Loading of RNA fusion variants, missing icons fix & other

[4.74]

Added

• SNVs and Indels, MEI and str variants genes have links to Decipher
• An owner + case display name index for cases database collection
• Test and fixtures for RNA fusion case page
• Load and display fusion variants from VCF files as the other variant types
• Option to update case document with path to mei variants (clinical and research)

Changed

• Details on variant type and category for audit filters on case general report
• Enable Gens CN profile button also in somatic case view
• Fix case of analysis type check for Gens analysis button - only show for WGS

Fixed

• loqusdb table no longer has empty row below each loqusid
• MatchMaker submission details page crashing because of change in date format returned by PatientMatcher
• Variant external links buttons style does not change color when visited
• Hide compounds with compounds follow filter for region or function would fail for variants in multiple genes
• Updated FontAwesome version to fix missing icons