ClinVar Miner

Submissions for variant NC_000005.9:g.(?_112162795)_(112179833_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000808643 SCV000948757 uncertain significance Familial adenomatous polyposis 1 2018-08-15 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exons 12-16 of the APC gene. The 5' boundary is likely confined to intron 11. The 3' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. This particular duplication has not been previously reported in the literature in individuals with an APC-related disease. In summary, the exact genomic location of this variant is unknown and the impact of this duplication on APC protein function has not been established. Therefore, it has been classified as a Variant of Uncertain Significance.

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