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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: 1-34988717-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=34988717&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 11,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BP7",
            "BS2"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "ZMYM6",
          "hgnc_id": 13050,
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "inheritance_mode": "AD",
          "pathogenic_score": 0,
          "score": -11,
          "transcript": "NM_007167.4",
          "verdict": "Benign"
        },
        {
          "benign_score": 6,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "ENSG00000271741",
          "hgnc_id": null,
          "hgvs_c": "n.2146+3517T>C",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 2,
          "score": -4,
          "transcript": "ENST00000487874.1",
          "verdict": "Likely_benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BP7,BS2",
      "acmg_score": -11,
      "allele_count_reference_population": 44,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "G",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.6,
      "chr": "1",
      "clinvar_classification": "Likely benign",
      "clinvar_disease": "not provided",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.6000000238418579,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5122,
          "cdna_start": 2570,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": 16,
          "exon_rank_end": null,
          "feature": "NM_007167.4",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000357182.9",
          "protein_coding": true,
          "protein_id": "NP_009098.3",
          "strand": false,
          "transcript": "NM_007167.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5122,
          "cdna_start": 2570,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": 16,
          "exon_rank_end": null,
          "feature": "ENST00000357182.9",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_007167.4",
          "protein_coding": true,
          "protein_id": "ENSP00000349708.4",
          "strand": false,
          "transcript": "ENST00000357182.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6241,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 15,
          "exon_rank": 15,
          "exon_rank_end": null,
          "feature": "ENST00000493328.5",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "n.3689T>C",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000493328.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 3099,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000487874.1",
          "gene_hgnc_id": null,
          "gene_symbol": "ENSG00000271741",
          "hgvs_c": "n.2146+3517T>C",
          "hgvs_p": null,
          "intron_rank": 15,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000421752.1",
          "strand": false,
          "transcript": "ENST00000487874.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1349,
          "aa_ref": "L",
          "aa_start": 813,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4351,
          "cdna_start": 2614,
          "cds_end": null,
          "cds_length": 4050,
          "cds_start": 2437,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 17,
          "exon_rank_end": null,
          "feature": "ENST00000859306.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2437T>C",
          "hgvs_p": "p.Leu813Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000529365.1",
          "strand": false,
          "transcript": "ENST00000859306.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5124,
          "cdna_start": 2551,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": 16,
          "exon_rank_end": null,
          "feature": "ENST00000859303.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000529362.1",
          "strand": false,
          "transcript": "ENST00000859303.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4364,
          "cdna_start": 2630,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 17,
          "exon_rank_end": null,
          "feature": "ENST00000929017.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000599076.1",
          "strand": false,
          "transcript": "ENST00000929017.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4343,
          "cdna_start": 2608,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 17,
          "exon_rank_end": null,
          "feature": "ENST00000929018.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000599077.1",
          "strand": false,
          "transcript": "ENST00000929018.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6008,
          "cdna_start": 3459,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": 15,
          "exon_rank_end": null,
          "feature": "ENST00000965365.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635424.1",
          "strand": false,
          "transcript": "ENST00000965365.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4191,
          "cdna_start": 2455,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": 16,
          "exon_rank_end": null,
          "feature": "ENST00000965366.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635425.1",
          "strand": false,
          "transcript": "ENST00000965366.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1325,
          "aa_ref": "L",
          "aa_start": 789,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4360,
          "cdna_start": 2624,
          "cds_end": null,
          "cds_length": 3978,
          "cds_start": 2365,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 17,
          "exon_rank_end": null,
          "feature": "ENST00000965367.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2365T>C",
          "hgvs_p": "p.Leu789Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635426.1",
          "strand": false,
          "transcript": "ENST00000965367.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1280,
          "aa_ref": "L",
          "aa_start": 744,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4964,
          "cdna_start": 2417,
          "cds_end": null,
          "cds_length": 3843,
          "cds_start": 2230,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": 16,
          "exon_rank_end": null,
          "feature": "ENST00000859302.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2230T>C",
          "hgvs_p": "p.Leu744Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000529361.1",
          "strand": false,
          "transcript": "ENST00000859302.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1232,
          "aa_ref": "L",
          "aa_start": 696,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4033,
          "cdna_start": 2297,
          "cds_end": null,
          "cds_length": 3699,
          "cds_start": 2086,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": 15,
          "exon_rank_end": null,
          "feature": "ENST00000929016.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2086T>C",
          "hgvs_p": "p.Leu696Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000599075.1",
          "strand": false,
          "transcript": "ENST00000929016.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 864,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3711,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2595,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 16,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000859304.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2147-1165T>C",
          "hgvs_p": null,
          "intron_rank": 15,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000529363.1",
          "strand": false,
          "transcript": "ENST00000859304.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 864,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2899,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2595,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 16,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000859305.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2147-1165T>C",
          "hgvs_p": null,
          "intron_rank": 15,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000529364.1",
          "strand": false,
          "transcript": "ENST00000859305.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 864,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4125,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2595,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000929015.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.2147-1165T>C",
          "hgvs_p": null,
          "intron_rank": 14,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000599074.1",
          "strand": false,
          "transcript": "ENST00000929015.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 800,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2663,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2403,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000965368.1",
          "gene_hgnc_id": 13050,
          "gene_symbol": "ZMYM6",
          "hgvs_c": "c.1955-1165T>C",
          "hgvs_p": null,
          "intron_rank": 14,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635427.1",
          "strand": false,
          "transcript": "ENST00000965368.1",
          "transcript_support_level": null
        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
      "dbscsnv_ada_score": null,
      "dbsnp": "rs1021275304",
      "effect": "synonymous_variant",
      "frequency_reference_population": 0.000028365064,
      "gene_hgnc_id": 13050,
      "gene_symbol": "ZMYM6",
      "gnomad_exomes_ac": 39,
      "gnomad_exomes_af": 0.0000278778,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_ac": 5,
      "gnomad_genomes_af": 0.0000328429,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_heteroplasmic": null,
      "gnomad_mito_homoplasmic": null,
      "hom_count_reference_population": 0,
      "mitotip_prediction": null,
      "mitotip_score": null,
      "pathogenicity_classification_combined": "Likely benign",
      "phenotype_combined": "not provided",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": 1.538,
      "pos": 34988717,
      "ref": "A",
      "revel_prediction": null,
      "revel_score": null,
      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0,
      "transcript": "NM_007167.4"
    }
  ]
}
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