ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.3384-1G>A (rs776963381)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000548461 SCV000629682 likely pathogenic Werner syndrome 2017-04-10 criteria provided, single submitter clinical testing This sequence change affects an acceptor splice site in intron 28 of the WRN gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with a WRN-related disease. In summary, donor and acceptor splice site variants are typically loss-of-function (PMID: 16199547), and loss-of-function variants in WRN are known to be pathogenic (PMID: 16673358). However, without additional functional and/or genetic data, this variant has been classified as Likely Pathogenic.

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