[x] Rename ClinvarID -> Clinvar. Use clinvar description instead of ID. (Maybe we can make the id available for download)
[x] show both pathogenic germline and somatic by default. Show germline mutations in table on top (sort by germline) Moved to #66
[x] on explore page make it more clear in tooltip what variants you're navigating to. Maybe list number behind it. Could also add links for pathogenic germline and bialellic.
[ ] Update %Biallelic header tooltip description to Percent of germline carriers biallelic in the corresponding tumor sample (if we decide to show total biallelic ratio for Benign/VUS)
[ ] in gene page, style HGVSg (e.g. underlining) to make it more obvious that it’s a hyperlink.
[ ] Hiding additional columns (Age at dx etc...) until we get new data for pathogenic variants
Data
Visual
show both pathogenic germline and somatic by default. Show germline mutations in table on top (sort by germline)Moved to #66Percent of germline carriers biallelic in the corresponding tumor sample(if we decide to show total biallelic ratio for Benign/VUS)URL
Analytics