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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: 11-112061088-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=112061088&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 112061088,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000280346.11",
      "consequences": [
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1728C>A",
          "hgvs_p": "p.Phe576Leu",
          "transcript": "NM_001931.5",
          "protein_id": "NP_001922.2",
          "transcript_support_level": null,
          "aa_start": 576,
          "aa_end": null,
          "aa_length": 647,
          "cds_start": 1728,
          "cds_end": null,
          "cds_length": 1944,
          "cdna_start": 1793,
          "cdna_end": null,
          "cdna_length": 3878,
          "mane_select": "ENST00000280346.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1728C>A",
          "hgvs_p": "p.Phe576Leu",
          "transcript": "ENST00000280346.11",
          "protein_id": "ENSP00000280346.7",
          "transcript_support_level": 1,
          "aa_start": 576,
          "aa_end": null,
          "aa_length": 647,
          "cds_start": 1728,
          "cds_end": null,
          "cds_length": 1944,
          "cdna_start": 1793,
          "cdna_end": null,
          "cdna_length": 3878,
          "mane_select": "NM_001931.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1746C>A",
          "hgvs_p": "p.Phe582Leu",
          "transcript": "NM_001372031.1",
          "protein_id": "NP_001358960.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 653,
          "cds_start": 1746,
          "cds_end": null,
          "cds_length": 1962,
          "cdna_start": 1811,
          "cdna_end": null,
          "cdna_length": 3896,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1728C>A",
          "hgvs_p": "p.Phe576Leu",
          "transcript": "ENST00000713569.1",
          "protein_id": "ENSP00000518862.1",
          "transcript_support_level": null,
          "aa_start": 576,
          "aa_end": null,
          "aa_length": 647,
          "cds_start": 1728,
          "cds_end": null,
          "cds_length": 1944,
          "cdna_start": 2168,
          "cdna_end": null,
          "cdna_length": 3465,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1722C>A",
          "hgvs_p": "p.Phe574Leu",
          "transcript": "NM_001372032.1",
          "protein_id": "NP_001358961.1",
          "transcript_support_level": null,
          "aa_start": 574,
          "aa_end": null,
          "aa_length": 645,
          "cds_start": 1722,
          "cds_end": null,
          "cds_length": 1938,
          "cdna_start": 1787,
          "cdna_end": null,
          "cdna_length": 3872,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1722C>A",
          "hgvs_p": "p.Phe574Leu",
          "transcript": "ENST00000681316.1",
          "protein_id": "ENSP00000506560.1",
          "transcript_support_level": null,
          "aa_start": 574,
          "aa_end": null,
          "aa_length": 645,
          "cds_start": 1722,
          "cds_end": null,
          "cds_length": 1938,
          "cdna_start": 1769,
          "cdna_end": null,
          "cdna_length": 3825,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1707C>A",
          "hgvs_p": "p.Phe569Leu",
          "transcript": "NM_001372033.1",
          "protein_id": "NP_001358962.1",
          "transcript_support_level": null,
          "aa_start": 569,
          "aa_end": null,
          "aa_length": 640,
          "cds_start": 1707,
          "cds_end": null,
          "cds_length": 1923,
          "cdna_start": 1772,
          "cdna_end": null,
          "cdna_length": 3857,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1707C>A",
          "hgvs_p": "p.Phe569Leu",
          "transcript": "ENST00000681328.1",
          "protein_id": "ENSP00000506355.1",
          "transcript_support_level": null,
          "aa_start": 569,
          "aa_end": null,
          "aa_length": 640,
          "cds_start": 1707,
          "cds_end": null,
          "cds_length": 1923,
          "cdna_start": 1754,
          "cdna_end": null,
          "cdna_length": 3810,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1695C>A",
          "hgvs_p": "p.Phe565Leu",
          "transcript": "NM_001372034.1",
          "protein_id": "NP_001358963.1",
          "transcript_support_level": null,
          "aa_start": 565,
          "aa_end": null,
          "aa_length": 636,
          "cds_start": 1695,
          "cds_end": null,
          "cds_length": 1911,
          "cdna_start": 1760,
          "cdna_end": null,
          "cdna_length": 3845,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1695C>A",
          "hgvs_p": "p.Phe565Leu",
          "transcript": "ENST00000679878.1",
          "protein_id": "ENSP00000505567.1",
          "transcript_support_level": null,
          "aa_start": 565,
          "aa_end": null,
          "aa_length": 636,
          "cds_start": 1695,
          "cds_end": null,
          "cds_length": 1911,
          "cdna_start": 1760,
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          "mane_select": null,
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        {
          "aa_ref": "F",
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          "protein_coding": true,
          "strand": true,
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            "missense_variant"
          ],
          "exon_rank": 12,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1620C>A",
          "hgvs_p": "p.Phe540Leu",
          "transcript": "NM_001372035.1",
          "protein_id": "NP_001358964.1",
          "transcript_support_level": null,
          "aa_start": 540,
          "aa_end": null,
          "aa_length": 611,
          "cds_start": 1620,
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          "cds_length": 1836,
          "cdna_start": 1685,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "F",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "DLAT",
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          "hgvs_c": "c.1620C>A",
