ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.2303del (p.Cys768fs)

dbSNP: rs2102546166
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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 RCV001384972 SCV001584679 pathogenic not provided 2022-10-05 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with USH2A-related conditions. This sequence change creates a premature translational stop signal (p.Cys768Serfs*20) 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). ClinVar contains an entry for this variant (Variation ID: 1072288). For these reasons, this variant has been classified as Pathogenic.

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