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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: 14-105211174-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=105211174&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 105211174,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_001519.4",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1944C>T",
          "hgvs_p": "p.Asp648Asp",
          "transcript": "NM_001519.4",
          "protein_id": "NP_001510.2",
          "transcript_support_level": null,
          "aa_start": 648,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1944,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000547530.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001519.4"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1944C>T",
          "hgvs_p": "p.Asp648Asp",
          "transcript": "ENST00000547530.7",
          "protein_id": "ENSP00000448387.2",
          "transcript_support_level": 1,
          "aa_start": 648,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1944,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001519.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000547530.7"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1863C>T",
          "hgvs_p": "p.Asp621Asp",
          "transcript": "ENST00000379937.6",
          "protein_id": "ENSP00000369269.2",
          "transcript_support_level": 1,
          "aa_start": 621,
          "aa_end": null,
          "aa_length": 650,
          "cds_start": 1863,
          "cds_end": null,
          "cds_length": 1953,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000379937.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1332C>T",
          "hgvs_p": "p.Asp444Asp",
          "transcript": "ENST00000392557.8",
          "protein_id": "ENSP00000376340.4",
          "transcript_support_level": 1,
          "aa_start": 444,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 1332,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000392557.8"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.403-1515C>T",
          "hgvs_p": null,
          "transcript": "ENST00000551787.5",
          "protein_id": "ENSP00000446901.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 161,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 486,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000551787.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.2064C>T",
          "hgvs_p": "p.Asp688Asp",
          "transcript": "ENST00000910241.1",
          "protein_id": "ENSP00000580300.1",
          "transcript_support_level": null,
          "aa_start": 688,
          "aa_end": null,
          "aa_length": 717,
          "cds_start": 2064,
          "cds_end": null,
          "cds_length": 2154,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910241.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.2052C>T",
          "hgvs_p": "p.Asp684Asp",
          "transcript": "ENST00000910245.1",
          "protein_id": "ENSP00000580304.1",
          "transcript_support_level": null,
          "aa_start": 684,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 2052,
          "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": "ENST00000910245.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.2007C>T",
          "hgvs_p": "p.Asp669Asp",
          "transcript": "ENST00000910239.1",
          "protein_id": "ENSP00000580298.1",
          "transcript_support_level": null,
          "aa_start": 669,
          "aa_end": null,
          "aa_length": 698,
          "cds_start": 2007,
          "cds_end": null,
          "cds_length": 2097,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910239.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1941C>T",
          "hgvs_p": "p.Asp647Asp",
          "transcript": "NM_001440449.1",
          "protein_id": "NP_001427378.1",
          "transcript_support_level": null,
          "aa_start": 647,
          "aa_end": null,
          "aa_length": 676,
          "cds_start": 1941,
          "cds_end": null,
          "cds_length": 2031,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440449.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1941C>T",
          "hgvs_p": "p.Asp647Asp",
          "transcript": "ENST00000910238.1",
          "protein_id": "ENSP00000580297.1",
          "transcript_support_level": null,
          "aa_start": 647,
          "aa_end": null,
          "aa_length": 676,
          "cds_start": 1941,
          "cds_end": null,
          "cds_length": 2031,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910238.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1938C>T",
          "hgvs_p": "p.Asp646Asp",
          "transcript": "ENST00000910242.1",
          "protein_id": "ENSP00000580301.1",
          "transcript_support_level": null,
          "aa_start": 646,
          "aa_end": null,
          "aa_length": 675,
          "cds_start": 1938,
          "cds_end": null,
          "cds_length": 2028,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910242.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1863C>T",
          "hgvs_p": "p.Asp621Asp",
          "transcript": "NM_001242788.2",
          "protein_id": "NP_001229717.1",
          "transcript_support_level": null,
          "aa_start": 621,
          "aa_end": null,
          "aa_length": 650,
          "cds_start": 1863,
          "cds_end": null,
          "cds_length": 1953,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242788.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1860C>T",
          "hgvs_p": "p.Asp620Asp",
          "transcript": "ENST00000910240.1",
          "protein_id": "ENSP00000580299.1",
          "transcript_support_level": null,
          "aa_start": 620,
          "aa_end": null,
          "aa_length": 649,
          "cds_start": 1860,
          "cds_end": null,
          "cds_length": 1950,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910240.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1794C>T",
          "hgvs_p": "p.Asp598Asp",
          "transcript": "NM_001440450.1",
          "protein_id": "NP_001427379.1",
          "transcript_support_level": null,
          "aa_start": 598,
          "aa_end": null,
          "aa_length": 627,
          "cds_start": 1794,
          "cds_end": null,
          "cds_length": 1884,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440450.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Asp597Asp",
          "transcript": "ENST00000957204.1",
          "protein_id": "ENSP00000627263.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 626,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1881,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000957204.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1665C>T",
          "hgvs_p": "p.Asp555Asp",
          "transcript": "NM_001242786.2",
          "protein_id": "NP_001229715.1",
          "transcript_support_level": null,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242786.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1665C>T",
          "hgvs_p": "p.Asp555Asp",
          "transcript": "ENST00000440513.7",
          "protein_id": "ENSP00000388877.3",
          "transcript_support_level": 2,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000440513.7"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1599C>T",
          "hgvs_p": "p.Asp533Asp",
          "transcript": "NM_001242787.2",
          "protein_id": "NP_001229716.1",
          "transcript_support_level": null,
          "aa_start": 533,
          "aa_end": null,
          "aa_length": 562,
          "cds_start": 1599,
          "cds_end": null,
          "cds_length": 1689,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242787.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1599C>T",
          "hgvs_p": "p.Asp533Asp",
          "transcript": "ENST00000327359.7",
          "protein_id": "ENSP00000329029.3",
          "transcript_support_level": 2,
          "aa_start": 533,
          "aa_end": null,
          "aa_length": 562,
          "cds_start": 1599,
          "cds_end": null,
          "cds_length": 1689,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000327359.7"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRF1",
          "gene_hgnc_id": 11551,
          "hgvs_c": "c.1590C>T",
          "hgvs_p": "p.Asp530Asp",
          "transcript": "ENST00000910244.1",
          "protein_id": "ENSP00000580303.1",
          "transcript_support_level": null,
          "aa_start": 530,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1590,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000910244.1"
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      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -2.384,
      "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": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -7,
          "benign_score": 7,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Benign",
          "transcript": "NM_001519.4",
          "gene_symbol": "BRF1",
          "hgnc_id": 11551,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.1944C>T",
          "hgvs_p": "p.Asp648Asp"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}