This server predicts the functional impact of amino-acid substitutions in proteins, such as mutations discovered in cancer or missense polymorphisms. The functional impact is assessed based on evolutionary conservation of the affected amino acid in protein homologs. The method has been validated on a large set (60k) of disease associated (OMIM) and polymorphic variants. To explore the functional impact of missense mutations found in The Cancer Genome Atlas please use cBioPortal for Cancer Genomics.   Dec 31, 2015    Release   3   is out! All scores for human Swiss-Prot sequences are available:  MA_scores_rel3_swissprot_full.tar.gz  (or split to parts of up to 1M records) (either is 300mb) Also, all human hg19 reference gename nucleic acid variations mappable to Swiss-Prot sequences:  MA_scores_rel3_hg19_full.tar.gz  (or split to parts of up to 1M records) (either is 843mb) Release 2 is available at http://mutationassesor.org/r2/
Enter your mutations read about input format or use example  download as .csv file	Configure output mapping issue      variant based on reference genome start of a codon, isoforms, link to UCSC browser position/residue in Refseq/Uniprot proteins user data (any text after variant printed in separate column) individual scores, misc. msa info number of COSMIC alterations and SNPs in RefSeq protein COSMIC ( detailed) / SNPs in RefSeq position known functional regions of Uniprot protein nearby Pfam domains all Pfam domains in a protein binding sites (directly computed from PDB structures)