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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: 11-126407321-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=126407321&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 126407321,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000444328.7",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr",
          "transcript": "NM_001254757.2",
          "protein_id": "NP_001241686.1",
          "transcript_support_level": null,
          "aa_start": 84,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": 252,
          "cds_end": null,
          "cds_length": 1002,
          "cdna_start": 469,
          "cdna_end": null,
          "cdna_length": 1810,
          "mane_select": "ENST00000444328.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr",
          "transcript": "ENST00000444328.7",
          "protein_id": "ENSP00000394354.2",
          "transcript_support_level": 5,
          "aa_start": 84,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": 252,
          "cds_end": null,
          "cds_length": 1002,
          "cdna_start": 469,
          "cdna_end": null,
          "cdna_length": 1810,
          "mane_select": "NM_001254757.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr",
          "transcript": "ENST00000392669.6",
          "protein_id": "ENSP00000376437.2",
          "transcript_support_level": 1,
          "aa_start": 84,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": 252,
          "cds_end": null,
          "cds_length": 1002,
          "cdna_start": 383,
          "cdna_end": null,
          "cdna_length": 1724,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr",
          "transcript": "ENST00000526727.5",
          "protein_id": "ENSP00000436047.1",
          "transcript_support_level": 1,
          "aa_start": 84,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": 252,
          "cds_end": null,
          "cds_length": 1002,
          "cdna_start": 626,
          "cdna_end": null,
          "cdna_length": 1967,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.249C>T",
          "hgvs_p": "p.Tyr83Tyr",
          "transcript": "ENST00000532243.5",
          "protein_id": "ENSP00000434349.1",
          "transcript_support_level": 1,
          "aa_start": 83,
          "aa_end": null,
          "aa_length": 332,
          "cds_start": 249,
          "cds_end": null,
          "cds_length": 999,
          "cdna_start": 514,
          "cdna_end": null,
          "cdna_length": 1825,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.240C>T",
          "hgvs_p": "p.Tyr80Tyr",
          "transcript": "ENST00000530591.5",
          "protein_id": "ENSP00000433989.1",
          "transcript_support_level": 1,
          "aa_start": 80,
          "aa_end": null,
          "aa_length": 329,
          "cds_start": 240,
          "cds_end": null,
          "cds_length": 990,
          "cdna_start": 709,
          "cdna_end": null,
          "cdna_length": 1459,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.237C>T",
          "hgvs_p": "p.Tyr79Tyr",
          "transcript": "ENST00000534457.5",
          "protein_id": "ENSP00000434668.1",
          "transcript_support_level": 1,
          "aa_start": 79,
          "aa_end": null,
          "aa_length": 328,
          "cds_start": 237,
          "cds_end": null,
          "cds_length": 987,
          "cdna_start": 237,
          "cdna_end": null,
          "cdna_length": 987,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.-241C>T",
          "hgvs_p": null,
          "transcript": "ENST00000524860.1",
          "protein_id": "ENSP00000431170.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 152,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 460,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1012,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.315C>T",
          "hgvs_p": "p.Tyr105Tyr",
          "transcript": "NM_001348396.2",
          "protein_id": "NP_001335325.1",
          "transcript_support_level": null,
          "aa_start": 105,
          "aa_end": null,
          "aa_length": 354,
          "cds_start": 315,
          "cds_end": null,
          "cds_length": 1065,
          "cdna_start": 620,
          "cdna_end": null,
          "cdna_length": 1961,
          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.315C>T",
          "hgvs_p": "p.Tyr105Tyr",
          "transcript": "NM_001348397.2",
          "protein_id": "NP_001335326.1",
          "transcript_support_level": null,
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          "cdna_start": 754,
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        {
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          "hgvs_c": "c.315C>T",
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          "transcript": "ENST00000356132.9",
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        {
          "aa_ref": "Y",
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          "consequences": [
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        {
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          "gene_symbol": "ST3GAL4",
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          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr",
          "transcript": "NM_001348399.2",
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        {
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        {
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          "strand": true,
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          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.240C>T",
          "hgvs_p": "p.Tyr80Tyr",
          "transcript": "NM_006278.3",
          "protein_id": "NP_006269.1",
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          "cds_start": 240,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "gene_symbol": "ST3GAL4",
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        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "n.469C>T",
          "hgvs_p": null,
          "transcript": "NR_145671.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1985,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL4",
          "gene_hgnc_id": 10864,
          "hgvs_c": "c.-241C>T",
          "hgvs_p": null,
          "transcript": "ENST00000524860.1",
          "protein_id": "ENSP00000431170.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 152,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 460,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1012,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ST3GAL4",
      "gene_hgnc_id": 10864,
      "dbsnp": "rs2230278",
      "frequency_reference_population": 0.31064025,
      "hom_count_reference_population": 79495,
      "allele_count_reference_population": 501287,
      "gnomad_exomes_af": 0.310087,
      "gnomad_genomes_af": 0.315958,
      "gnomad_exomes_ac": 453233,
      "gnomad_genomes_ac": 48054,
      "gnomad_exomes_homalt": 71688,
      "gnomad_genomes_homalt": 7807,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6800000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.68,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -3.062,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000444328.7",
          "gene_symbol": "ST3GAL4",
          "hgnc_id": 10864,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.252C>T",
          "hgvs_p": "p.Tyr84Tyr"
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}