| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +1 more) | Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Deletion (frameshift variant +1 more) | Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Deletion (splice donor variant) | not provided +3 more | GPathogenic/Likely pathogenic |
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