Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000156001 | SCV000205713 | pathogenic | Rare genetic deafness | 2013-08-01 | criteria provided, single submitter | clinical testing | The Deletion of Exons 22-24 in USH2A has not been reported in the literature nor previously identified by our laboratory. This variant is a multi-exonic deletio n encompassing exons 22-24 of USH2A and is predicted to result in an absent or t runcated protein. Several large deletions that span one or more exons of the USH 2A gene have been reported in probands affected with Usher syndrome type II (Ber nal 2005, Baux 2007, Dreyer 2008, Stabej 2012). In summary, this variant meets o ur criteria to be classified as pathogenic (http:/pcpgm.partners.org/LMM). |