| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Insertion (5 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Duplication (5 prime UTR variant +2 more) | not specified +2 more | |
| | | Microsatellite (5 prime UTR variant +2 more) | not provided +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene