| | | Copy number gain | See cases | |
| | LOC130059883, LOC130059884 +922 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | Chromosome 17p13.3 duplication syndrome | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | ALOX12B, ALOX15B +191 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | Vascular endothelial growth factor (VEGF) inhibitor response | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant | not provided | |
| | | Duplication | Li-Fraumeni syndrome 1 +3 more | |
| | | Single nucleotide variant | TP53-related disorder | |
| | | Single nucleotide variant | TP53-related disorder | |
| | | Duplication | Li-Fraumeni syndrome | |
| | | Single nucleotide variant | not provided +1 more | |
| | | Deletion | Li-Fraumeni syndrome | |
| | WRAP53, LOC126862483 +3 more | Deletion | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | TP53-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Deletion (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Deletion (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Deletion (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Li-Fraumeni syndrome 1 | |
| | | Deletion (frameshift variant +3 more) | B-cell chronic lymphocytic leukemia | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Duplication (3 prime UTR variant) | not specified | |
| | LOC126862483, LOC130060171 +3 more | Deletion | Li-Fraumeni syndrome | |
| | LOC130060195, LOC130060196 +141 more | Deletion | Li-Fraumeni syndrome | |
| | | Duplication | Li-Fraumeni syndrome | |
| | | Deletion | Li-Fraumeni syndrome | |
| | | Duplication | Li-Fraumeni syndrome | |
| | | Deletion | Li-Fraumeni syndrome | |
| | KCNAB3, LOC130060206 +141 more | Deletion | Li-Fraumeni syndrome +2 more | |
| | | Deletion | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (stop lost +1 more) | Li-Fraumeni syndrome +1 more | |
| | | Duplication (frameshift variant +2 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (stop lost +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (stop lost +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Duplication (frameshift variant +2 more) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Insertion (frameshift variant +1 more) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Duplication (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Insertion (nonsense +1 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome 1 +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |