ClinVar Miner

Submissions for variant NM_000276.4(OCRL):c.1244+1338_1366del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000795789 SCV000935264 likely pathogenic Lowe syndrome 2018-10-13 criteria provided, single submitter clinical testing This variant is a deletion of the genomic region encompassing exon 13 and part of exon 14 (c.1244+1337_1365del) of the OCRL 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 OCRL-related disease. Loss-of-function variants in OCRL are known to be pathogenic (PMID: 21031565, 22381590). 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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