Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000206725 | SCV000259288 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-04-07 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000421197 | SCV000516864 | likely benign | not specified | 2016-12-12 | 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. |
Ambry Genetics | RCV000563528 | SCV000662488 | likely benign | Hereditary cancer-predisposing syndrome | 2016-06-29 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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. |
Color Diagnostics, |
RCV000563528 | SCV000908417 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-09 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV003997559 | SCV004835049 | likely benign | Lynch syndrome | 2023-06-08 | criteria provided, single submitter | clinical testing |