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VEP

Variant Effect Predictor (VEP) determines the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions. Includes EnsEMBL-XS, which provides pre-compiled replacements for frequently used routines in VEP.

homepage: https://www.ensembl.org/info/docs/tools/vep

version toolchain
103.1 GCC/10.2.0
105 GCC/11.2.0
107 GCC/11.3.0
111 GCC/12.2.0
113.0 GCC/12.3.0
113.3 GCC/13.3.0

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