Upload human SNPs in VCF format

At the moment, MutationExplorer automatically loads AlphaFold models for human transcripts with 2700 or fewer residues. GRCh38 coordinates are required in the VCF file, which is forwarded to ENSEMBL VEP to identify missense variant(s). Only missense variants which impact canonical UniProtKB/Swiss-Prot transcripts are further explored.

Details of the workflow are outlined in FAQs.

Upload a VCF file

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