ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.9504C>A (p.Cys3168Ter)

dbSNP: rs2102796365
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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 RCV001970146 SCV002231529 pathogenic not provided 2023-03-27 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Cys3168*) 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 not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with deafness (PMID: 32203226). ClinVar contains an entry for this variant (Variation ID: 1455888). For these reasons, this variant has been classified as Pathogenic.
Baylor Genetics RCV003475228 SCV004200689 pathogenic Retinitis pigmentosa 39 2023-06-06 criteria provided, single submitter clinical testing

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