Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000797485 | SCV000937044 | pathogenic | Oculofaciocardiodental syndrome | 2018-09-24 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the BCOR gene has been identified. The boundaries of this event are unknown as the deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. Isolated whole-gene deletions of BCOR have not been reported in the literature. However, larger copy number events that include this gene have been reported (PMID: 25620158). Loss-of-function variants in BCOR are known to be pathogenic (PMID: 15004558, 19367324. For these reasons, this variant has been classified as Pathogenic. |