| | | Single nucleotide variant (synonymous variant) | not provided +6 more | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Microsatellite (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | Astrocytoma, anaplastic +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (synonymous variant) | Li-Fraumeni syndrome 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Malignant tumor of esophagus | |
| | | Single nucleotide variant (nonsense) | Colorectal cancer +6 more | |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Malignant tumor of esophagus | |
| | | Single nucleotide variant (missense variant) | Choroid plexus papilloma +15 more | |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Colorectal cancer +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome | |
| | | Deletion (inframe_deletion +1 more) | Colorectal cancer | |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Squamous cell carcinoma of the head and neck +3 more | |
| | | Deletion (frameshift variant) | Malignant tumor of esophagus | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |