CancerVar

CancerVar:a web server for improved AI and 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 13 Million mutations in 1911 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:

Query by genomic coordinate

Chr POS: Ref: Alt:

Query by dbSNP ID

rs. :

Query by HGNC gene symbol and cDNA

Gene: cDNA change: c.

Query by HGNC gene symbol and Protein Change

Gene: Protein change: p.

Query by HGNC gene symbol or Alternations

Gene:

CancerVar:

InterVar:

Other tools:

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

Search your exonic variants from pre-built CancerVar databases(updated: with 13 Million mutations in 1911 cancer census gene):