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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: 12-14475135-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=14475135&ref=A&alt=G&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": "ATF7IP",
          "hgnc_id": 20092,
          "hgvs_c": "c.2887-755A>G",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": -12,
          "transcript": "NM_181352.2",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_score": -12,
      "allele_count_reference_population": 49813,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "G",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.99,
      "chr": "12",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.9900000095367432,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1270,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8823,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_018179.5",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000261168.9",
          "protein_coding": true,
          "protein_id": "NP_060649.3",
          "strand": true,
          "transcript": "NM_018179.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1270,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 8823,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000261168.9",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_018179.5",
          "protein_coding": true,
          "protein_id": "ENSP00000261168.4",
          "strand": true,
          "transcript": "ENST00000261168.9",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1278,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4847,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3837,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000544627.5",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2887-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000440440.1",
          "strand": true,
          "transcript": "ENST00000544627.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1270,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4142,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 14,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000540793.5",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 9,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000444589.1",
          "strand": true,
          "transcript": "ENST00000540793.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1269,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8774,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3810,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000536444.5",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2860-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000445955.1",
          "strand": true,
          "transcript": "ENST00000536444.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1105,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4887,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3318,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 13,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000543189.5",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2860-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000443179.1",
          "strand": true,
          "transcript": "ENST00000543189.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1278,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8797,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3837,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_181352.2",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2887-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_851997.1",
          "strand": true,
          "transcript": "NM_181352.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1277,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8794,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3834,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001388179.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2884-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001375108.1",
          "strand": true,
          "transcript": "NM_001388179.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1276,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4469,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3831,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000884191.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000554250.1",
          "strand": true,
          "transcript": "ENST00000884191.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1276,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4103,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3831,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000969302.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000639361.1",
          "strand": true,
          "transcript": "ENST00000969302.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 1270,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 9067,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
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          ],
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          "exon_rank": null,
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          "feature": "NM_001388180.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001375109.1",
          "strand": true,
          "transcript": "NM_001388180.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_length": 1270,
          "aa_ref": null,
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          "biotype": "protein_coding",
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          "cdna_end": null,
          "cdna_length": 8732,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
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          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001388181.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001375110.1",
          "strand": true,
          "transcript": "NM_001388181.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
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          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8779,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
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          "feature": "NM_001388182.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001375111.1",
          "strand": true,
          "transcript": "NM_001388182.1",
          "transcript_support_level": null
        },
        {
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          "cdna_length": 9286,
          "cdna_start": null,
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          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
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          "exon_rank_end": null,
          "feature": "NM_001388183.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001375112.1",
          "strand": true,
          "transcript": "NM_001388183.1",
          "transcript_support_level": null
        },
        {
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          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4159,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3813,
          "cds_start": null,
          "consequences": [
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          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000969304.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2863-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
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          "protein_coding": true,
          "protein_id": "ENSP00000639363.1",
          "strand": true,
          "transcript": "ENST00000969304.1",
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        },
        {
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          "aa_ref": null,
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          "cdna_length": 8820,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3810,
          "cds_start": null,
          "consequences": [
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          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001286514.2",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2860-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001273443.1",
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        },
        {
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          "cdna_start": null,
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          "consequences": [
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          ],
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          "exon_rank": null,
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          "feature": "NM_001388184.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
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          "intron_rank": 10,
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          "mane_plus": null,
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          "protein_coding": true,
          "protein_id": "NP_001375113.1",
          "strand": true,
          "transcript": "NM_001388184.1",
          "transcript_support_level": null
        },
        {
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          "aa_ref": null,
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          "cdna_length": 4324,
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          "cds_start": null,
          "consequences": [
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          ],
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          "feature": "ENST00000969301.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2860-755A>G",
          "hgvs_p": null,
          "intron_rank": 10,
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          "mane_plus": null,
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          "protein_coding": true,
          "protein_id": "ENSP00000639360.1",
          "strand": true,
          "transcript": "ENST00000969301.1",
          "transcript_support_level": null
        },
        {
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          "aa_length": 1248,
          "aa_ref": null,
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4128,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3747,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 14,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936267.1",
          "gene_hgnc_id": 20092,
          "gene_symbol": "ATF7IP",
          "hgvs_c": "c.2797-755A>G",
          "hgvs_p": null,
          "intron_rank": 9,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606326.1",
          "strand": true,
          "transcript": "ENST00000936267.1",
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        },
        {
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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.