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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 17-775869-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=775869&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 7,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "GLOD4",
          "hgnc_id": 14111,
          "hgvs_c": "c.510G>A",
          "hgvs_p": "p.Glu170Glu",
          "inheritance_mode": "AR",
          "pathogenic_score": 2,
          "score": -5,
          "transcript": "NM_001389725.1",
          "verdict": "Likely_benign"
        }
      ],
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_score": -5,
      "allele_count_reference_population": 1,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.6,
      "chr": "17",
      "clinvar_classification": "Likely benign",
      "clinvar_disease": "not specified",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.6000000238418579,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 298,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1765,
          "cdna_start": 337,
          "cds_end": null,
          "cds_length": 897,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_016080.4",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000301329.11",
          "protein_coding": true,
          "protein_id": "NP_057164.3",
          "strand": false,
          "transcript": "NM_016080.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 298,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1765,
          "cdna_start": 337,
          "cds_end": null,
          "cds_length": 897,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000301329.11",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_016080.4",
          "protein_coding": true,
          "protein_id": "ENSP00000301329.6",
          "strand": false,
          "transcript": "ENST00000301329.11",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 313,
          "aa_ref": "E",
          "aa_start": 119,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1809,
          "cdna_start": 381,
          "cds_end": null,
          "cds_length": 942,
          "cds_start": 357,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000301328.9",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.357G>A",
          "hgvs_p": "p.Glu119Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000301328.5",
          "strand": false,
          "transcript": "ENST00000301328.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 364,
          "aa_ref": "E",
          "aa_start": 170,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1963,
          "cdna_start": 535,
          "cds_end": null,
          "cds_length": 1095,
          "cds_start": 510,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001389725.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.510G>A",
          "hgvs_p": "p.Glu170Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376654.1",
          "strand": false,
          "transcript": "NM_001389725.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 335,
          "aa_ref": "E",
          "aa_start": 141,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1876,
          "cdna_start": 448,
          "cds_end": null,
          "cds_length": 1008,
          "cds_start": 423,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001389726.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.423G>A",
          "hgvs_p": "p.Glu141Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376655.1",
          "strand": false,
          "transcript": "NM_001389726.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 335,
          "aa_ref": "E",
          "aa_start": 141,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1762,
          "cdna_start": 448,
          "cds_end": null,
          "cds_length": 1008,
          "cds_start": 423,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000891260.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.423G>A",
          "hgvs_p": "p.Glu141Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000561319.1",
          "strand": false,
          "transcript": "ENST00000891260.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 326,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1134,
          "cdna_start": 337,
          "cds_end": null,
          "cds_length": 981,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001389727.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376656.1",
          "strand": false,
          "transcript": "NM_001389727.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 313,
          "aa_ref": "E",
          "aa_start": 119,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1810,
          "cdna_start": 382,
          "cds_end": null,
          "cds_length": 942,
          "cds_start": 357,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001366247.2",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.357G>A",
          "hgvs_p": "p.Glu119Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001353176.1",
          "strand": false,
          "transcript": "NM_001366247.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 296,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1830,
          "cdna_start": 398,
          "cds_end": null,
          "cds_length": 891,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000940416.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000610475.1",
          "strand": false,
          "transcript": "ENST00000940416.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 293,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1745,
          "cdna_start": 335,
          "cds_end": null,
          "cds_length": 882,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000940420.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000610479.1",
          "strand": false,
          "transcript": "ENST00000940420.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 293,
          "aa_ref": "E",
          "aa_start": 99,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1760,
          "cdna_start": 340,
          "cds_end": null,
          "cds_length": 882,
          "cds_start": 297,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000956992.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.297G>A",
          "hgvs_p": "p.Glu99Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000627051.1",
          "strand": false,
          "transcript": "ENST00000956992.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 289,
          "aa_ref": "E",
          "aa_start": 95,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2141,
          "cdna_start": 713,
          "cds_end": null,
          "cds_length": 870,
          "cds_start": 285,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001366249.2",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.285G>A",
          "hgvs_p": "p.Glu95Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001353178.1",
          "strand": false,
          "transcript": "NM_001366249.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 289,
          "aa_ref": "E",
          "aa_start": 95,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1838,
          "cdna_start": 410,
          "cds_end": null,
          "cds_length": 870,
          "cds_start": 285,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001366250.2",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.285G>A",
          "hgvs_p": "p.Glu95Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001353179.1",
          "strand": false,
          "transcript": "NM_001366250.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 289,
          "aa_ref": "E",
          "aa_start": 95,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2019,
          "cdna_start": 591,
          "cds_end": null,
          "cds_length": 870,
          "cds_start": 285,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001389728.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.285G>A",
          "hgvs_p": "p.Glu95Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376657.1",
          "strand": false,
          "transcript": "NM_001389728.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 289,
          "aa_ref": "E",
          "aa_start": 95,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1893,
          "cdna_start": 465,
          "cds_end": null,
          "cds_length": 870,
          "cds_start": 285,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001389729.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.285G>A",
          "hgvs_p": "p.Glu95Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376658.1",
          "strand": false,
          "transcript": "NM_001389729.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 289,
          "aa_ref": "E",
          "aa_start": 95,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2040,
          "cdna_start": 612,
          "cds_end": null,
          "cds_length": 870,
          "cds_start": 285,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 10,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001389730.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.285G>A",
          "hgvs_p": "p.Glu95Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376659.1",
          "strand": false,
          "transcript": "NM_001389730.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 285,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1726,
          "cdna_start": 337,
          "cds_end": null,
          "cds_length": 858,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001389731.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376660.1",
          "strand": false,
          "transcript": "NM_001389731.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "E",
          "aa_start": 104,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1711,
          "cdna_start": 337,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 312,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001389732.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.312G>A",
          "hgvs_p": "p.Glu104Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001376661.1",
          "strand": false,
          "transcript": "NM_001389732.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "E",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "E",
          "aa_start": 86,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1770,
          "cdna_start": 332,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 258,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 9,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000940417.1",
          "gene_hgnc_id": 14111,
          "gene_symbol": "GLOD4",
          "hgvs_c": "c.258G>A",
          "hgvs_p": "p.Glu86Glu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000610476.1",
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      ],
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      "effect": "synonymous_variant",
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      "gene_hgnc_id": 14111,
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      "gnomad_exomes_ac": 1,
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      "mitotip_prediction": null,
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      "pathogenicity_classification_combined": "Likely benign",
      "phenotype_combined": "not specified",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": 0.084,
      "pos": 775869,
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      "revel_score": null,
      "splice_prediction_selected": "Benign",
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    }
  ]
}
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