ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.92del (p.Tyr31fs)

dbSNP: rs2144009190
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001982899 SCV002243709 pathogenic Familial meningioma 2024-08-11 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr31Serfs*40) in the SMARCE1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SMARCE1 are known to be pathogenic (PMID: 23377182). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SMARCE1-related conditions. ClinVar contains an entry for this variant (Variation ID: 1459773). For these reasons, this variant has been classified as Pathogenic.
Baylor Genetics RCV001982899 SCV004205058 likely pathogenic Familial meningioma 2023-01-11 criteria provided, single submitter clinical testing

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