CancerVar:a web server for improved evidence-based clinical interpretation for cancer somatic mutations

CancerVar is a bioinformatics software tool for clinical interpretation of somatic variants.


Search your exonic variants from pre-built CancerVar databases(updated: with 11 Million mutations in 1685 cancer census gene):
This server is for exon variants, CNVs and some known indels interpretation only, if you have novel indels, you need to download the CancerVar tool from github, then interpret your variant on local.



Please select the  genomic version  and   cancer type



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