| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +3 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Deletion | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Single nucleotide variant (missense variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (intron variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (intron variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Deletion (splice donor variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Indel (frameshift variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Duplication | Hereditary cancer-predisposing syndrome | |
| | | Duplication | Hereditary cancer-predisposing syndrome | |
| | | Duplication | Hereditary cancer-predisposing syndrome | |
| | | Deletion | not provided | |
| | | Deletion | not provided | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Deletion | Lynch syndrome 1 | |
| | | Deletion | Lynch syndrome 1 | |
| | | Deletion | Lynch syndrome 1 | |
| | | Insertion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Colon cancer | |
| | | Insertion | Lynch syndrome 1 | |
| | | Deletion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Indel (splice acceptor variant +2 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Indel (splice acceptor variant +1 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Duplication | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome 1 | |
| | | Deletion | not provided | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (splice donor variant +1 more) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Lynch syndrome | |
| | | Insertion (splice donor variant) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Duplication | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion (inframe_deletion +4 more) | Lynch syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion (splice acceptor variant +1 more) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |
| | | Deletion | Lynch syndrome | |