get_variant_consequences
Analyze variant impacts on genes and transcripts using variant IDs or HGVS notation. Supports species-specific genomic data and annotations via the Ensembl MCP Server.
Instructions
Predict consequences of variants on genes and transcripts
Input Schema
Name | Required | Description | Default |
---|---|---|---|
species | No | Species name (default: homo_sapiens) | |
variants | Yes | Variant IDs or HGVS notation |