| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Deletion (frameshift variant) | Li-Fraumeni syndrome 2 +19 more | |
| | | Deletion (splice acceptor variant +1 more) | TUMOR PREDISPOSITION SYNDROME 4, BREAST/PROSTATE +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice donor variant) | Hereditary breast ovarian cancer syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Familial cancer of breast +1 more | |
| | | Single nucleotide variant (intron variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (splice donor variant) | Li-Fraumeni syndrome 2 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome 2 +10 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
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