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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: 19-40692153-A-AT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=40692153&ref=A&alt=AT&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 40692153,
      "ref": "A",
      "alt": "AT",
      "effect": "frameshift_variant",
      "transcript": "NM_024876.4",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "NM_024876.4",
          "protein_id": "NP_079152.3",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000324464.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024876.4"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000324464.8",
          "protein_id": "ENSP00000315118.3",
          "transcript_support_level": 1,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_024876.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000324464.8"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1393dupA",
          "hgvs_p": "p.Ile465fs",
          "transcript": "ENST00000243583.10",
          "protein_id": "ENSP00000243583.5",
          "transcript_support_level": 1,
          "aa_start": 465,
          "aa_end": null,
          "aa_length": 503,
          "cds_start": 1393,
          "cds_end": null,
          "cds_length": 1512,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000243583.10"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1561dupA",
          "hgvs_p": "p.Ile521fs",
          "transcript": "ENST00000871658.1",
          "protein_id": "ENSP00000541717.1",
          "transcript_support_level": null,
          "aa_start": 521,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1561,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871658.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000594720.6",
          "protein_id": "ENSP00000470876.2",
          "transcript_support_level": 5,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000594720.6"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000601967.6",
          "protein_id": "ENSP00000470916.2",
          "transcript_support_level": 3,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000601967.6"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000677018.1",
          "protein_id": "ENSP00000503480.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000677018.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000678404.1",
          "protein_id": "ENSP00000503944.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000678404.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000678419.1",
          "protein_id": "ENSP00000504085.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000678419.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000678467.1",
          "protein_id": "ENSP00000504072.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000678467.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000679130.1",
          "protein_id": "ENSP00000504845.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000679130.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871645.1",
          "protein_id": "ENSP00000541704.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871645.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871646.1",
          "protein_id": "ENSP00000541705.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871646.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871649.1",
          "protein_id": "ENSP00000541708.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871649.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871650.1",
          "protein_id": "ENSP00000541709.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871650.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871651.1",
          "protein_id": "ENSP00000541710.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871651.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871652.1",
          "protein_id": "ENSP00000541711.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871652.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871653.1",
          "protein_id": "ENSP00000541712.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871653.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871655.1",
          "protein_id": "ENSP00000541714.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000871655.1"
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COQ8B",
          "gene_hgnc_id": 19041,
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs",
          "transcript": "ENST00000871661.1",
          "protein_id": "ENSP00000541720.1",
          "transcript_support_level": null,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": 1516,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
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        {
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          "gene_hgnc_id": 19041,
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          "transcript": "ENST00000679315.1",
          "protein_id": "ENSP00000503065.1",
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000679315.1"
        }
      ],
      "gene_symbol": "COQ8B",
      "gene_hgnc_id": 19041,
      "dbsnp": null,
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 1.628,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate,PM2",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PVS1_Moderate",
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_024876.4",
          "gene_symbol": "COQ8B",
          "hgnc_id": 19041,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.1516dupA",
          "hgvs_p": "p.Ile506fs"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}