ProtVar

ProtVar helps users to contextualise and evaluate human missense variation at a per-residue level. It can be accessed via genomic coordinates, IDs or protein positions in over 92% of human proteins. Functional and structural annotations, predictions and co-located variants can be explored via an interactive UI or accessed programatically via an API.

Topics

Collections

Details

Maturity:
Mature
Cost:
Free of charge
Tool Type:
api, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Java
Added:
9/21/2023
Last Updated:
9/26/2023

Operations

Data Inputs & Outputs

DNA mapping

Inputs

Outputs

    SNP annotation

    Documentation

    User manual
    https://www.ebi.ac.uk/ProtVar/help
    This is a link to the help section in ProtVar with annotated screen shots to help you navigate the tool and understand the data.

    Links

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