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. Check our video tutorial.

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.

(*) By entering a .com email address, you are giving permission for a QMUL representative to contact you

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