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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: 16-23348878-T-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=23348878&ref=T&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 5,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "SCNN1B",
          "hgnc_id": 10600,
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "inheritance_mode": "AD,AR,SD",
          "pathogenic_score": 2,
          "score": -3,
          "transcript": "NM_000336.3",
          "verdict": "Likely_benign"
        }
      ],
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_score": -3,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.7,
      "chr": "16",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.699999988079071,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2560,
          "cdna_start": 423,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "NM_000336.3",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000343070.7",
          "protein_coding": true,
          "protein_id": "NP_000327.2",
          "strand": true,
          "transcript": "NM_000336.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 2560,
          "cdna_start": 423,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000343070.7",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_000336.3",
          "protein_coding": true,
          "protein_id": "ENSP00000345751.2",
          "strand": true,
          "transcript": "ENST00000343070.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 685,
          "aa_ref": "P",
          "aa_start": 138,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2085,
          "cdna_start": 441,
          "cds_end": null,
          "cds_length": 2058,
          "cds_start": 414,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000307331.9",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.414T>A",
          "hgvs_p": "p.Pro138Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000302874.5",
          "strand": true,
          "transcript": "ENST00000307331.9",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 672,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2628,
          "cdna_start": 397,
          "cds_end": null,
          "cds_length": 2019,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000962247.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632306.1",
          "strand": true,
          "transcript": "ENST00000962247.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2618,
          "cdna_start": 476,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000890249.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560308.1",
          "strand": true,
          "transcript": "ENST00000890249.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2693,
          "cdna_start": 559,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000890250.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560309.1",
          "strand": true,
          "transcript": "ENST00000890250.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2674,
          "cdna_start": 536,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000890252.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560311.1",
          "strand": true,
          "transcript": "ENST00000890252.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2540,
          "cdna_start": 409,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000890258.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560317.1",
          "strand": true,
          "transcript": "ENST00000890258.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2590,
          "cdna_start": 455,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000890259.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560318.1",
          "strand": true,
          "transcript": "ENST00000890259.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2613,
          "cdna_start": 471,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000928026.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598085.1",
          "strand": true,
          "transcript": "ENST00000928026.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2621,
          "cdna_start": 479,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000928027.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598086.1",
          "strand": true,
          "transcript": "ENST00000928027.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 640,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2650,
          "cdna_start": 515,
          "cds_end": null,
          "cds_length": 1923,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000962248.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632307.1",
          "strand": true,
          "transcript": "ENST00000962248.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 639,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2515,
          "cdna_start": 380,
          "cds_end": null,
          "cds_length": 1920,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000890257.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560316.1",
          "strand": true,
          "transcript": "ENST00000890257.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 637,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2559,
          "cdna_start": 431,
          "cds_end": null,
          "cds_length": 1914,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000890251.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000560310.1",
          "strand": true,
          "transcript": "ENST00000890251.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 637,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2562,
          "cdna_start": 431,
          "cds_end": null,
          "cds_length": 1914,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000928028.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598087.1",
          "strand": true,
          "transcript": "ENST00000928028.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 637,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2575,
          "cdna_start": 448,
          "cds_end": null,
          "cds_length": 1914,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000962244.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632303.1",
          "strand": true,
          "transcript": "ENST00000962244.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 632,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2510,
          "cdna_start": 400,
          "cds_end": null,
          "cds_length": 1899,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 13,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000962246.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632305.1",
          "strand": true,
          "transcript": "ENST00000962246.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 613,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1852,
          "cdna_start": 287,
          "cds_end": null,
          "cds_length": 1842,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 12,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000568923.5",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000456309.1",
          "strand": true,
          "transcript": "ENST00000568923.5",
          "transcript_support_level": 3
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 604,
          "aa_ref": "P",
          "aa_start": 93,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2452,
          "cdna_start": 423,
          "cds_end": null,
          "cds_length": 1815,
          "cds_start": 279,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 12,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "NM_001410900.1",
          "gene_hgnc_id": 10600,
          "gene_symbol": "SCNN1B",
          "hgvs_c": "c.279T>A",
          "hgvs_p": "p.Pro93Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
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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.