ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.3166C>T (p.Gln1056Ter)

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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 RCV002872027 SCV003234083 pathogenic not provided 2022-09-16 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with USH2A-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gln1056*) 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).
Baylor Genetics RCV003465854 SCV004208275 likely pathogenic Retinitis pigmentosa 39 2023-09-10 criteria provided, single submitter clinical testing

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