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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: 1-180340672-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=180340672&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 180340672,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_032360.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null,
          "transcript": "NM_032360.4",
          "protein_id": "NP_115736.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 282,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 849,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000367595.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_032360.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000367595.4",
          "protein_id": "ENSP00000356567.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 282,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 849,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_032360.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000367595.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.778-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000937021.1",
          "protein_id": "ENSP00000607080.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000937021.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.733-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880422.1",
          "protein_id": "ENSP00000550481.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 305,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 918,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880422.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.676-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000955374.1",
          "protein_id": "ENSP00000625433.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000955374.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000642319.1",
          "protein_id": "ENSP00000495710.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 282,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 849,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000642319.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.574-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880424.1",
          "protein_id": "ENSP00000550483.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 252,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 759,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880424.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.571-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880423.1",
          "protein_id": "ENSP00000550482.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 251,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 756,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880423.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.502-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880421.1",
          "protein_id": "ENSP00000550480.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 228,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 687,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880421.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.313-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000937019.1",
          "protein_id": "ENSP00000607078.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 165,
          "cds_start": null,
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          "cds_length": 498,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": 1,
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          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.223-25950A>G",
          "hgvs_p": null,
          "transcript": "ENST00000937020.1",
          "protein_id": "ENSP00000607079.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 135,
          "cds_start": null,
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          "cds_length": 408,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000937020.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_rank": null,
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          "intron_rank": 6,
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          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null,
          "transcript": "XM_047432080.1",
          "protein_id": "XP_047288036.1",
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          "cds_start": null,
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          "cdna_start": null,
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        {
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          "intron_rank": 6,
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          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
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          "transcript": "XM_047432081.1",
          "protein_id": "XP_047288037.1",
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        },
        {
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          "exon_count": 10,
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          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null,
          "transcript": "XM_047432082.1",
          "protein_id": "XP_047288038.1",
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          "cds_start": null,
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        {
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        {
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          "intron_rank": 6,
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          "gene_symbol": "ACBD6",
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          "hgvs_c": "c.664-25950A>G",
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          "transcript": "XM_047432084.1",
          "protein_id": "XP_047288040.1",
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        {
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          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "c.664-25950A>G",
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          "transcript": "XM_047432085.1",
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        {
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          "biotype": "pseudogene",
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        },
        {
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          "gene_symbol": "ACBD6",
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          "hgvs_c": "n.280-25950A>G",
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          "biotype": "pseudogene",
          "feature": "ENST00000496993.5"
        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ACBD6",
          "gene_hgnc_id": 23339,
          "hgvs_c": "n.664-14110A>G",
          "hgvs_p": null,
          "transcript": "ENST00000645415.1",
          "protein_id": "ENSP00000494507.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000645415.1"
        }
      ],
      "gene_symbol": "ACBD6",
      "gene_hgnc_id": 23339,
      "dbsnp": "rs6670868",
      "frequency_reference_population": 0.050801996,
      "hom_count_reference_population": 250,
      "allele_count_reference_population": 7690,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.050802,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 7690,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 250,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8100000023841858,
      "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": -0.81,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.071,
      "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": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_032360.4",
          "gene_symbol": "ACBD6",
          "hgnc_id": 23339,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.664-25950A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}