| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Indel (intron variant) | not provided | |
| | | Indel (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
| | | Indel (frameshift variant +3 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 4 | |
| | | Deletion (frameshift variant +3 more) | Lynch syndrome 4 | |
| | | Deletion (frameshift variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +3 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (intron variant +3 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +3 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 4 | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 4 | |
| | | Deletion (frameshift variant +1 more) | Lynch syndrome 4 | |
| | | Deletion (frameshift variant +3 more) | Lynch syndrome 4 | |
| | | Duplication | Lynch syndrome 4 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion | not provided | |
| | | Deletion (splice acceptor variant) | Lynch syndrome 4 | |
| | | Deletion | Lynch syndrome 4 | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not provided | |
| | | Copy number gain | Lynch syndrome 4 +1 more | |
| | | Deletion (frameshift variant +2 more) | Lynch syndrome 4 | |
| | | Deletion | Hereditary nonpolyposis colon cancer | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary cancer-predisposing syndrome | |
| | | Deletion | Mismatch repair cancer syndrome 1 | |
| | | Insertion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary cancer-predisposing syndrome | |
| | | Duplication | not provided | |
| | | Deletion | not provided | |
| | | Duplication | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Duplication | Lynch syndrome 1 | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Insertion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |