Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000801988 | SCV000941794 | pathogenic | Neuronal ceroid lipofuscinosis | 2019-12-10 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the CLN8 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 deletions have been observed in individuals with neuronal ceroid lipofuscinoses (PMID: 28116333). Loss-of-function variants in CLN8 are known to be pathogenic (PMID: 15024724). For these reasons, this variant has been classified as Pathogenic. |