Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000197573 | SCV000253980 | pathogenic | Bardet-Biedl syndrome | 2015-09-02 | criteria provided, single submitter | clinical testing | This variant is a gross deletion of the genomic region encompassing exons 2-4 of the BBS9 gene. The 3' boundary is likely confined to the intronic region between exons 4 and 5; the 5' end of this event is unknown as it extends to the edge of the assayed region and may encompass additional genes. While this particular variant has not been reported in the literature, exon deletions of BBS9 are known to be pathogenic (PMID: 20177705, 22353939). This deletion is also predicted to eliminate the translation start codon of the BBS9 mRNA and result in an absent or truncated protein. For these reasons, this variant has been classified as Pathogenic. |