| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Deletion (frameshift variant) | Hereditary spastic paraplegia 35 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 35 | |
| | | Single nucleotide variant (missense variant +1 more) | Spastic paraplegia +1 more | |
Click to view in NCBI Gene