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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: 18-34875316-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=34875316&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "18",
      "pos": 34875316,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001386788.1",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1821G>T",
          "hgvs_p": "p.Ala607Ala",
          "transcript": "NM_001386795.1",
          "protein_id": "NP_001373724.1",
          "transcript_support_level": null,
          "aa_start": 607,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": 1821,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000444659.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386795.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1821G>T",
          "hgvs_p": "p.Ala607Ala",
          "transcript": "ENST00000444659.6",
          "protein_id": "ENSP00000405819.2",
          "transcript_support_level": 5,
          "aa_start": 607,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": 1821,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001386795.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000444659.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1560G>T",
          "hgvs_p": "p.Ala520Ala",
          "transcript": "ENST00000598334.5",
          "protein_id": "ENSP00000470152.1",
          "transcript_support_level": 1,
          "aa_start": 520,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1560,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000598334.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1581G>T",
          "hgvs_p": "p.Ala527Ala",
          "transcript": "ENST00000399121.9",
          "protein_id": "ENSP00000382072.5",
          "transcript_support_level": 1,
          "aa_start": 527,
          "aa_end": null,
          "aa_length": 690,
          "cds_start": 1581,
          "cds_end": null,
          "cds_length": 2073,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000399121.9"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1569G>T",
          "hgvs_p": "p.Ala523Ala",
          "transcript": "ENST00000598142.5",
          "protein_id": "ENSP00000470716.1",
          "transcript_support_level": 1,
          "aa_start": 523,
          "aa_end": null,
          "aa_length": 686,
          "cds_start": 1569,
          "cds_end": null,
          "cds_length": 2061,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000598142.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1560G>T",
          "hgvs_p": "p.Ala520Ala",
          "transcript": "ENST00000595022.5",
          "protein_id": "ENSP00000473078.1",
          "transcript_support_level": 1,
          "aa_start": 520,
          "aa_end": null,
          "aa_length": 683,
          "cds_start": 1560,
          "cds_end": null,
          "cds_length": 2052,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000595022.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.684G>T",
          "hgvs_p": "p.Ala228Ala",
          "transcript": "ENST00000591182.5",
          "protein_id": "ENSP00000467720.1",
          "transcript_support_level": 1,
          "aa_start": 228,
          "aa_end": null,
          "aa_length": 391,
          "cds_start": 684,
          "cds_end": null,
          "cds_length": 1176,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000591182.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1821G>T",
          "hgvs_p": "p.Ala607Ala",
          "transcript": "NM_001386788.1",
          "protein_id": "NP_001373717.1",
          "transcript_support_level": null,
          "aa_start": 607,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": 1821,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386788.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1821G>T",
          "hgvs_p": "p.Ala607Ala",
          "transcript": "ENST00000679796.1",
          "protein_id": "ENSP00000506659.1",
          "transcript_support_level": null,
          "aa_start": 607,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": 1821,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000679796.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1752G>T",
          "hgvs_p": "p.Ala584Ala",
          "transcript": "ENST00000970105.1",
          "protein_id": "ENSP00000640164.1",
          "transcript_support_level": null,
          "aa_start": 584,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 1752,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000970105.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1740G>T",
          "hgvs_p": "p.Ala580Ala",
          "transcript": "NM_001390.5",
          "protein_id": "NP_001381.2",
          "transcript_support_level": null,
          "aa_start": 580,
          "aa_end": null,
          "aa_length": 743,
          "cds_start": 1740,
          "cds_end": null,
          "cds_length": 2232,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001390.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1740G>T",
          "hgvs_p": "p.Ala580Ala",
          "transcript": "ENST00000399113.7",
          "protein_id": "ENSP00000382064.3",
          "transcript_support_level": 5,
          "aa_start": 580,
          "aa_end": null,
          "aa_length": 743,
          "cds_start": 1740,
          "cds_end": null,
          "cds_length": 2232,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000399113.7"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1560G>T",
          "hgvs_p": "p.Ala520Ala",
          "transcript": "NM_001198938.2",
          "protein_id": "NP_001185867.1",
          "transcript_support_level": null,
          "aa_start": 520,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1560,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001198938.2"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1560G>T",
          "hgvs_p": "p.Ala520Ala",
          "transcript": "NM_001386753.1",
          "protein_id": "NP_001373682.1",
          "transcript_support_level": null,
          "aa_start": 520,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 1560,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386753.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386754.1",
          "protein_id": "NP_001373683.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386754.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386755.1",
          "protein_id": "NP_001373684.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386755.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386756.1",
          "protein_id": "NP_001373685.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386756.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386757.1",
          "protein_id": "NP_001373686.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386757.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386758.1",
          "protein_id": "NP_001373687.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386758.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DTNA",
          "gene_hgnc_id": 3057,
          "hgvs_c": "c.1650G>T",
          "hgvs_p": "p.Ala550Ala",
          "transcript": "NM_001386759.1",
          "protein_id": "NP_001373688.1",
          "transcript_support_level": null,
          "aa_start": 550,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1650,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001386759.1"
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      "gene_symbol": "DTNA",
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      "dbsnp": "rs9959365",
      "frequency_reference_population": 0.000008054283,
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      "allele_count_reference_population": 13,
      "gnomad_exomes_af": 0.00000820865,
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      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8500000238418579,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
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      "revel_score": null,
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.85,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -3.1,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
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      "acmg_score": -17,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -17,
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          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Very_Strong",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001386788.1",
          "gene_symbol": "DTNA",
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          "effects": [
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          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1821G>T",
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      ],
      "clinvar_disease": "Left ventricular noncompaction 1,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "not specified|Left ventricular noncompaction 1",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}