| | | Deletion | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (genic upstream transcript variant) | Colorectal cancer, hereditary nonpolyposis, type 2 +6 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Deletion (frameshift variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome +4 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +2 more | |
| | | Single nucleotide variant (nonsense +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Muir-Torré syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant +2 more) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (splice donor variant +1 more) | Lynch syndrome | |
| | | Microsatellite (inframe_deletion +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Breast and/or ovarian cancer +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +3 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome +4 more | |
| | | Deletion (frameshift variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Breast and/or ovarian cancer +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Deletion (frameshift variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Ovarian cancer +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (splice donor variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +3 more | |
| | | Single nucleotide variant (splice acceptor variant) | Lynch syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Colorectal cancer, hereditary nonpolyposis, type 2 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome +4 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (splice donor variant +1 more) | Lynch syndrome | |