| | | Single nucleotide variant (missense variant) | Neoplasm | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant) | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Duplication (nonsense) | Lynch syndrome 1 | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (nonsense) | Carcinoma of colon | |
| | | Deletion (intron variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | | Indel (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (intron variant) | Carcinoma of colon | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | LOC129933707, LOC129933708 +1 more | Deletion (splice donor variant +1 more) | Carcinoma of colon | |
| | | Microsatellite (frameshift variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Duplication (frameshift variant) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Peutz-Jeghers syndrome | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (synonymous variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice donor variant) | Lynch syndrome 5 | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (splice donor variant +2 more) | Malignant tumor of breast +1 more | |
| | | Deletion (splice acceptor variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Duplication (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant) | Carcinoma of colon | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carcinoma of colon | |
| | | Deletion (nonsense) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (splice donor variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Hereditary breast ovarian cancer syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Deletion (splice acceptor variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 +2 more | |
| | | Deletion (frameshift variant) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Single nucleotide variant (nonsense) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Duplication (frameshift variant) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | not provided +1 more | |
| | | Deletion (splice donor variant +2 more) | Carcinoma of colon +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Duplication (frameshift variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +1 more) | Carcinoma of colon | |
| | | Single nucleotide variant (missense variant +2 more) | Carcinoma of colon | |
| | | Duplication (frameshift variant) | Carcinoma of colon | |
| | | Deletion (splice acceptor variant +2 more) | Carcinoma of colon | |
| | | Deletion (frameshift variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Breast and/or ovarian cancer +2 more | |
| | | Deletion (frameshift variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +2 more | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |