SNPnexus

barts-and-london_sml

Barts Cancer Institute

Add your email here if you want to be notified when your query is ready (Optional)

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 does not require any installation or registration and is free to use for everyone.

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