          "hgvs_p": "p.Phe540Leu",
          "transcript": "ENST00000681339.1",
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          "cds_start": 1620,
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          "cdna_start": 1667,
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        {
          "aa_ref": "F",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          ],
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          "intron_rank": null,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1602C>A",
          "hgvs_p": "p.Phe534Leu",
          "transcript": "NM_001372036.1",
          "protein_id": "NP_001358965.1",
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          "cds_start": 1602,
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        },
        {
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          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1560C>A",
          "hgvs_p": "p.Phe520Leu",
          "transcript": "NM_001372037.1",
          "protein_id": "NP_001358966.1",
          "transcript_support_level": null,
          "aa_start": 520,
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          "cds_start": 1560,
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          "cdna_start": 1666,
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        },
        {
          "aa_ref": "F",
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          "strand": true,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1473C>A",
          "hgvs_p": "p.Phe491Leu",
          "transcript": "ENST00000680411.1",
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        },
        {
          "aa_ref": "F",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
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          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1449C>A",
          "hgvs_p": "p.Phe483Leu",
          "transcript": "NM_001372038.1",
          "protein_id": "NP_001358967.1",
          "transcript_support_level": null,
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          "feature": null
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        {
          "aa_ref": "F",
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          "canonical": false,
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          "strand": true,
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          "exon_rank": 11,
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1449C>A",
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          "transcript": "ENST00000680331.1",
          "protein_id": "ENSP00000506707.1",
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          "cds_start": 1449,
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        },
        {
          "aa_ref": "F",
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          "intron_rank": null,
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          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1413C>A",
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          "transcript": "NM_001372039.1",
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        },
        {
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          "intron_rank": null,
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          "gene_symbol": "DLAT",
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          "hgvs_c": "c.1413C>A",
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        },
        {
          "aa_ref": "F",
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          ],
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DLAT",
          "gene_hgnc_id": 2896,
          "hgvs_c": "c.1347C>A",
          "hgvs_p": "p.Phe449Leu",
          "transcript": "NM_001372040.1",
          "protein_id": "NP_001358969.1",
          "transcript_support_level": null,
          "aa_start": 449,
          "aa_end": null,
          "aa_length": 520,
          "cds_start": 1347,
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          "cds_length": 1563,
          "cdna_start": 1412,
          "cdna_end": null,
          "cdna_length": 3497,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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      "frequency_reference_population": 0.0000041062926,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 6,
      "gnomad_exomes_af": 0.00000410629,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 6,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.9692670702934265,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.589,
      "revel_prediction": "Uncertain_significance",
      "alphamissense_score": 0.9989,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.15,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 1.94,
      "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": 7,
      "acmg_classification": "Likely_pathogenic",
      "acmg_criteria": "PM2,PP3_Strong,PP5",
      "acmg_by_gene": [
        {
          "score": 7,
          "benign_score": 0,
          "pathogenic_score": 7,
          "criteria": [
            "PM2",
            "PP3_Strong",
            "PP5"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000280346.11",
          "gene_symbol": "DLAT",
          "hgnc_id": 2896,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1728C>A",
          "hgvs_p": "p.Phe576Leu"
        },
        {
          "score": 7,
          "benign_score": 0,
          "pathogenic_score": 7,
          "criteria": [
            "PM2",
            "PP3_Strong",
            "PP5"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "NM_001439210.1",
          "gene_symbol": "PIH1D2",
          "hgnc_id": 25210,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.814-8401G>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Pyruvate dehydrogenase E2 deficiency",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "LP:1 US:1",
      "phenotype_combined": "Pyruvate dehydrogenase E2 deficiency",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}