WTS outlier genes flagged on SNV-SV-variantS view

[dnil]

Is your feature request related to a problem in the current program to new available techology or software? Please describe and add links/citations if appropriate.
It would be nice if the genes with omics WTS outlier status from DROP, where available, would be flagged on the DNA variantS page.

Describe the solution you'd like
Connecting the right variant might be too difficult at this point, but just highlighting the gene would be nice and seems doable.

Describe alternatives you've considered
One could restrict this to the variant page, or do that as well. From there the RNA alignment button will give some indication.