Upload a VCF file
Upload a Variant Call Format (VCF) file from your sequencing pipeline. MutVar maps genomic coordinates to protein variants via Ensembl VEP and retrieves precomputed pathogenicity predictions for all missense variants found in our dataset.
1Parse VCF
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2Map to protein (Ensembl VEP)
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3Lookup MutVar predictions
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4Results + export
Drop your VCF file here
or click to browse — .vcf and .vcf.gz supported
or paste VCF content directly
Don't have a VCF file?
Your VCF file is processed entirely in your browser. Variant coordinates are sent only to the public Ensembl VEP REST API (EMBL-EBI) for genomic annotation. No data is stored on our servers.