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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: 4-185691521-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=185691521&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 185691521,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_001395207.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null,
          "transcript": "NM_001395207.1",
          "protein_id": "NP_001382136.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1300,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000695409.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001395207.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null,
          "transcript": "ENST00000695409.1",
          "protein_id": "ENSP00000511888.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1300,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001395207.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000695409.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-197-12699C>G",
          "hgvs_p": null,
          "transcript": "ENST00000284776.11",
          "protein_id": "ENSP00000284776.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1100,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3303,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000284776.11"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-233-12699C>G",
          "hgvs_p": null,
          "transcript": "ENST00000437304.6",
          "protein_id": "ENSP00000396008.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 824,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2475,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000437304.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-32-6675C>G",
          "hgvs_p": null,
          "transcript": "ENST00000319471.13",
          "protein_id": "ENSP00000322182.9",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 731,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2196,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000319471.13"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null,
          "transcript": "ENST00000393528.7",
          "protein_id": "ENSP00000377162.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 666,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2001,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000393528.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-78-910C>G",
          "hgvs_p": null,
          "transcript": "ENST00000449407.6",
          "protein_id": "ENSP00000397262.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 644,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1935,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000449407.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null,
          "transcript": "ENST00000319454.10",
          "protein_id": "ENSP00000321983.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 635,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1909,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000319454.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "n.-197-12699C>G",
          "hgvs_p": null,
          "transcript": "ENST00000487184.2",
          "protein_id": "ENSP00000511890.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000487184.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null,
          "transcript": "ENST00000421420.6",
          "protein_id": "ENSP00000393258.2",
          "transcript_support_level": 4,
          "aa_start": null,
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          "aa_length": 1572,
          "cds_start": null,
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          "cds_length": 4719,
          "cdna_start": null,
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        {
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          "strand": false,
          "consequences": [
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          ],
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          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-32-6675C>G",
          "hgvs_p": null,
          "transcript": "NM_001394245.1",
          "protein_id": "NP_001381174.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1286,
          "cds_start": null,
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          "cds_length": 3861,
          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 2,
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          "gene_symbol": "SORBS2",
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          "cds_start": null,
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        {
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          "gene_symbol": "SORBS2",
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        {
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          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
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          "gene_symbol": "SORBS2",
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          "transcript": "NM_001394250.1",
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        {
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          "transcript": "NM_001270771.3",
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        {
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          "intron_rank": 1,
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          "gene_symbol": "SORBS2",
          "gene_hgnc_id": 24098,
          "hgvs_c": "c.-40-910C>G",
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          "transcript": "NM_001394253.1",
          "protein_id": "NP_001381182.1",
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        },
        {
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          ],
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          "gene_symbol": "SORBS2",
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          "hgvs_c": "n.318-12699C>G",
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          "transcript": "ENST00000698538.1",
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          "biotype": "retained_intron",
          "feature": "ENST00000698538.1"
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      ],
      "gene_symbol": "SORBS2",
      "gene_hgnc_id": 24098,
      "dbsnp": "rs4376189",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9300000071525574,
      "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": -0.93,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.718,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001395207.1",
          "gene_symbol": "SORBS2",
          "hgnc_id": 24098,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.-40-910C>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}