SIFT drug

External links

DrugBank · PubChem

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Mentioned in (16)

Papers in which this entity is mentioned.

• dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs. (2020)
• Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
• GAVIN: Gene-Aware Variant INterpretation for medical sequencing. (2017)
• Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines. (2017)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel). (2016)
• REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. (2016)
• The human gene damage index as a gene-level approach to prioritizing exome variants. (2015)
• MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
• Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models. (2013)
• Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
• Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)
• SNPs3D: candidate gene and SNP selection for association studies. (2006)
• SIFT: Predicting amino acid changes that affect protein function. (2003)

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