MutPred2 a predictor of impactful missense variants
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MutDB - A database for assessing the impact of genetic variants. Browse by First Letter of Gene Symbols. An identifier can be gene symbol, protein or transcript RefSeq, dbSNP, SwissVar, or COSMOC identifiers.
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I identified that this domain is operating the Apache/2.4.6 (Red Hat Enterprise Linux) mod_auth_gssapi/1.5.1 mod_auth_kerb/5.4 mod_fcgid/2.3.9 SVN/1.7.14 mod_wsgi/3.4 Python/2.7.5 mod_perl/2.0.9dev Perl/v5.16.3 operating system.PAGE TITLE
MutPred2 a predictor of impactful missense variantsDESCRIPTION
Predict the pathogenicity of amino acid substitutions and their molecular mechanisms. MutPred2 is a standalone and web application developed to classify amino acid substitutions as pathogenic or benign in human. In addition, it predicts their impact on over 50 different protein properties and, thus, enables the inference of molecular mechanisms of pathogenicity. The original MutPred. Web application can still be accessed here. For frameshift and stop-gain variants. We have developed MutPred Splice. Pleas.CONTENT
This website mutpred.mutdb.org had the following on the homepage, "Predict the pathogenicity of amino acid substitutions and their molecular mechanisms." Our analyzers analyzed that the webpage said " MutPred2 is a standalone and web application developed to classify amino acid substitutions as pathogenic or benign in human." The Website also stated " In addition, it predicts their impact on over 50 different protein properties and, thus, enables the inference of molecular mechanisms of pathogenicity. Web application can still be accessed here. For frameshift and stop-gain variants. We have developed MutPred Splice."VIEW OTHER DOMAINS
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