ClinVar Miner

Submissions for variant NM_002354.2(EPCAM):c.(?_-1)_858+?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 RCV000196276 SCV000254698 uncertain significance Lynch syndrome 2015-08-25 criteria provided, single submitter clinical testing This sequence change is a gross duplication of the genomic region encompassing exons 1-7 of the EPCAM gene. This duplication extends to both edges of the assayed region, and the 5' boundary of this event is not known. The 3' boundary is within intron 7, but the exact breakpoint is unknown. This variant has not been published in the literature and is not present in population databases. In summary, this is a novel duplication with uncertain impact on protein function. It has been classified as a Variant of Uncertain Significance.

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