ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.781_784+1375del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001062291 SCV001227080 likely pathogenic not provided 2020-01-06 criteria provided, single submitter clinical testing This variant results in the deletion of part of exon 4 (c.781_784+1375del) of the USH2A gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with USH2A-related conditions. Loss-of-function variants in USH2A are known to be pathogenic (PMID: 10729113, 10909849, 20507924, 25649381). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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