OncoGx Biology & Variant Interpreter
Genomic, protein, pathway, and literature context powered by live public APIs
Do not enter patient identifiers, raw genomic files (VCF, FASTQ), family medical records, or any protected health information. Searches go straight from your browser to the public data providers listed below.
Start with one gene or one change
Type a gene, a protein change, an rsID or an HGVS string. The interpreter works out what you typed, asks each public source only what it can answer, and shows where the sources agree or have gaps.
- GeneWhat is this gene, where does it sit, and what does it do?
- VariantWhat does this change do to the transcript and protein?
- ProteinWhich domains, modifications and structures are known?
- PathwayWhich pathways involve it, and what does it interact with?
- LiteratureWhat has been published, and where can I read it?
How your searches are handled
OncoGx has no server behind this page. Each search is sent directly from your browser to the selected public providers, and results live only in this tab's memory.
Refreshing the page or pressing Clear session removes everything. No cookies, browser storage, analytics or search history are used. Each provider may keep its own request logs under its own policy.
What is the OncoGx Biology & Variant Interpreter?
A free research and learning tool that gathers public information about a cancer-related gene, variant, protein or pathway in one place. It queries sources such as Ensembl, MyGene.info, MyVariant.info, UniProt and Europe PMC live from your browser.
Can it tell me what my genetic test result means?
No. It shows what public databases say about a gene or variant in general. What a result means for you depends on your personal and family history and the test itself. A genetic counsellor or your oncology team can explain your report.
Does OncoGx store what I search?
No. Searches go directly from your browser to the public data sources and are not stored by OncoGx. Please do not type names or other details that could identify a person.
Where does the data come from?
From public scientific databases, including Ensembl, MyGene.info, MyVariant.info, UniProt, Europe PMC and other open sources named in the tool. Each result shows its source so you can check the original record.