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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: 16-74906468-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=74906468&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 12,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "WDR59",
          "hgnc_id": 25706,
          "hgvs_c": "c.1713-2368G>T",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": -12,
          "transcript": "NM_030581.4",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_score": -12,
      "allele_count_reference_population": 76315,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.95,
      "chr": "16",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.949999988079071,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 974,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5878,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2925,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_030581.4",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1713-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000262144.11",
          "protein_coding": true,
          "protein_id": "NP_085058.3",
          "strand": false,
          "transcript": "NM_030581.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 974,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5878,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2925,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000262144.11",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1713-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_030581.4",
          "protein_coding": true,
          "protein_id": "ENSP00000262144.6",
          "strand": false,
          "transcript": "ENST00000262144.11",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1022,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3816,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3069,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000857980.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1857-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000528039.1",
          "strand": false,
          "transcript": "ENST00000857980.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1013,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3739,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3042,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 27,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918564.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1830-2368G>T",
          "hgvs_p": null,
          "intron_rank": 18,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588623.1",
          "strand": false,
          "transcript": "ENST00000918564.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1011,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3767,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3036,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 27,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918559.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1824-2368G>T",
          "hgvs_p": null,
          "intron_rank": 18,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588618.1",
          "strand": false,
          "transcript": "ENST00000918559.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 992,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3695,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2979,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 27,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918561.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1767-2368G>T",
          "hgvs_p": null,
          "intron_rank": 18,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588620.1",
          "strand": false,
          "transcript": "ENST00000918561.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 972,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3651,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2919,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956303.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1707-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626362.1",
          "strand": false,
          "transcript": "ENST00000956303.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 965,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3615,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2898,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956304.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1686-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626363.1",
          "strand": false,
          "transcript": "ENST00000956304.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 957,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3607,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2874,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000857982.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1662-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000528041.1",
          "strand": false,
          "transcript": "ENST00000857982.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 948,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3579,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2847,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 25,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956302.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1635-2368G>T",
          "hgvs_p": null,
          "intron_rank": 16,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626361.1",
          "strand": false,
          "transcript": "ENST00000956302.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 946,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3539,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2841,
          "cds_start": null,
          "consequences": [
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          ],
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          "exon_rank": null,
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          "feature": "ENST00000918563.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1629-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588622.1",
          "strand": false,
          "transcript": "ENST00000918563.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 942,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3591,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2829,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 25,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918556.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1617-2368G>T",
          "hgvs_p": null,
          "intron_rank": 16,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588615.1",
          "strand": false,
          "transcript": "ENST00000918556.1",
          "transcript_support_level": null
        },
        {
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          "aa_length": 941,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3565,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2826,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000857981.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1614-2368G>T",
          "hgvs_p": null,
          "intron_rank": 17,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000528040.1",
          "strand": false,
          "transcript": "ENST00000857981.1",
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        },
        {
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          "biotype": "protein_coding",
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          "cdna_length": 3525,
          "cdna_start": null,
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          "consequences": [
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          ],
          "exon_count": 25,
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          "feature": "ENST00000857983.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1596-2368G>T",
          "hgvs_p": null,
          "intron_rank": 16,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000528042.1",
          "strand": false,
          "transcript": "ENST00000857983.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 909,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3463,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2730,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 25,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918557.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1518-2368G>T",
          "hgvs_p": null,
          "intron_rank": 16,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588616.1",
          "strand": false,
          "transcript": "ENST00000918557.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 900,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3382,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2703,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 24,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918565.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1491-2368G>T",
          "hgvs_p": null,
          "intron_rank": 15,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588624.1",
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          "transcript": "ENST00000918565.1",
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        },
        {
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          "aa_ref": null,
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          "cdna_length": 3396,
          "cdna_start": null,
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          "cds_length": 2664,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 24,
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          "feature": "ENST00000918558.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1452-2368G>T",
          "hgvs_p": null,
          "intron_rank": 15,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588617.1",
          "strand": false,
          "transcript": "ENST00000918558.1",
          "transcript_support_level": null
        },
        {
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          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
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          "cdna_length": 3158,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2448,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 22,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000918562.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.1389+5730G>T",
          "hgvs_p": null,
          "intron_rank": 14,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000588621.1",
          "strand": false,
          "transcript": "ENST00000918562.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 722,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2878,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2169,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 20,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000857984.1",
          "gene_hgnc_id": 25706,
          "gene_symbol": "WDR59",
          "hgvs_c": "c.957-2368G>T",
          "hgvs_p": null,
          "intron_rank": 11,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000528043.1",
          "strand": false,
          "transcript": "ENST00000857984.1",
          "transcript_support_level": null
        },
        {
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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.