| 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) | Familial cancer of breast +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary breast ovarian cancer syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not specified +10 more | |
| | | Microsatellite (frameshift variant) | Familial cancer of breast +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +4 more | |
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