ClinVar Miner

Submissions for variant NC_000001.10:g.(?_45793451)_(45798111_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001962996 SCV002232104 pathogenic Familial adenomatous polyposis 2 2021-02-23 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. The region of the MUTYH gene that includes exon(s) 15-16 has been determined to be clinically significant (PMID: 16557584, 17949294, 19806110, 25820570). Therefore, deletions that encompass that region are likely to disrupt protein function and cause disease. This variant has not been reported in the literature in individuals with MUTYH-related conditions. This variant results in the deletion of exon(s) 10-16 and part of exon 9 (c.740_*1527del) of the MUTYH gene. While this deletion is not anticipated to lead to nonsense mediated decay, it is expected to alter mRNA translation or result in a truncated protein product.

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