ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2503del (p.Gln835fs)

dbSNP: rs748484883
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000807064 SCV000947094 pathogenic Werner syndrome 2023-07-07 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 651657). For these reasons, this variant has been classified as Pathogenic. RNA analysis performed to evaluate the impact of this premature translational stop signal on mRNA splicing indicates it does not significantly alter splicing (Invitae). This variant has not been reported in the literature in individuals affected with WRN-related conditions. This variant is present in population databases (rs748484883, gnomAD 0.004%). This sequence change creates a premature translational stop signal (p.Gln835Lysfs*41) in the WRN gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in WRN are known to be pathogenic (PMID: 16673358).
Baylor Genetics RCV000807064 SCV004208847 likely pathogenic Werner syndrome 2023-06-26 criteria provided, single submitter clinical testing

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