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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: 11-118436575-C-CG (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=118436575&ref=C&alt=CG&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 118436575,
      "ref": "C",
      "alt": "CG",
      "effect": "frameshift_variant",
      "transcript": "NM_001197104.2",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "NM_001197104.2",
          "protein_id": "NP_001184033.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3972,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 11919,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 16600,
          "mane_select": "ENST00000534358.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000534358.8",
          "protein_id": "ENSP00000436786.2",
          "transcript_support_level": 1,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3972,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 11919,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 16600,
          "mane_select": "NM_001197104.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000389506.10",
          "protein_id": "ENSP00000374157.5",
          "transcript_support_level": 1,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3969,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 11910,
          "cdna_start": 93,
          "cdna_end": null,
          "cdna_length": 13678,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000285827",
          "gene_hgnc_id": null,
          "hgvs_c": "c.-798-32194dupG",
          "hgvs_p": null,
          "transcript": "ENST00000648261.1",
          "protein_id": "ENSP00000498126.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 929,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2790,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000531904.7",
          "protein_id": "ENSP00000432391.3",
          "transcript_support_level": 2,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 4005,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 12018,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 16699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "NM_001412597.1",
          "protein_id": "NP_001399526.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 4002,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 12009,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 16690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000710560.1",
          "protein_id": "ENSP00000518343.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 4002,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 12009,
          "cdna_start": 126,
          "cdna_end": null,
          "cdna_length": 16725,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000691053.1",
          "protein_id": "ENSP00000509168.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3996,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 11991,
          "cdna_start": 78,
          "cdna_end": null,
          "cdna_length": 13708,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "NM_005933.4",
          "protein_id": "NP_005924.2",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3969,
          "cds_start": 70,
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          "cds_length": 11910,
          "cdna_start": 91,
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          "cdna_length": 16591,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000649699.1",
          "protein_id": "ENSP00000496927.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3931,
          "cds_start": 70,
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          "cds_length": 11796,
          "cdna_start": 70,
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          "cdna_length": 11796,
          "mane_select": null,
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "KMT2A",
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          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000649690.2",
          "protein_id": "ENSP00000497372.2",
          "transcript_support_level": null,
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          "cds_start": 70,
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          "cdna_start": 91,
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          "cdna_length": 1840,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "KMT2A",
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          "hgvs_p": "p.Arg24fs",
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        {
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          "intron_rank": null,
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          "gene_symbol": "KMT2A",
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          "transcript": "ENST00000533790.3",
          "protein_id": "ENSP00000436700.3",
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        {
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          "intron_rank": null,
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          "gene_symbol": "KMT2A",
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          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000649666.2",
          "protein_id": "ENSP00000497918.2",
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          "cds_length": 594,
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          "mane_select": null,
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        },
        {
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          ],
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          "gene_symbol": "KMT2A",
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "ENST00000532204.6",
          "protein_id": "ENSP00000434618.2",
          "transcript_support_level": 2,
          "aa_start": 24,
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          "cdna_start": 91,
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          "biotype": null,
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        {
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          "exon_count": 37,
          "intron_rank": null,
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          "gene_symbol": "KMT2A",
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          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "XM_011542829.3",
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        },
        {
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          ],
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          "gene_symbol": "KMT2A",
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          "hgvs_c": "c.69dupG",
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        {
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          "gene_symbol": "KMT2A",
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        {
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          ],
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          "gene_symbol": "KMT2A",
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          "hgvs_c": "c.69dupG",
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          "transcript": "XM_011542833.3",
          "protein_id": "XP_011541135.1",
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          "cds_start": 70,
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          "cdna_length": 14182,
          "mane_select": null,
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        },
        {
          "aa_ref": "R",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "XM_006718839.4",
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          "aa_start": 24,
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          "aa_length": 3133,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 9402,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 14083,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "A?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs",
          "transcript": "XM_047426964.1",
          "protein_id": "XP_047282920.1",
          "transcript_support_level": null,
          "aa_start": 24,
          "aa_end": null,
          "aa_length": 3130,
          "cds_start": 70,
          "cds_end": null,
          "cds_length": 9393,
          "cdna_start": 91,
          "cdna_end": null,
          "cdna_length": 14074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000285827",
          "gene_hgnc_id": null,
          "hgvs_c": "c.214-11044dupG",
          "hgvs_p": null,
          "transcript": "ENST00000649464.1",
          "protein_id": "ENSP00000497966.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 91,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 276,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2222,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "KMT2A",
      "gene_hgnc_id": 7132,
      "dbsnp": "rs2134152310",
      "frequency_reference_population": 0.000006934758,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 7,
      "gnomad_exomes_af": 0.00000693476,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 7,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "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": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": -0.289,
      "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": 8,
      "acmg_classification": "Likely_pathogenic",
      "acmg_criteria": "PVS1",
      "acmg_by_gene": [
        {
          "score": 8,
          "benign_score": 0,
          "pathogenic_score": 8,
          "criteria": [
            "PVS1"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "NM_001197104.2",
          "gene_symbol": "KMT2A",
          "hgnc_id": 7132,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.69dupG",
          "hgvs_p": "p.Arg24fs"
        },
        {
          "score": 2,
          "benign_score": 0,
          "pathogenic_score": 2,
          "criteria": [
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000648261.1",
          "gene_symbol": "ENSG00000285827",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.-798-32194dupG",
          "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
}