Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000218083 | SCV000275142 | likely benign | Hereditary cancer-predisposing syndrome | 2015-04-16 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |
Invitae | RCV000456713 | SCV000561020 | likely benign | Familial cancer of breast | 2024-01-11 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000218083 | SCV000684560 | likely benign | Hereditary cancer-predisposing syndrome | 2016-07-18 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000605748 | SCV000722870 | likely benign | not specified | 2017-09-11 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |