Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003116587 | SCV003792796 | pathogenic | Genitopatellar syndrome | 2022-08-26 | criteria provided, single submitter | clinical testing | Isolated whole-gene deletions of KAT6B have not been reported in the literature. However, larger copy number events that include this gene have been reported (PMID: 25424711, 27880066). A gross deletion of the genomic region encompassing the full coding sequence of the KAT6B gene has been identified. Loss-of-function variants in KAT6B are known to be pathogenic (PMID: 22077973, 23436491, 25424711). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. For these reasons, this variant has been classified as Pathogenic. |