In order to use UMD Predictor you need to have a validated account or register. UMD-Predictor is freely available for non-commercial users. Nevertheless it is not allowed to copy all or part of the database content without specific authorisation from us. If you are a commercial user. Please contact us to obtain a dedicated license. For more information please contact Prof. As underlined by Pabinger et al.

To submit a nucleotide variant file to the pipeline for processing. Nucleotide variant files in the format described below, typical of Otogenetics exome-sequencing results, which will be processed by the pipeline to provide PROVEAN scores and PubMed cross-references.

Entry points are searches by specific coordinate, dbSNP, or gene; or a comparison of cohorts based on populations in RVS. The first four queries are also wrapped in our REST API. Enter one or more genes and, optionally, genetic variants to search RVS. Enter a phenotype or disease name, and optionally a gene to search. Some pages require an HTML5-capable w.