Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000465402 | SCV000561496 | likely benign | Hereditary nonpolyposis colon cancer | 2017-10-17 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000567043 | SCV000662420 | likely benign | Hereditary cancer-predisposing syndrome | 2015-11-27 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign |
Gene |
RCV000604490 | SCV000732144 | likely benign | not specified | 2017-02-09 | 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. |
Color | RCV000567043 | SCV000906643 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-01 | criteria provided, single submitter | clinical testing |