| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not specified +3 more | |
| | | Single nucleotide variant (nonsense +2 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Inversion (missense variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Deletion | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (nonsense +2 more) | Hereditary breast ovarian cancer syndrome +4 more | |
| | | Single nucleotide variant (intron variant +1 more) | Familial cancer of breast +3 more | GPathogenic/Likely pathogenic |
| | | Copy number gain | See cases | |
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