Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000708317 | SCV000837427 | pathogenic | Carney complex, type 1 | 2018-06-04 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the PRKAR1A 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. A similar whole gene deletion of PRKAR1A has been observed to segregate with disease in a family affected with Carney complex (Invitae). Additionally, whole-gene deletions of PRKAR1A and larger copy number events that include this gene have been reported in individuals affected with Carney complex (PMID: 24170103). Loss-of-function variants in PRKAR1A are known to be pathogenic (PMID: 11115848, 19293268). For these reasons, this variant has been classified as Pathogenic. |