ClinVar Miner

Submissions for variant NM_000535.6(PMS2):c.1145-?_2174+?dup1030

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000240354 SCV000299160 likely pathogenic Lynch syndrome 2016-02-06 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exons 11 and 12 of the PMS2 gene. While the exact position of the duplicated exons cannot be determined from this data, the duplicated copy of this region is likely in tandem and may result in an absent or disrupted protein product. Truncating variants, including gross duplications, in PMS2 are known to be pathogenic (PMID: 21376568, 24362816). A similar duplication of exons 11 and 12 has been reported in the literature in patients subjected to hereditary cancer testing (PMID: 25512458). For these reasons, this variant has been classified as Likely Pathogenic.

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