| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 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 +2 more) | Li-Fraumeni syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Li-Fraumeni syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Li-Fraumeni syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Li-Fraumeni syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Squamous cell carcinoma of the head and neck +7 more | |
| | | Single nucleotide variant (missense variant) | PTEN hamartoma tumor syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | PTEN hamartoma tumor syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +7 more | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome 5 +3 more | |
| | | Single nucleotide variant (missense variant) | Breast neoplasm +8 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +5 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +5 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes +1 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +12 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +10 more | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome 5 | |
| | | Single nucleotide variant (missense variant) | Pancreatic adenocarcinoma +21 more | |
| | | Single nucleotide variant (missense variant) | Uterine carcinosarcoma +5 more | |
| | | Single nucleotide variant (missense variant) | CLOVES syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of the large intestine +7 more | |
| | | Single nucleotide variant (missense variant) | Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +15 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +16 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm of uterine cervix +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Neoplasm of uterine cervix +5 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Neoplasm of uterine cervix +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm of uterine cervix +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant neoplasm of body of uterus +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant neoplasm of body of uterus +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant neoplasm of body of uterus +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm of uterine cervix +6 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +6 more | |
| | | Single nucleotide variant (missense variant) | Squamous cell carcinoma of the head and neck +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm of uterine cervix +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Multiple myeloma +5 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +7 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +11 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +11 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +11 more | |
| | | Single nucleotide variant (missense variant) | Uterine carcinosarcoma +11 more | |
| | | Single nucleotide variant (missense variant) | Uterine carcinosarcoma +11 more | |
| | | Single nucleotide variant (missense variant) | Uterine carcinosarcoma +11 more | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +11 more | |
| | | Single nucleotide variant (missense variant) | Breast neoplasm +13 more | |
| | | Single nucleotide variant (missense variant) | Squamous cell carcinoma of the head and neck +13 more | |
| | | Single nucleotide variant (missense variant) | Breast neoplasm +13 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +13 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Breast neoplasm +8 more | |
| | | Single nucleotide variant (missense variant) | Breast neoplasm +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Carcinoma of esophagus +4 more | |
| | | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +5 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +5 more | |
| | | Single nucleotide variant (missense variant) | Adenoid cystic carcinoma +10 more | |
| | | Single nucleotide variant (missense variant) | Rubinstein-Taybi syndrome due to CREBBP mutations | |
| | | Single nucleotide variant (missense variant) | Malignant melanoma of skin +11 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of esophagus +17 more | GPathogenic/Likely pathogenic |
| | CTNNB1, LOC126806658 (S37A +1 more) | Single nucleotide variant (missense variant) | Carcinoma of esophagus +9 more | |
| | CTNNB1, LOC126806658 (S37P +1 more) | Single nucleotide variant (missense variant) | Neoplasm of stomach +9 more | |
| | CTNNB1, LOC126806658 (D32V +1 more) | Single nucleotide variant (missense variant) | Medulloblastoma +8 more | |
| | CTNNB1, LOC126806658 (D32A +1 more) | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +8 more | |
| | CTNNB1, LOC126806658 (D32N +1 more) | Single nucleotide variant (missense variant) | Juvenile nasopharyngeal angiofibroma | |
| | | Single nucleotide variant (missense variant +1 more) | Gastric adenocarcinoma +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes | |
| | CTNNB1, LOC126806658 (D32H +1 more) | Single nucleotide variant (missense variant) | Neoplasm of uterine cervix +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Uterine carcinosarcoma +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Uterine carcinosarcoma +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | Breast neoplasm +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Breast neoplasm +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PTEN hamartoma tumor syndrome | |
| | | Single nucleotide variant (missense variant) | Malignant neoplasm of body of uterus +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PIK3CA related overgrowth syndrome | |
| | | Single nucleotide variant (missense variant) | Small cell lung carcinoma +26 more | GPathogenic/Likely pathogenic; drug response |
| | CTNNB1, LOC126806658 (S37Y +1 more) | Single nucleotide variant (missense variant) | Neoplasm of stomach +10 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Cowden syndrome 5 | |
| | | Single nucleotide variant (missense variant) | Megalencephaly-capillary malformation-polymicrogyria syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm of the large intestine +10 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Large congenital melanocytic nevus +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +3 more | |