Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NC_000005.10:g.(?_112737024)_(112844136_?)del | APC | Pathogenic | 5 | 112072721 | 112179833 | na | na | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_112707312)_(112780913_?)del | APC | Pathogenic | 5 | 112043009 | 112116610 | na | na | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_112707312)_(112844136_?)del | APC | Pathogenic | 5 | 112043009 | 112179833 | na | na | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_112766316)_(112844136_?)del | APC | Pathogenic | 5 | 112102013 | 112179833 | na | na | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_112827098)_(112844136_?)del | APC | Pathogenic | 5 | 112162795 | 112179833 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000038.6(APC):c.532-2A>C | APC | Pathogenic | 5 | 112116485 | 112116485 | A | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000038.6(APC):c.1627-2A>G | APC | Likely pathogenic | 5 | 112164551 | 112164551 | A | G | criteria provided, single submitter | - |
Indel | NM_000038.6(APC):c.1744-6_1744-4delinsAG | APC | Pathogenic | 5 | 112170642 | 112170644 | TAC | AG | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_80654718)_(80679103_?)del | MSH3 | Pathogenic | 5 | 79950537 | 79974922 | na | na | criteria provided, single submitter | - |
Deletion | NC_000005.10:g.(?_112707312)_(112844126_?)del | APC | Pathogenic | 5 | 112043009 | 112179823 | na | na | criteria provided, single submitter | - |