| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Breast carcinoma +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Malignant tumor of breast +11 more | |
| | | Microsatellite (frameshift variant) | Breast-ovarian cancer, familial, susceptibility to, 5 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
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