Releases
v4.31
New documentation links and continuous maintenance
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[4.31]
Added
gnomAD annotation field in admin guide
Export also dynamic panel genes not associated to an HPO term when downloading the HPO panel
Primary HGNC transcript info in variant export files
Show variant quality (QUAL field from vcf) in the variant summary
Load/update PDF gene fusion reports (clinical and research) generated with Arriba
Support new MANE annotations from VEP (both MANE Select and MANE Plus Clinical)
Display on case activity the event of a user resetting all dismissed variants
Support gnomAD population frequencies for mitochondrial variants
Anchor links in Casedata ClinVar panels to redirect after renaming individuals
Fixed
Replace old docs link www.clinicalgenomics.se/scout with new https://clinical-genomics.github.io/scout
Page formatting issues whenever case and variant comments contain extremely long strings with no spaces
Chromograph images can be one column and have scrollbar. Removed legacy code.
Column labels for ClinVar case submission
Page crashing looking for LoqusDB observation when variant doesn't exist
Missing inheritance models and custom inheritance models on newly created gene panels
Accept only numbers in managed variants filter as position and end coordinates
SNP id format and links in Variant page, ClinVar submission form and general report
Case groups tooltip triggered only when mouse is on the panel header
Changed
A more compact case groups panel
Added landscape orientation CSS style to cancer coverage and QC demo report
Improve user documentation to create and save new gene panels
Removed option to use space as separator when uploading gene panels
Separating the columns of standard and custom inheritance models in gene panels
Improved ClinVar instructions for users using non-English Excel
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