ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.14965A>T (p.Lys4989Ter)

dbSNP: rs770658506
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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 RCV001232854 SCV001405426 pathogenic not provided 2021-08-27 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Lys4989*) 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). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals with USH2A-related conditions. ClinVar contains an entry for this variant (Variation ID: 959490). This variant is not present in population databases (ExAC no frequency).

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