Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001381808 | SCV001580324 | pathogenic | Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | 2020-10-10 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the CA5A 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 not been reported in the literature in individuals with CA5A-related conditions. Loss-of-function variants in CA5A are known to be pathogenic (PMID: 24530203, 26913920). For these reasons, this variant has been classified as Pathogenic. |