Release version 4.75 (#4296)

* Release version 4.75 * Fix changelog --------- Co-authored-by: Chiara Rasi <[email protected]> Co-authored-by: Daniel Nilsson <[email protected]>
Clinical-Genomics · Dec 20, 2023 · 723f163 · 723f163
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -3,7 +3,8 @@ All notable changes to this project will be documented in this file.
 This project adheres to [Semantic Versioning](http://semver.org/).
 
 About changelog [here](https://keepachangelog.com/en/1.0.0/)
-## [unreleased]
+
+## [4.75]
 ### Added
 - Hovertip to gene panel names with associated genes in variant view, when variant covers more than one gene
 - Tests for panel to genes
@@ -18,7 +19,8 @@ About changelog [here](https://keepachangelog.com/en/1.0.0/)
 - Retrieve and display case and variant custom images using image's saved path
 - Cases are activated by viewing FSHD and SMA reports
 - Split multi-gene SNV variants into single genes when submitting to Matchmaker Exchange
-- Alamut links now appear on the gene level, using transcript and hgvs notation. Less precise, but better for indels.
+- Alamut links also on the gene level, using transcript and HGVS: better for indels. Keep variant link for missing HGVS
+- Thaw WTForms - explicitly coerce form decimal field entries when filters fetched from db
 ### Fixed
 - Removed some extra characters from top of general report left over from FontAwsome fix
 - Do not save fusion variants-specific key/values in other types of variants

diff --git a/scout/__version__.py b/scout/__version__.py
@@ -1 +1 @@
-__version__ = "4.74.1"
+__version__ = "4.75"