| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (inframe_insertion) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Acute myeloid leukemia | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene