The solution will be used by clinical scientists from the regional healthcare system as well as researchers from the universities. They will log into the NCG HPC system and access the solution preferably through third party interpretation software, or directly via an internet browser. With the genetic variant database software/tool they should be able to filter variants based on several criteria, e.g. mutation type, pathogenicity score, disease, location in gene/genome, etc. This section clarifies that any standard terms that are in conflict with the described use of licenses are set a side.