| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Deletion (nonsense) | Fanconi anemia complementation group J +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Breast carcinoma +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi anemia complementation group J +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | Neoplasm of ovary +7 more | GConflicting classifications of pathogenicity |
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