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Variant Annotation
Provide a VCF by pasting contents, uploading a file, or selecting an existing OmniObject. Then choose organism and genome build.
Ready
Inputs v1
Inputs
Choose one input type
Input type
Paste VCF
Upload VCF
OmniObject VCF
Backend should honor
input_source
. For large files, prefer Upload or OmniObject.
Paste VCF (text)
Paste a small VCF for testing. For real runs, use Upload or OmniObject.
Upload VCF
Upload a .vcf or .vcf.gz file.
Select OmniObject
(0 available)
-- Select --
No objects returned. Ensure you're reading
work/object_registry.json
.
Tool & Options
Organism → Build
Annotation tool
SnpEff
ANNOVAR
VEP
bcftools csq
Pick one tool for this run.
Organism
-- Select --
Human
Mouse
Rat
Zebrafish
Genome builds will update after selecting organism.
Genome build
-- Select organism first --
Posted as
genome_build
.
Create log
Create run object
Run annotation
Organism/build dependency + downloads shown only after success.
Multi-Source Variant Annotation
Local · No API
Chromosome
Position
Ref
Alt
Assembly
GRCh38
GRCh37
🔍 Annotate from All Sources
🧬 gnomAD v4.0
🏥 ClinVar GRCh38
☢️ COSMIC v104