SNP Annotation Tool

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Query information, plots and filters

➤ Query ID: nar2020

➤ Human Assembly: GRCh38/hg38

➤ Number of variations: 20525

Export your annotation results as:

✦ These results will be available until 12:10 p.m., 16 Feb 2020 (GMT)

Plots and Graphical representations:

Karyotype of genomic consequences

Predicted functional consequences

Karyotype of predicted deleteriousness

Bar plot of predicted deleterious effect

Reactome Pathways Enrichment Graph

Show filters

Type of Variant:

Minor Allele Global Frequency Threshold:

≤

✷ Show variants with global population freq. lower or equal than the threshold (e.g. 0.1)

Include variants without population data in the results

Gene(s):

Add Genes to filter or leave empty to query all Genes

Genomic Consequence:

Predicted Effect (SIFT/PolyPhen):

Phenotype Association:

Pathway(s):

Add Pathways to filter or leave empty to query all Pathways

Annotation Results

Genomic Coordinates
Overlapped or Nearest Genes

Ensembl
RefSeq

SIFT
PolyPhen

ClinVar
COSMIC

Reactome

Plots and Graphical representations:

Genomic Coordinates and Overlapping

Gene/Protein Consequences

Effect of Non-synonymous Coding SNPs on Protein Function

Population Data

Phenotype & Disease Association

Pathway Analysis