| | | Duplication (frameshift variant) | Hereditary nonpolyposis colorectal neoplasms +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +3 more | |
| | | Duplication (inframe_insertion) | Hereditary nonpolyposis colorectal neoplasms +4 more | |
| | | Deletion (frameshift variant) | Lynch syndrome 5 +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome +6 more | |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary nonpolyposis colorectal neoplasms +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | |
| | | Single nucleotide variant (missense variant) | Endometrial carcinoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Lynch syndrome 5 +3 more | |
| | | Single nucleotide variant (missense variant) | Mismatch repair cancer syndrome 3 +5 more | |
| | | Deletion (inframe_deletion) | Mismatch repair cancer syndrome 3 +3 more | |
| | | Single nucleotide variant (intron variant) | Endometrial carcinoma +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Endometrial carcinoma +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | |
| | | Single nucleotide variant (missense variant) | Endometrial carcinoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (nonsense) | Hereditary nonpolyposis colorectal neoplasms +4 more | |
| | | Single nucleotide variant (missense variant) | Endometrial carcinoma +3 more | |
| | | Single nucleotide variant (synonymous variant) | MSH6-related condition +5 more | |
| | | Single nucleotide variant (nonsense +1 more) | MSH6-related condition +8 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (splice donor variant) | Hereditary nonpolyposis colorectal neoplasms +8 more | |
| | | Single nucleotide variant (missense variant) | Mismatch repair cancer syndrome 3 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | MSH6-related condition +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Hereditary nonpolyposis colorectal neoplasms +4 more | |
| | | Duplication (frameshift variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +7 more | |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Mismatch repair cancer syndrome 3 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Lynch syndrome | |
| | | Microsatellite (splice donor variant) | Lynch syndrome | |
| | | Duplication (nonsense) | Lynch syndrome | |
| | | Duplication (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Deletion (inframe_indel) | Mismatch repair cancer syndrome 3 | |
| | | Duplication (frameshift variant) | Lynch syndrome | |
| | | Deletion (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Deletion (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Lynch syndrome | |
| | | Duplication (nonsense +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |