VEP stands for Variant Effect Predictor. It is a tool developed by Ensembl that predicts the functional effects of genomic variants (SNPs, insertions, deletions, etc.) on genes, transcripts, and protein products. VEP annotates variants with information such as the genes they overlap, the consequence type of the variant (e.g., missense, frameshift), and any known clinical associations. It is commonly used in genomic research and clinical settings to interpret the potential impact of genetic variations.
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