| | | Single nucleotide variant (nonsense +1 more) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Hepatocellular carcinoma +1 more | |
| | | Deletion (splice donor variant) | Hepatocellular carcinoma | |
| | | Deletion (frameshift variant) | Hepatocellular carcinoma | |
| | | Deletion (splice acceptor variant +1 more) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (intron variant) | Desmoid disease, hereditary +5 more | |
| | | Single nucleotide variant (intron variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | |
| | CTNNB1, LOC126806659 (H517R +1 more) | Single nucleotide variant (missense variant) | Medulloblastoma +7 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hepatocellular carcinoma | |
| | IGF2R, LOC129997612 (R17P) | Single nucleotide variant (missense variant) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Familial adenomatous polyposis 1 +5 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Familial adenomatous polyposis 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | Colorectal cancer +5 more | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +12 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +6 more | |
| | IGF2R, LOC129997612 (R18fs) | Microsatellite (frameshift variant) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Papillary renal cell carcinoma type 1 +5 more | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Duplication (intron variant) | not specified +7 more | |
| | CTNNB1, LOC126806659 (V511fs +1 more) | Duplication (frameshift variant) | Hepatocellular carcinoma | |
| | | Deletion (frameshift variant) | Hepatocellular carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Caudal duplication +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Caudal duplication +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +13 more | |
| | | Single nucleotide variant (missense variant +3 more) | Familial cancer of breast +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Renal cell carcinoma +7 more | |
| | CTNNB1, LOC126806659 (R474* +1 more) | Single nucleotide variant (nonsense) | Microcephalic primordial dwarfism, Alazami type +11 more | |
| | | Single nucleotide variant (nonsense) | not provided +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hepatocellular carcinoma +5 more | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +16 more | |
| | | Single nucleotide variant (missense variant) | Renal cell carcinoma +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Renal cell carcinoma +5 more | |
| | | Single nucleotide variant (missense variant) | Renal cell carcinoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Osteofibrous dysplasia +5 more | GConflicting classifications of pathogenicity |
| | CTNNB1, LOC126806659 (H492fs +1 more) | Duplication (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Renal cell carcinoma +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Osteofibrous dysplasia +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (splice donor variant) | Carcinoma of pancreas +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +8 more | |
| | | Deletion (frameshift variant +2 more) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +6 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | APC-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Desmoid disease, hereditary +5 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Desmoid disease, hereditary +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +4 more) | Desmoid disease, hereditary +5 more | |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +6 more | |
| | | Single nucleotide variant (missense variant) | APC-related condition +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Desmoid disease, hereditary +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Renal cell carcinoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Indel (synonymous variant +1 more) | not specified +6 more | |
| | | Single nucleotide variant (missense variant) | Hepatocellular carcinoma | |
| | | Duplication (frameshift variant) | Familial adenomatous polyposis 1 +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Familial cancer of breast +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Adrenocortical carcinoma, hereditary +12 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial adenomatous polyposis 1 +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 97 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Renal cell carcinoma +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Renal cell carcinoma +6 more | |
| | | Single nucleotide variant (missense variant) | Osteofibrous dysplasia +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +8 more | |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Desmoid disease, hereditary +9 more | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Seborrheic keratosis +14 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Li-Fraumeni syndrome 1 +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |