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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: 16-56497063-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=56497063&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 56497063,
      "ref": "G",
      "alt": "C",
      "effect": "stop_gained",
      "transcript": "NM_031885.5",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "NM_031885.5",
          "protein_id": "NP_114091.4",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000245157.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_031885.5"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000245157.11",
          "protein_id": "ENSP00000245157.5",
          "transcript_support_level": 1,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_031885.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000245157.11"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "n.5345C>G",
          "hgvs_p": null,
          "transcript": "ENST00000565781.6",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000565781.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000288725",
          "gene_hgnc_id": null,
          "hgvs_c": "n.734C>G",
          "hgvs_p": null,
          "transcript": "ENST00000684388.1",
          "protein_id": "ENSP00000507647.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000684388.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1859C>G",
          "hgvs_p": "p.Ser620*",
          "transcript": "ENST00000682188.1",
          "protein_id": "ENSP00000507655.1",
          "transcript_support_level": null,
          "aa_start": 620,
          "aa_end": null,
          "aa_length": 736,
          "cds_start": 1859,
          "cds_end": null,
          "cds_length": 2211,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682188.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "NM_001377456.1",
          "protein_id": "NP_001364385.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001377456.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000682047.1",
          "protein_id": "ENSP00000507699.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682047.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000682205.1",
          "protein_id": "ENSP00000508377.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682205.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000682470.1",
          "protein_id": "ENSP00000507654.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682470.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000682855.1",
          "protein_id": "ENSP00000507027.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682855.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1814C>G",
          "hgvs_p": "p.Ser605*",
          "transcript": "ENST00000854960.1",
          "protein_id": "ENSP00000525019.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1814,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000854960.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1802C>G",
          "hgvs_p": "p.Ser601*",
          "transcript": "ENST00000966325.1",
          "protein_id": "ENSP00000636384.1",
          "transcript_support_level": null,
          "aa_start": 601,
          "aa_end": null,
          "aa_length": 717,
          "cds_start": 1802,
          "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": "ENST00000966325.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1781C>G",
          "hgvs_p": "p.Ser594*",
          "transcript": "ENST00000854962.1",
          "protein_id": "ENSP00000525021.1",
          "transcript_support_level": null,
          "aa_start": 594,
          "aa_end": null,
          "aa_length": 710,
          "cds_start": 1781,
          "cds_end": null,
          "cds_length": 2133,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000854962.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1778C>G",
          "hgvs_p": "p.Ser593*",
          "transcript": "ENST00000854961.1",
          "protein_id": "ENSP00000525020.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 709,
          "cds_start": 1778,
          "cds_end": null,
          "cds_length": 2130,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000854961.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1766C>G",
          "hgvs_p": "p.Ser589*",
          "transcript": "ENST00000683858.1",
          "protein_id": "ENSP00000507657.1",
          "transcript_support_level": null,
          "aa_start": 589,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": 1766,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000683858.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1745C>G",
          "hgvs_p": "p.Ser582*",
          "transcript": "ENST00000923962.1",
          "protein_id": "ENSP00000594021.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 698,
          "cds_start": 1745,
          "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": "ENST00000923962.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1745C>G",
          "hgvs_p": "p.Ser582*",
          "transcript": "ENST00000923963.1",
          "protein_id": "ENSP00000594022.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 698,
          "cds_start": 1745,
          "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": "ENST00000923963.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1739C>G",
          "hgvs_p": "p.Ser580*",
          "transcript": "ENST00000682930.1",
          "protein_id": "ENSP00000507981.1",
          "transcript_support_level": null,
          "aa_start": 580,
          "aa_end": null,
          "aa_length": 696,
          "cds_start": 1739,
          "cds_end": null,
          "cds_length": 2091,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000682930.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1709C>G",
          "hgvs_p": "p.Ser570*",
          "transcript": "ENST00000684635.1",
          "protein_id": "ENSP00000507335.1",
          "transcript_support_level": null,
          "aa_start": 570,
          "aa_end": null,
          "aa_length": 686,
          "cds_start": 1709,
          "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": "ENST00000684635.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS2",
          "gene_hgnc_id": 967,
          "hgvs_c": "c.1709C>G",
          "hgvs_p": "p.Ser570*",
          "transcript": "ENST00000966324.1",
          "protein_id": "ENSP00000636383.1",
          "transcript_support_level": null,
          "aa_start": 570,
          "aa_end": null,
          "aa_length": 686,
          "cds_start": 1709,
          "cds_end": null,
          "cds_length": 2061,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "gene_symbol": "ENSG00000288725",
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      "clinvar_disease": "Bardet-Biedl syndrome,Bardet-Biedl syndrome 2,Retinitis pigmentosa 74",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:3",
      "phenotype_combined": "Bardet-Biedl syndrome 2|Bardet-Biedl syndrome|Retinitis pigmentosa 74;Bardet-Biedl syndrome 2",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
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  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.