Interpretation mode view
SOP Section 5.3
PreviousStarting an InterpretationNextAssociating a variant with disease, mode of inheritance and specification document
Last updated
SOP Section 5.3
Last updated
Once in Interpretation mode, the following options will appear:
A. Click to view a summary of all criteria evaluations.
B. Click to view the complete history of curation actions for this interpretation record. Note: It will not include actions from other interpretations of this variant.
F. The Progress bar indicates the strength of criteria met and the auto-calculated pathogenicity.
G. The Criteria bar displays all ACMG criteria codes. Scroll over a code to display its description. Click on a code to navigate to the pertinent section in the VCI.
C. Click to add a specification document to the curation
D. Click or "Add Disease +" under "My Interpretation" to associate a disease with the variant.
E. Click to add mode of inheritance.
The Evidence Tabs will now be populated with the evaluations where you can indicate whether an individual criterion is “Met” (see Evaluating Criteria).
