| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Huntington disease-like 1 +6 more | |
| | | Microsatellite (inframe_deletion) | Fatal familial insomnia +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Gerstmann-Straussler-Scheinker syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Huntington disease-like 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Spongiform encephalopathy with neuropsychiatric features +6 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance |
| | | Single nucleotide variant (missense variant +1 more) | Huntington disease-like 1 +6 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance |
| | | Single nucleotide variant (synonymous variant +1 more) | Huntington disease-like 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Spongiform encephalopathy with neuropsychiatric features +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Kuru, susceptibility to +6 more | |
Click to view in NCBI Gene