Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000630671 | SCV000751636 | pathogenic | Duchenne muscular dystrophy | 2017-11-03 | criteria provided, single submitter | clinical testing | This variant is an out-of-frame deletion of the genomic region encompassing exons 12-29 of the DMD gene. This is expected to create a premature translational stop signal and result in an absent or disrupted protein product. Similar deletions of DMD exons 12-29 have been reported in several individuals affected with Duchenne muscular dystrophy (PMID: 19367636, 17253928, 21515508). Loss-of-function variants in DMD are known to be pathogenic (PMID: 16770791, 25007885). For these reasons, this variant has been classified as Pathogenic. |