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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: 19-11576377-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=11576377&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 21,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1",
            "BS2"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "ACP5",
          "hgnc_id": 124,
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": -21,
          "transcript": "NM_001611.5",
          "verdict": "Benign"
        },
        {
          "benign_score": 16,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "ZNF627",
          "hgnc_id": 30570,
          "hgvs_c": "c.-94+1024G>A",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": -16,
          "transcript": "ENST00000585493.5",
          "verdict": "Benign"
        },
        {
          "benign_score": 16,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "LOC124904638",
          "hgnc_id": null,
          "hgvs_c": "n.105+1024G>A",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": -16,
          "transcript": "XR_007067140.1",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
      "acmg_score": -21,
      "allele_count_reference_population": 567,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.54,
      "chr": "19",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_disease": "Spondyloenchondrodysplasia with immune dysregulation,not provided",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:1 B:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.5400000214576721,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1381,
          "cdna_start": 654,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001611.5",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000648477.1",
          "protein_coding": true,
          "protein_id": "NP_001602.1",
          "strand": false,
          "transcript": "NM_001611.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1381,
          "cdna_start": 654,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000648477.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001611.5",
          "protein_coding": true,
          "protein_id": "ENSP00000496973.1",
          "strand": false,
          "transcript": "ENST00000648477.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1752,
          "cdna_start": 1025,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000218758.10",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000218758.4",
          "strand": false,
          "transcript": "ENST00000218758.10",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 333,
          "aa_ref": "L",
          "aa_start": 209,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1437,
          "cdna_start": 712,
          "cds_end": null,
          "cds_length": 1002,
          "cds_start": 625,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000889667.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.625C>T",
          "hgvs_p": "p.Leu209Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000559726.1",
          "strand": false,
          "transcript": "ENST00000889667.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1571,
          "cdna_start": 844,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001111034.3",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001104504.1",
          "strand": false,
          "transcript": "NM_001111034.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1620,
          "cdna_start": 893,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "NM_001111035.3",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001104505.1",
          "strand": false,
          "transcript": "NM_001111035.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1547,
          "cdna_start": 820,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001111036.3",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001104506.1",
          "strand": false,
          "transcript": "NM_001111036.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1649,
          "cdna_start": 922,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_001322023.2",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001308952.1",
          "strand": false,
          "transcript": "NM_001322023.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1727,
          "cdna_start": 1000,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "NM_001439233.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001426162.1",
          "strand": false,
          "transcript": "NM_001439233.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1725,
          "cdna_start": 998,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "NM_001439234.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001426163.1",
          "strand": false,
          "transcript": "NM_001439234.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1791,
          "cdna_start": 1064,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 8,
          "exon_rank": 7,
          "exon_rank_end": null,
          "feature": "NM_001439235.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001426164.1",
          "strand": false,
          "transcript": "NM_001439235.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1898,
          "cdna_start": 1171,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 8,
          "exon_rank": 7,
          "exon_rank_end": null,
          "feature": "NM_001439236.1",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001426165.1",
          "strand": false,
          "transcript": "NM_001439236.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1602,
          "cdna_start": 875,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000412435.7",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000392374.1",
          "strand": false,
          "transcript": "ENST00000412435.7",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1727,
          "cdna_start": 1000,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 8,
          "exon_rank": 7,
          "exon_rank_end": null,
          "feature": "ENST00000589792.6",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000468685.2",
          "strand": false,
          "transcript": "ENST00000589792.6",
          "transcript_support_level": 3
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1538,
          "cdna_start": 811,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 4,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000590832.2",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000465127.2",
          "strand": false,
          "transcript": "ENST00000590832.2",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1751,
          "cdna_start": 1024,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000591319.2",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000464831.2",
          "strand": false,
          "transcript": "ENST00000591319.2",
          "transcript_support_level": 3
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2114,
          "cdna_start": 1387,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000592659.2",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000465498.2",
          "strand": false,
          "transcript": "ENST00000592659.2",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 325,
          "aa_ref": "L",
          "aa_start": 201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1746,
          "cdna_start": 1012,
          "cds_end": null,
          "cds_length": 978,
          "cds_start": 601,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000592828.7",
          "gene_hgnc_id": 124,
          "gene_symbol": "ACP5",
          "hgvs_c": "c.601C>T",
          "hgvs_p": "p.Leu201Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": 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.