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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: 1-155659923-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=155659923&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 155659923,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000355499.9",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "NM_139119.3",
          "protein_id": "NP_620830.1",
          "transcript_support_level": null,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2254,
          "cdna_end": null,
          "cdna_length": 2723,
          "mane_select": "ENST00000355499.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "ENST00000355499.9",
          "protein_id": "ENSP00000347686.4",
          "transcript_support_level": 1,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2254,
          "cdna_end": null,
          "cdna_length": 2723,
          "mane_select": "NM_139119.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2341G>C",
          "hgvs_p": "p.Glu781Gln",
          "transcript": "ENST00000368340.10",
          "protein_id": "ENSP00000357324.5",
          "transcript_support_level": 1,
          "aa_start": 781,
          "aa_end": null,
          "aa_length": 868,
          "cds_start": 2341,
          "cds_end": null,
          "cds_length": 2607,
          "cdna_start": 2547,
          "cdna_end": null,
          "cdna_length": 3024,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "ENST00000347088.9",
          "protein_id": "ENSP00000316079.6",
          "transcript_support_level": 1,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2047,
          "cdna_end": null,
          "cdna_length": 2524,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "ENST00000368330.6",
          "protein_id": "ENSP00000357314.2",
          "transcript_support_level": 1,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2078,
          "cdna_end": null,
          "cdna_length": 2555,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1954G>C",
          "hgvs_p": "p.Glu652Gln",
          "transcript": "ENST00000359205.9",
          "protein_id": "ENSP00000352134.5",
          "transcript_support_level": 1,
          "aa_start": 652,
          "aa_end": null,
          "aa_length": 739,
          "cds_start": 1954,
          "cds_end": null,
          "cds_length": 2220,
          "cdna_start": 2213,
          "cdna_end": null,
          "cdna_length": 2690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1954G>C",
          "hgvs_p": "p.Glu652Gln",
          "transcript": "ENST00000361831.9",
          "protein_id": "ENSP00000355298.5",
          "transcript_support_level": 1,
          "aa_start": 652,
          "aa_end": null,
          "aa_length": 739,
          "cds_start": 1954,
          "cds_end": null,
          "cds_length": 2220,
          "cdna_start": 2266,
          "cdna_end": null,
          "cdna_length": 2743,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1927G>C",
          "hgvs_p": "p.Glu643Gln",
          "transcript": "ENST00000404643.5",
          "protein_id": "ENSP00000385390.1",
          "transcript_support_level": 1,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 730,
          "cds_start": 1927,
          "cds_end": null,
          "cds_length": 2193,
          "cdna_start": 2177,
          "cdna_end": null,
          "cdna_length": 2654,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "n.*1485G>C",
          "hgvs_p": null,
          "transcript": "ENST00000361140.8",
          "protein_id": "ENSP00000354716.4",
          "transcript_support_level": 1,
          "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": 2701,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "n.*1996G>C",
          "hgvs_p": null,
          "transcript": "ENST00000436865.5",
          "protein_id": "ENSP00000390116.1",
          "transcript_support_level": 1,
          "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": 2684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "n.*1485G>C",
          "hgvs_p": null,
          "transcript": "ENST00000361140.8",
          "protein_id": "ENSP00000354716.4",
          "transcript_support_level": 1,
          "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": 2701,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "n.*1996G>C",
          "hgvs_p": null,
          "transcript": "ENST00000436865.5",
          "protein_id": "ENSP00000390116.1",
          "transcript_support_level": 1,
          "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": 2684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2401G>C",
          "hgvs_p": "p.Glu801Gln",
          "transcript": "NM_001198903.1",
          "protein_id": "NP_001185832.1",
          "transcript_support_level": null,
          "aa_start": 801,
          "aa_end": null,
          "aa_length": 888,
          "cds_start": 2401,
          "cds_end": null,
          "cds_length": 2667,
          "cdna_start": 2593,
          "cdna_end": null,
          "cdna_length": 3074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2401G>C",
          "hgvs_p": "p.Glu801Gln",
          "transcript": "ENST00000368339.10",
          "protein_id": "ENSP00000357323.5",
          "transcript_support_level": 2,
          "aa_start": 801,
          "aa_end": null,
          "aa_length": 888,
          "cds_start": 2401,
          "cds_end": null,
          "cds_length": 2667,
          "cdna_start": 2597,
          "cdna_end": null,
          "cdna_length": 3065,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2341G>C",
          "hgvs_p": "p.Glu781Gln",
          "transcript": "NM_001198904.1",
          "protein_id": "NP_001185833.1",
          "transcript_support_level": null,
          "aa_start": 781,
          "aa_end": null,
          "aa_length": 868,
          "cds_start": 2341,
          "cds_end": null,
          "cds_length": 2607,
          "cdna_start": 2533,
          "cdna_end": null,
          "cdna_length": 3014,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2185G>C",
          "hgvs_p": "p.Glu729Gln",
          "transcript": "ENST00000715146.1",
          "protein_id": "ENSP00000520347.1",
          "transcript_support_level": null,
          "aa_start": 729,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2185,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2543,
          "cdna_end": null,
          "cdna_length": 2965,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2125G>C",
          "hgvs_p": "p.Glu709Gln",
          "transcript": "NM_139118.3",
          "protein_id": "NP_620829.1",
          "transcript_support_level": null,
          "aa_start": 709,
          "aa_end": null,
          "aa_length": 796,
          "cds_start": 2125,
          "cds_end": null,
          "cds_length": 2391,
          "cdna_start": 2145,
          "cdna_end": null,
          "cdna_length": 2614,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.2125G>C",
          "hgvs_p": "p.Glu709Gln",
          "transcript": "ENST00000295566.8",
          "protein_id": "ENSP00000295566.4",
          "transcript_support_level": 2,
          "aa_start": 709,
          "aa_end": null,
          "aa_length": 796,
          "cds_start": 2125,
          "cds_end": null,
          "cds_length": 2391,
          "cdna_start": 2149,
          "cdna_end": null,
          "cdna_length": 2626,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "NM_001198901.2",
          "protein_id": "NP_001185830.1",
          "transcript_support_level": null,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2074,
          "cdna_end": null,
          "cdna_length": 2543,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "YY1AP1",
          "gene_hgnc_id": 30935,
          "hgvs_c": "c.1987G>C",
          "hgvs_p": "p.Glu663Gln",
          "transcript": "NM_001198902.2",
          "protein_id": "NP_001185831.1",
          "transcript_support_level": null,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 1987,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 2123,
          "cdna_end": null,
          "cdna_length": 2592,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
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