Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000638027 | SCV000759507 | pathogenic | Hereditary breast ovarian cancer syndrome | 2017-11-09 | criteria provided, single submitter | clinical testing | This variant is an out-of-frame deletion of the genomic region encompassing exons 4-9 of the BRCA1 gene. This is expected to create a premature translational stop signal and result in an absent or disrupted protein product. This variant has been reported in an individual affected with breast and/or ovarian cancer (PMID: 18783588). This variant is also known as deletion of exons 5-10 in the literature, due to alternative exon nomenclature. ClinVar contains an entry for this variant (Variation ID: 267506) Loss-of-function variants in BRCA1 are known to be pathogenic (PMID: 20104584). For these reasons, this variant has been classified as Pathogenic. |