# Download variants Exporting annotated variant data facilitates collaboration and record-keeping. To start the download, click the Export icon at the top of the Analysis Tools tab. The XLSX export file contains only the variants visible after applying filters. If your filtered list has more than 1,500 variants, the export file will include only the first 1,500. ## Export file includes the following data: ### Core case and variant identifiers * Case ID * Chromosome * Position * REF * ALT * END * Vartype ### Gene and transcript data * Gene * Transcript * Effect ### Quality metrics * Quality * Depth * Alternate Read * Proband Zygosity * Allele Bias ### Population frequency data * GnomAD AF * GnomAD AC * GnomAD SV AF * GnomAD SV AC * Max AF ### Pathogenicity and interpretation * Pathogenicity * Coding Change * Protein Change * Hom * Hemi * Tag ### Prediction and scoring tools * Prediction * SpliceAI DS AG, AL, DG, DL * SIFT Pred * LRT Pred * MutationTaster Pred * PolyPhen2\_HVAR Pred * PolyPhen2\_HDIV Pred * DANN Score * REVEL Score * CADD Phred Score * PrimateAI3D Score * PrimateAI3D Prediction ### Constraint and gene-level scores * ExAC pLI * gnomAD pLI * Missense z-score * pRec ### Curate and case annotations * Known Variants * Other Family Members * Reference * Evidence Text * Diseases * Disease Inheritance Mode ### Additional case metrics * Phenomeld Score * AI Rank * Individual Genotype * Variant length (kbp) * ISCN * Cytoband * Bin Count * Variant Inheritance --- # Agent Instructions: Querying This Documentation If you need additional information that is not directly available in this page, you can query the documentation dynamically by asking a question. Perform an HTTP GET request on the current page URL with the `ask` query parameter: ``` GET https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/analysis-tools-tab/analysis_tools_tab/variant_table/download_variants.md?ask= ``` The question should be specific, self-contained, and written in natural language. The response will contain a direct answer to the question and relevant excerpts and sources from the documentation. Use this mechanism when the answer is not explicitly present in the current page, you need clarification or additional context, or you want to retrieve related documentation sections.