar ataxia 10 | |
| | | Duplication (frameshift variant) | Autosomal recessive cerebellar ataxia +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Autosomal recessive spinocerebellar ataxia 10 +1 more | |
Click to view in NCBI Gene