> For the complete documentation index, see [llms.txt](https://vci-gci-docs.clinicalgenome.org/vci-gci-docs/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://vci-gci-docs.clinicalgenome.org/vci-gci-docs/vci-help/starting-an-interpretation/interpretation-mode-view.md).
# Interpretation mode view
SOP Section 5.3
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.
**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.
**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.
The **Evidence Tabs** will now be populated with the [ACMG criteria](https://www.acmg.net/docs/standards_guidelines_for_the_interpretation_of_sequence_variants.pdf) evaluations where you can indicate whether an individual criterion is “Met” (see [Evaluating Criteria](/vci-gci-docs/vci-help/evaluating-criteria.md)).
---
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