Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001204590 | SCV001375803 | pathogenic | Hereditary breast ovarian cancer syndrome | 2019-09-23 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in BRCA1 are known to be pathogenic (PMID: 20104584). This variant has been observed in an individual affected with breast and/or ovarian cancer (PMID: 29470806). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu1536*) in the BRCA1 gene. It is expected to result in an absent or disrupted protein product. |