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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: 22-33274598-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=33274598&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "22",
      "pos": 33274598,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000397394.8",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_133642.5",
          "protein_id": "NP_598397.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2664,
          "cdna_end": null,
          "cdna_length": 4753,
          "mane_select": "ENST00000397394.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "ENST00000397394.8",
          "protein_id": "ENSP00000380549.2",
          "transcript_support_level": 5,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2664,
          "cdna_end": null,
          "cdna_length": 4753,
          "mane_select": "NM_133642.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "ENST00000354992.7",
          "protein_id": "ENSP00000347088.2",
          "transcript_support_level": 1,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 4193,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.1944C>T",
          "hgvs_p": "p.Asn648Asn",
          "transcript": "ENST00000402320.6",
          "protein_id": "ENSP00000385223.1",
          "transcript_support_level": 1,
          "aa_start": 648,
          "aa_end": null,
          "aa_length": 704,
          "cds_start": 1944,
          "cds_end": null,
          "cds_length": 2115,
          "cdna_start": 2446,
          "cdna_end": null,
          "cdna_length": 3967,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001362949.2",
          "protein_id": "NP_001349878.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2449,
          "cdna_end": null,
          "cdna_length": 4538,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001362951.2",
          "protein_id": "NP_001349880.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2269,
          "cdna_end": null,
          "cdna_length": 4358,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001362953.2",
          "protein_id": "NP_001349882.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2386,
          "cdna_end": null,
          "cdna_length": 4475,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001378624.1",
          "protein_id": "NP_001365553.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2332,
          "cdna_end": null,
          "cdna_length": 4421,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
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          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001378625.1",
          "protein_id": "NP_001365554.1",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2467,
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          "cdna_length": 4556,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
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          "gene_symbol": "LARGE1",
          "gene_hgnc_id": 6511,
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_001378626.1",
          "protein_id": "NP_001365555.1",
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          "cds_start": 2100,
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          "cdna_start": 2404,
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        {
          "aa_ref": "N",
          "aa_alt": "N",
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          "strand": false,
          "consequences": [
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          "gene_symbol": "LARGE1",
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          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn",
          "transcript": "NM_004737.7",
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          "cds_start": 2100,
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          "cdna_start": 2727,
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        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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        {
          "aa_ref": "N",
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        {
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          "gene_symbol": "LARGE1",
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          "hgvs_c": "c.2100C>T",
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        {
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        {
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          "gene_symbol": "LARGE1",
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          "hgvs_c": "c.2100C>T",
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        {
          "aa_ref": "N",
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          "gene_symbol": "LARGE1",
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          "transcript": "ENST00000674668.1",
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        {
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        {
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          "aa_alt": "N",
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        },
        {
          "aa_ref": "N",
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          "consequences": [
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "LARGE1",
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          "hgvs_c": "c.1953C>T",
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          "transcript": "ENST00000674789.1",
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          "biotype": null,
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        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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      ],
      "gene_symbol": "LARGE1",
      "gene_hgnc_id": 6511,
      "dbsnp": "rs17722172",
      "frequency_reference_population": 0.059820414,
      "hom_count_reference_population": 3243,
      "allele_count_reference_population": 96545,
      "gnomad_exomes_af": 0.0612332,
      "gnomad_genomes_af": 0.0462559,
      "gnomad_exomes_ac": 89503,
      "gnomad_genomes_ac": 7042,
      "gnomad_exomes_homalt": 3023,
      "gnomad_genomes_homalt": 220,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6100000143051147,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "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": -0.61,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.165,
      "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": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000397394.8",
          "gene_symbol": "LARGE1",
          "hgnc_id": 6511,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2100C>T",
          "hgvs_p": "p.Asn700Asn"
        }
      ],
      "clinvar_disease": " type A6,Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies),Muscular dystrophy-dystroglycanopathy type B6,not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2 B:6",
      "phenotype_combined": "not specified|Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6|Muscular dystrophy-dystroglycanopathy type B6|not provided",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}