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Cortexa research tool·genomics·protvar
ProtVar Map Variant
Map a human protein variant to genomic coordinates and get pathogenicity predictions (AlphaMissense, EVE, ESM, conservation). Accepts three input formats: (1) protein 'ACCESSION CHANGE' e.g. 'P04637 R175H'; (2) dbSNP rsID e.g. 'rs1799966'; (3) VCF-style genomic 'chr17 43057065 . T G'. Returns isoform mappings, consequence type, and variant effect scores.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
JSON · 12 lines · 420 chars
Examples (1)
Default ProtVar Map Variant call
public-safeinput
JSON · 3 lines · 19 chars
Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_ProtVar_map_variant
- Tool name
- ProtVar_map_variant
- Added
- 2026-04-30 22:47Z
- Tags
- tooluniverse