Allow GCI users to see useful VCI information about variants.
1) When users add in a Variant ID, see if there is a VCI interpretation for the variant. For display of variant, the suggestion is to use the “All interpretations table" as a template: Variant title, Variant ID(s), Disease name/MONDO, MOI, Creator, Date created
& if an interpretation has a status of Approved in the VCI then there would be the chainlink present to link to the viewable evidence summary
2) HMAF in Evidence Summary Table (see #1606)
3) It would be nice to be able to initiate a VCI interpretation from within the GCI when adding variants.
4) It would be nice to be able to see the predictor information in the GCI.
wrightmw
commented
2 years ago
Allow GCI users to see useful VCI information about variants.
1) When users add in a Variant ID, see if there is a VCI interpretation for the variant. For display of variant, the suggestion is to use the “All interpretations table" as a template: Variant title, Variant ID(s), Disease name/MONDO, MOI, Creator, Date created & if an interpretation has a status of Approved in the VCI then there would be the chainlink present to link to the viewable evidence summary
2) HMAF in Evidence Summary Table (see #1606)
3) It would be nice to be able to initiate a VCI interpretation from within the GCI when adding variants.
4) It would be nice to be able to see the predictor information in the GCI.