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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: 12-64497257-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=64497257&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 64497257,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant,splice_region_variant",
      "transcript": "ENST00000331710.10",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "NM_013254.4",
          "protein_id": "NP_037386.1",
          "transcript_support_level": null,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2056,
          "cdna_end": null,
          "cdna_length": 3022,
          "mane_select": "ENST00000331710.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "ENST00000331710.10",
          "protein_id": "ENSP00000329967.5",
          "transcript_support_level": 1,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2056,
          "cdna_end": null,
          "cdna_length": 3022,
          "mane_select": "NM_013254.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "ENST00000650790.1",
          "protein_id": "ENSP00000498995.1",
          "transcript_support_level": null,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2099,
          "cdna_end": null,
          "cdna_length": 3006,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1954G>C",
          "hgvs_p": "p.Glu652Gln",
          "transcript": "ENST00000677641.1",
          "protein_id": "ENSP00000504637.1",
          "transcript_support_level": null,
          "aa_start": 652,
          "aa_end": null,
          "aa_length": 728,
          "cds_start": 1954,
          "cds_end": null,
          "cds_length": 2187,
          "cdna_start": 2083,
          "cdna_end": null,
          "cdna_length": 3001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1942G>C",
          "hgvs_p": "p.Glu648Gln",
          "transcript": "ENST00000677632.1",
          "protein_id": "ENSP00000504586.1",
          "transcript_support_level": null,
          "aa_start": 648,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1942,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": 2041,
          "cdna_end": null,
          "cdna_length": 2959,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "ENST00000652657.1",
          "protein_id": "ENSP00000498887.1",
          "transcript_support_level": null,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": 2064,
          "cdna_end": null,
          "cdna_length": 2944,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1855G>C",
          "hgvs_p": "p.Glu619Gln",
          "transcript": "ENST00000678180.1",
          "protein_id": "ENSP00000504132.1",
          "transcript_support_level": null,
          "aa_start": 619,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 1855,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 1951,
          "cdna_end": null,
          "cdna_length": 2869,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1801G>C",
          "hgvs_p": "p.Glu601Gln",
          "transcript": "ENST00000651014.1",
          "protein_id": "ENSP00000498885.1",
          "transcript_support_level": null,
          "aa_start": 601,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1801,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 2145,
          "cdna_end": null,
          "cdna_length": 3046,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1801G>C",
          "hgvs_p": "p.Glu601Gln",
          "transcript": "ENST00000676912.1",
          "protein_id": "ENSP00000503567.1",
          "transcript_support_level": null,
          "aa_start": 601,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1801,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 2004,
          "cdna_end": null,
          "cdna_length": 2956,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1699G>C",
          "hgvs_p": "p.Glu567Gln",
          "transcript": "ENST00000650762.1",
          "protein_id": "ENSP00000498758.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 643,
          "cds_start": 1699,
          "cds_end": null,
          "cds_length": 1932,
          "cdna_start": 1866,
          "cdna_end": null,
          "cdna_length": 2459,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1609G>C",
          "hgvs_p": "p.Glu537Gln",
          "transcript": "ENST00000676930.1",
          "protein_id": "ENSP00000502899.1",
          "transcript_support_level": null,
          "aa_start": 537,
          "aa_end": null,
          "aa_length": 613,
          "cds_start": 1609,
          "cds_end": null,
          "cds_length": 1842,
          "cdna_start": 1697,
          "cdna_end": null,
          "cdna_length": 2649,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "XM_005268809.2",
          "protein_id": "XP_005268866.1",
          "transcript_support_level": null,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2264,
          "cdna_end": null,
          "cdna_length": 3230,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln",
          "transcript": "XM_005268810.2",
          "protein_id": "XP_005268867.1",
          "transcript_support_level": null,
          "aa_start": 653,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1957,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2507,
          "cdna_end": null,
          "cdna_length": 3473,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.863G>C",
          "hgvs_p": null,
          "transcript": "ENST00000545392.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1781,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*366G>C",
          "hgvs_p": null,
          "transcript": "ENST00000650708.1",
          "protein_id": "ENSP00000498667.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2751,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*2102G>C",
          "hgvs_p": null,
          "transcript": "ENST00000650786.1",
          "protein_id": "ENSP00000498280.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3244,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.1957G>C",
          "hgvs_p": null,
          "transcript": "ENST00000650997.1",
          "protein_id": "ENSP00000498341.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 3178,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*224G>C",
          "hgvs_p": null,
          "transcript": "ENST00000651262.1",
          "protein_id": "ENSP00000498461.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2902,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*1441G>C",
          "hgvs_p": null,
          "transcript": "ENST00000651878.1",
          "protein_id": "ENSP00000499077.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3151,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*337G>C",
          "hgvs_p": null,
          "transcript": "ENST00000652537.1",
          "protein_id": "ENSP00000499102.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
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      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.058166325092315674,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.03799999877810478,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": 0.067,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0889,
      "alphamissense_prediction": "Benign",
      "bayesdelnoaf_score": -0.63,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 4.129,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.0012422250309014,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Strong,BP6",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 5,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000331710.10",
          "gene_symbol": "TBK1",
          "hgnc_id": 11584,
          "effects": [
            "missense_variant",
            "splice_region_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.1957G>C",
          "hgvs_p": "p.Glu653Gln"
        }
      ],
      "clinvar_disease": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 4,TBK1-related disorder,not provided",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:2 LB:1",
      "phenotype_combined": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 4|TBK1-related disorder|not provided",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}