{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,28]],"date-time":"2026-03-28T15:47:20Z","timestamp":1774712840370,"version":"3.50.1"},"reference-count":5,"publisher":"Oxford University Press (OUP)","issue":"16","license":[{"start":{"date-parts":[[2016,10,2]],"date-time":"2016-10-02T00:00:00Z","timestamp":1475366400000},"content-version":"vor","delay-in-days":2298,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/2.5"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010,8,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Summary: A tool to predict the effect that newly discovered genomic variants have on known transcripts is indispensible in prioritizing and categorizing such variants. In Ensembl, a web-based tool (the SNP Effect Predictor) and API interface can now functionally annotate variants in all Ensembl and Ensembl Genomes supported species.<\/jats:p>\n               <jats:p>Availability: The Ensembl SNP Effect Predictor can be accessed via the Ensembl website at http:\/\/www.ensembl.org\/. The Ensembl API (http:\/\/www.ensembl.org\/info\/docs\/api\/api_installation.html for installation instructions) is open source software.<\/jats:p>\n               <jats:p>Contact: \u00a0wm2@ebi.ac.uk; fiona@ebi.ac.uk<\/jats:p>\n               <jats:p>Supplementary information: \u00a0Supplementary data are available at Bioinformatics online.<\/jats:p>","DOI":"10.1093\/bioinformatics\/btq330","type":"journal-article","created":{"date-parts":[[2010,6,20]],"date-time":"2010-06-20T23:54:25Z","timestamp":1277078065000},"page":"2069-2070","source":"Crossref","is-referenced-by-count":1414,"title":["Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor"],"prefix":"10.1093","volume":"26","author":[{"given":"William","family":"McLaren","sequence":"first","affiliation":[{"name":"1 European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD and 2Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK"}]},{"given":"Bethan","family":"Pritchard","sequence":"additional","affiliation":[{"name":"1 European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD and 2Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK"}]},{"given":"Daniel","family":"Rios","sequence":"additional","affiliation":[{"name":"1 European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD and 2Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK"}]},{"given":"Yuan","family":"Chen","sequence":"additional","affiliation":[{"name":"1 European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD and 2Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK"}]},{"given":"Paul","family":"Flicek","sequence":"additional","affiliation":[{"name":"1 European Bioinformatics Institute, Wellcome 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