Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000817284 | SCV000957834 | pathogenic | Hyper-IgM syndrome type 1 | 2019-06-21 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the CD40LG 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. Similar gross deletions of CD40LG have been reported in individuals affected with hyper IgM syndrome (PMID: PMID: 15358621, 16019685). Loss-of-function variants in CD40LG are known to be pathogenic (PMID: 15319456). For these reasons, this variant has been classified as Pathogenic. |