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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: 11-118520660-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=118520660&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 118520660,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_001197104.2",
      "consequences": [
        {
          "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": 36,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11430-142A>G",
          "hgvs_p": null,
          "transcript": "NM_001197104.2",
          "protein_id": "NP_001184033.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3972,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11919,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16600,
          "mane_select": "ENST00000534358.8",
          "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": 36,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11430-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000534358.8",
          "protein_id": "ENSP00000436786.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3972,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11919,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16600,
          "mane_select": "NM_001197104.2",
          "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": 36,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11421-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000389506.10",
          "protein_id": "ENSP00000374157.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3969,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11910,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 13678,
          "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": 37,
          "intron_rank": 34,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11529-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000531904.7",
          "protein_id": "ENSP00000432391.3",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 4005,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 12018,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16699,
          "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": 37,
          "intron_rank": 34,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11520-142A>G",
          "hgvs_p": null,
          "transcript": "NM_001412597.1",
          "protein_id": "NP_001399526.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 4002,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 12009,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16690,
          "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": 37,
          "intron_rank": 34,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11520-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000710560.1",
          "protein_id": "ENSP00000518343.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 4002,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 12009,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16725,
          "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": 37,
          "intron_rank": 34,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11502-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000691053.1",
          "protein_id": "ENSP00000509168.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3996,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11991,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 13708,
          "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": 36,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11421-142A>G",
          "hgvs_p": null,
          "transcript": "NM_005933.4",
          "protein_id": "NP_005924.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3969,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11910,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 16591,
          "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": 35,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "c.11307-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000649699.1",
          "protein_id": "ENSP00000496927.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 3931,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 11796,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11796,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "n.345-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000525408.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 857,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.136+586T>C",
          "hgvs_p": null,
          "transcript": "ENST00000525992.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 448,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "n.930-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000527839.2",
          "protein_id": null,
          "transcript_support_level": 3,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4823,
          "mane_select": null,
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          "feature": null
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.222+606T>C",
          "hgvs_p": null,
          "transcript": "ENST00000528578.5",
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 3,
          "intron_rank": 2,
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          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.241+606T>C",
          "hgvs_p": null,
          "transcript": "ENST00000532597.6",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2069,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.321+606T>C",
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          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.200+606T>C",
          "hgvs_p": null,
          "transcript": "ENST00000556583.2",
          "protein_id": null,
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          "cds_start": -4,
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          "cdna_length": 512,
          "mane_select": null,
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        {
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          "canonical": false,
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          "strand": true,
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "n.666-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648565.1",
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          "cdna_length": 1851,
          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "KMT2A",
          "gene_hgnc_id": 7132,
          "hgvs_c": "n.*11-142A>G",
          "hgvs_p": null,
          "transcript": "ENST00000686588.1",
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          "gene_symbol": "TTC36-AS1",
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          "hgvs_c": "n.200+606T>C",
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          "transcript": "ENST00000719865.1",
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          "exon_count": 3,
          "intron_rank": 2,
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          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.178+606T>C",
          "hgvs_p": null,
          "transcript": "ENST00000719866.1",
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          "cdna_length": 364,
          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TTC36-AS1",
          "gene_hgnc_id": 55495,
          "hgvs_c": "n.428+606T>C",
          "hgvs_p": null,
          "transcript": "NR_120572.1",
          "protein_id": null,
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      ],
      "gene_symbol": "KMT2A",
      "gene_hgnc_id": 7132,
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      "frequency_reference_population": 0.3550315,
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      "gnomad_exomes_af": 0.36847,
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      "gnomad_genomes_homalt": 9220,
      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": -0.9300000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": null,
      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.93,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.247,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "mitotip_score": null,
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      "acmg_score": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BA1",
      "acmg_by_gene": [
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          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_001197104.2",
          "gene_symbol": "KMT2A",
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          ],
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        {
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          "pathogenic_score": 0,
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            "BP4_Strong",
            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000532597.6",
          "gene_symbol": "TTC36-AS1",
          "hgnc_id": 55495,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.241+606T>C",
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}