ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.10626del (p.Glu3542fs)

dbSNP: rs1558095403
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001926140 SCV002188273 pathogenic not provided 2022-09-19 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Glu3542Aspfs*8) in the USH2A gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in USH2A are known to be pathogenic (PMID: 10729113, 10909849, 20507924, 25649381). This variant is present in population databases (no rsID available, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with USH2A-related conditions. ClinVar contains an entry for this variant (Variation ID: 1422442). For these reasons, this variant has been classified as Pathogenic.

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