This test analyzes the MUTYH gene. Individuals who have pathogenic variants in both copies of this gene can develop MUTYH-associated polyposis syndrome (MAP), a colorectal cancer predisposition syndrome. There is evidence to suggest individuals with a pathogenic variant in one copy of MUTYH (heterozygotes) have an increased risk for colorectal cancer.
Genetic testing of this gene may confirm a diagnosis and help guide treatment and management decisions. Identification of a disease-causing variant would also guide testing and diagnosis of at-risk relatives. This test is specifically designed for heritable germline mutations and is not appropriate for the detection of somatic mutations in tumor tissue.
MUTYH can also be ordered as part of a broader panel to test for different types of hereditary cancer, including colorectal cancer. Depending on an individual’s clinical and family history, one of these broader panels may be appropriate. Any of these broader panels can be ordered at no additional charge.
MUTYH-associated polyposis (MAP) is a colorectal cancer predisposition syndrome characterized by the growth of tens to hundreds of adenomatous colorectal polyps. MAP generally has a less severe clinical presentation than familial adenomatous polyposis (FAP), a clinically similar condition in which hundreds to thousands of colorectal polyps develop. Individuals with MAP have a 43%-100% lifetime risk of developing colorectal cancer (PMID: 23035301). Occasionally, affected individuals will develop colorectal cancer in the absence of polyposis. MAP is also associated with an increased risk of developing upper gastrointestinal tract cancers, including duodenal adenomas. Extra-gastrointestinal manifestations have also been reported.
While individuals with a pathogenic variant in one copy of MUTYH (heterozygotes) are not affected with MAP, there is evidence to suggest they have an increased risk of colorectal cancer. Specific cancer risks, however, are not well-established.
Individuals with pathogenic variants in both copies of MUTYH have an increased risk of malignancy compared to the average person, but not everyone with these variants will actually develop cancer. Further, MAP can present differently, even among family members. Because we cannot predict the clinical course, additional medical management strategies focused on cancer prevention and early detection may be beneficial. See the table below for MAP-associated cancer risks:
|MAP-Associated Cancer type||Lifetime risk|
The MUTYH gene is the only gene known to be associated with MAP. Sequence analysis of MUTYH detects approximately 99% of pathogenic variants. The proportion of MAP cases caused by deletions or duplications within the MUTYH gene is unknown but appears to be small.
MAP is inherited in an autosomal recessive pattern. There is some evidence to suggest that individuals who carry a single pathogenic variant may be at increased risk for colorectal cancer.
Approximately 1%-2% of individuals of northern European ancestry are carriers of a MUTYH variant. The prevalence of MAP in this population is estimated at 1 in 20,000 to 1 in 40,000. It is difficult to determine the prevalence of this condition in other ethnicities because the carrier frequency can vary significantly.
Clinical testing for MAP should be considered in individuals with:
Criteria for evaluating a family for MAP have been established by the National Comprehensive Cancer Network:
For management recommendations, please refer to:
Invitae is a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).
Our sequence analysis covers clinically important regions of each gene, including coding exons and 10 to 20 base pairs of adjacent intronic sequence on either side of the coding exons in the transcript listed below. In addition, the analysis covers the select non-coding variants specifically defined in the table below. Any variants that fall outside these regions are not analyzed. Any limitations in the analysis of these genes will be listed on the report. Contact client services with any questions.
Based on validation study results, this assay achieves >99% analytical sensitivity and specificity for single nucleotide variants, insertions and deletions <15bp in length, and exon-level deletions and duplications. Invitae's methods also detect insertions and deletions larger than 15bp but smaller than a full exon but sensitivity for these may be marginally reduced. Invitae’s deletion/duplication analysis determines copy number at a single exon resolution at virtually all targeted exons. However, in rare situations, single-exon copy number events may not be analyzed due to inherent sequence properties or isolated reduction in data quality. Certain types of variants, such as structural rearrangements (e.g. inversions, gene conversion events, translocations, etc.) or variants embedded in sequence with complex architecture (e.g. short tandem repeats or segmental duplications), may not be detected. Additionally, it may not be possible to fully resolve certain details about variants, such as mosaicism, phasing, or mapping ambiguity. Unless explicitly guaranteed, sequence changes in the promoter, non-coding exons, and other non-coding regions are not covered by this assay. Please consult the test definition on our website for details regarding regions or types of variants that are covered or excluded for this test. This report reflects the analysis of an extracted genomic DNA sample. In very rare cases, (circulating hematolymphoid neoplasm, bone marrow transplant, recent blood transfusion) the analyzed DNA may not represent the patient's constitutional genome.
|Gene||Transcript reference||Sequencing analysis||Deletion/Duplication analysis|