Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001033914 | SCV001197221 | pathogenic | Ornithine carbamoyltransferase deficiency | 2019-08-01 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the OTC 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. This variant has been observed in several individuals affected with OTC deficiency (PMID: 22494545, 11793468, 19475717, 22382802, 18487280, 19138872, 19783189). Loss-of-function variants in OTC are known to be pathogenic (PMID: 10946359, 16786505). For these reasons, this variant has been classified as Pathogenic. |