Opens a new pop-up window, allows you to manually add a variant.
Opens the CNV analysis modul.
Opens the BamCounter module.
Marks the analysis as not-analysable.
Starts the automatic report generation.
Marks the variant as valid (=true) variant.
Marks the variant as false-positive.
Opens the IGV browser and displays the variant.
Displays additional gene informations.
Displays position of the variant in relation to the protein domains.
Lists all analysed samples harboring the same variant.
Shows additional gene annotations, e.g. dbSNP, COSMIC, ClinVar, SIFT, MutationTaster ...