| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | PTEN hamartoma tumor syndrome | |
| | | Single nucleotide variant (nonsense +2 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Deletion (frameshift variant +2 more) | Meningioma | |
| | | Deletion (intron variant) | Meningioma | |
Click to view in NCBI Gene