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Annotate genetic variants and predict functional effects via the Ensembl VEP API.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "VEPmcp" yet — see the docs or source repo.
Use VEPmcp to batch annotate the following human genetic variants and return the gene, transcript consequence, protein impact, and clinical relevance for each: chr7 140453136 A>T; chr17 43045702 C>T; chr13 32316461 G>A.
Structured variant annotation results including gene names, functional consequences, protein changes, and related notes.
Use VEPmcp to analyze the functional impact of variant chr12 25398284 C>A. Explain whether it affects a coding region, the possible amino acid change, and the associated transcript information.
A detailed interpretation of the single variant’s functional impact, including coding effect, amino acid change, and transcript annotation.
Use VEPmcp to process this sample variant list and format the results as a table with columns for variant, gene, consequence type, impact level, and annotation summary, sorted by potential high impact first.
An analysis-ready variant annotation table that helps quickly identify high-impact candidate sites.
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