SNPnexus

barts-and-london_sml

Barts Cancer Institute

SNPnexus is a web-based variant annotation tool designed to simplify and assist in the selection and prioritisation of known and novel genomic alterations.
SNPnexus if freely available for academic and non-profit use only.
If you are a commercial user/service provider, or if you are interested in a customised version of SNPnexus, please contact us on info@snp-nexus.org

Please, enter your institutional email when you run a query - We will notify you when your results are ready.

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Gene/Protein Consequences
Effect of Non-synonymous Coding SNPs on Protein Function
Population Data
1000 Genomes
HapMap
gnomAD Exome Data
gnomAD Genome Data
Regulatory Elements
Conservation
Phenotype & Disease Association
Non-coding Scoring
Structural Variations
Pathway Analysis
Biological / Clinical Interpretation
Gene/Protein Consequences
Effect of Non-synonymous Coding SNPs on Protein Function
Population Data
1000 Genomes
HapMap
gnomAD Exome Data
gnomAD Genome Data
Regulatory Elements
Conservation
Phenotype & Disease Association
Non-coding Scoring
Structural Variations
Pathway Analysis
Biological / Clinical Interpretation