| | | Single nucleotide variant (5 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Hereditary nonpolyposis colorectal neoplasms +6 more | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Microsatellite (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Deletion (intron variant) | Lynch syndrome 5 +5 more | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Duplication (intron variant) | not specified +1 more | |
| | | Duplication (intron variant) | Lynch syndrome | |
| | | Deletion (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +3 more | |
| | | Microsatellite (splice donor variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (nonsense) | Lynch syndrome | |