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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: 12-111693894-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=111693894&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 12,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "ACAD10",
          "hgnc_id": 21597,
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": -12,
          "transcript": "NM_001136538.2",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_score": -12,
      "allele_count_reference_population": 25430,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.9,
      "chr": "12",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.8999999761581421,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4006,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_025247.6",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000313698.9",
          "protein_coding": true,
          "protein_id": "NP_079523.3",
          "strand": true,
          "transcript": "NM_025247.6",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4006,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000313698.9",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_025247.6",
          "protein_coding": true,
          "protein_id": "ENSP00000325137.5",
          "strand": true,
          "transcript": "ENST00000313698.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1090,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4071,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3273,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000455480.6",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000389813.2",
          "strand": true,
          "transcript": "ENST00000455480.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1342,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 7,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000507135.5",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "n.359+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000507135.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1183,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 5,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000509936.5",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "n.372+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000509936.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1136,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4226,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3411,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 23,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893914.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563973.1",
          "strand": true,
          "transcript": "ENST00000893914.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1134,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4231,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3405,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 23,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893903.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563962.1",
          "strand": true,
          "transcript": "ENST00000893903.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1105,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4140,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3318,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893910.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563969.1",
          "strand": true,
          "transcript": "ENST00000893910.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1090,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4099,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3273,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001136538.2",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001130010.1",
          "strand": true,
          "transcript": "NM_001136538.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1090,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4173,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3273,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893926.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563985.1",
          "strand": true,
          "transcript": "ENST00000893926.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1086,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4089,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3261,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893902.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563961.1",
          "strand": true,
          "transcript": "ENST00000893902.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4014,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893907.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563966.1",
          "strand": true,
          "transcript": "ENST00000893907.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4158,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893912.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 3,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563971.1",
          "strand": true,
          "transcript": "ENST00000893912.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
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          "cdna_length": 4110,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893916.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563975.1",
          "strand": true,
          "transcript": "ENST00000893916.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4095,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000893917.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 3,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000563976.1",
          "strand": true,
          "transcript": "ENST00000893917.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4280,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 23,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000938929.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 4,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000608988.1",
          "strand": true,
          "transcript": "ENST00000938929.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4157,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000948211.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 3,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000618270.1",
          "strand": true,
          "transcript": "ENST00000948211.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4245,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000948213.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000618272.1",
          "strand": true,
          "transcript": "ENST00000948213.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1059,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4110,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3180,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 21,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000948214.1",
          "gene_hgnc_id": 21597,
          "gene_symbol": "ACAD10",
          "hgvs_c": "c.187+998G>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000618273.1",
          "strand": true,
          "transcript": "ENST00000948214.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1058,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
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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.