Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000556502 | SCV000627156 | pathogenic | Osteogenesis imperfecta type I | 2017-08-22 | criteria provided, single submitter | clinical testing | This variant is a gross deletion of the genomic region encompassing all of exons 3-20 and most of exon 2 (c.117_1353+81del) of the COL1A1 gene. This likely creates a premature translational stop signal and is expected to result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with COL1A1-related disease. Loss-of-function variants in COL1A1 are known to be pathogenic (PMID: 7942841, 9295084, 9443882). For these reasons, this variant has been classified as Pathogenic. |