feat(ScoreSet): add Clingen allele link to variant details in heatmap and histogram#658
Merged
bencap merged 1 commit intorelease-2026.2.1from May 5, 2026
Merged
Conversation
This file contains hidden or bidirectional Unicode text that may be interpreted or compiled differently than what appears below. To review, open the file in an editor that reveals hidden Unicode characters.
Learn more about bidirectional Unicode characters
Sign up for free
to join this conversation on GitHub.
Already have an account?
Sign in to comment
1 participant
Add this suggestion to a batch that can be applied as a single commit.This suggestion is invalid because no changes were made to the code.Suggestions cannot be applied while the pull request is closed.Suggestions cannot be applied while viewing a subset of changes.Only one suggestion per line can be applied in a batch.Add this suggestion to a batch that can be applied as a single commit.Applying suggestions on deleted lines is not supported.You must change the existing code in this line in order to create a valid suggestion.Outdated suggestions cannot be applied.This suggestion has been applied or marked resolved.Suggestions cannot be applied from pending reviews.Suggestions cannot be applied on multi-line comments.Suggestions cannot be applied while the pull request is queued to merge.Suggestion cannot be applied right now. Please check back later.
This pull request strengthens our linkage of score set and variant pages, adding a link to variant detail pages directly from score set variant tooltips. Previously, users had to search with the HGVS string to reach variant pages.
ClinGen allele support and UI enhancements:
clingenobject with an optionalclingen_allele_idfield to theRawVariantinterface insrc/lib/variants.ts, enabling storage of ClinGen allele IDs.ScoreSetView.vueto include theclingennamespace, ensuring ClinGen data is fetched for each variant.User interface improvements:
ScoreSetHeatmap.vueandScoreSetHistogram.vue, added a "View variant details" link for variants with a ClinGen allele ID, allowing users to quickly access detailed variant pages. [1] [2]