Modelling functional effects of non-synonymous variants

Submission

VarMod uses structural modelling of proteins, their ligand binding sites and protein-protein interface sites to analyse non-synonymous single nucleotide variants with the aim of identifying those that are likely to be functional and have a role in causing risk or altering disease risk.

Users submit a sequence and a list of variants.  See About for full details on how the method works.
Please use the form below to obtain function predictions for a sequence. See Help for details on the different options available.