| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Copy number loss | Lynch syndrome 1 | |
| | | Deletion (frameshift variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene