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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: 2-149587666-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=149587666&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 149587666,
      "ref": "G",
      "alt": "C",
      "effect": "splice_region_variant",
      "transcript": "NM_015702.3",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "NM_015702.3",
          "protein_id": "NP_056517.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1392,
          "mane_select": "ENST00000303319.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_015702.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "ENST00000303319.10",
          "protein_id": "ENSP00000301920.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1392,
          "mane_select": "NM_015702.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000303319.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "NM_015702.3",
          "protein_id": "NP_056517.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1392,
          "mane_select": "ENST00000303319.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_015702.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "ENST00000303319.10",
          "protein_id": "ENSP00000301920.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1392,
          "mane_select": "NM_015702.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000303319.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "ENST00000934249.1",
          "protein_id": "ENSP00000604308.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 337,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1014,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1487,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934249.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null,
          "transcript": "ENST00000422782.2",
          "protein_id": "ENSP00000408331.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 330,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 993,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1462,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000422782.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-38C>G",
          "hgvs_p": null,
          "transcript": "ENST00000893992.1",
          "protein_id": "ENSP00000564051.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1410,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893992.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-98C>G",
          "hgvs_p": null,
          "transcript": "ENST00000893995.1",
          "protein_id": "ENSP00000564054.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": null,
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          "cdna_length": 1344,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000893995.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
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          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "MMADHC",
          "gene_hgnc_id": 25221,
          "hgvs_c": "c.-185C>G",
          "hgvs_p": null,
          "transcript": "ENST00000949352.1",
          "protein_id": "ENSP00000619411.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "MMADHC",
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          "hgvs_c": "c.-55C>G",
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          "cds_start": null,
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          "cds_start": null,
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        {
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          "gene_symbol": "MMADHC-DT",
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        {
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          "protein_coding": false,
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          "consequences": [
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          "gene_symbol": "MMADHC-DT",
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          "biotype": "pseudogene",
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        {
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          "protein_coding": false,
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          "consequences": [
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          "exon_count": 4,
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          "gene_symbol": "MMADHC-DT",
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          "hgvs_c": "n.-178G>C",
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          "transcript": "ENST00000790986.1",
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          "cdna_length": 648,
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          "biotype": "pseudogene",
          "feature": "ENST00000790986.1"
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        {
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          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
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          "exon_count": 3,
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          "gene_symbol": "MMADHC-DT",
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          "hgvs_c": "n.-151G>C",
          "hgvs_p": null,
          "transcript": "ENST00000790987.1",
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          "cdna_length": 563,
          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "ENST00000790987.1"
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      ],
      "gene_symbol": "MMADHC",
      "gene_hgnc_id": 25221,
      "dbsnp": "rs988301282",
      "frequency_reference_population": 0.00015111298,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 23,
      "gnomad_exomes_af": 0,
      "gnomad_genomes_af": 0.000151113,
      "gnomad_exomes_ac": 0,
      "gnomad_genomes_ac": 23,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6800000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.9900000095367432,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.68,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.193,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.99,
      "spliceai_max_prediction": "Pathogenic",
      "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": "Likely_benign",
      "acmg_criteria": "PP3_Moderate,BP6_Moderate,BS1",
      "acmg_by_gene": [
        {
          "score": -4,
          "benign_score": 6,
          "pathogenic_score": 2,
          "criteria": [
            "PP3_Moderate",
            "BP6_Moderate",
            "BS1"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_015702.3",
          "gene_symbol": "MMADHC",
          "hgnc_id": 25221,
          "effects": [
            "splice_region_variant"
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          "inheritance_mode": "AR",
          "hgvs_c": "c.-55C>G",
          "hgvs_p": null
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PP3_Moderate",
            "BP6_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000449714.3",
          "gene_symbol": "MMADHC-DT",
          "hgnc_id": 41087,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.361G>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.