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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: 10-3144385-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=3144385&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 3144385,
      "ref": "A",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_001242307.2",
      "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": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2458-19T>A",
          "hgvs_p": null,
          "transcript": "NM_014889.4",
          "protein_id": "NP_055704.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000224949.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_014889.4"
        },
        {
          "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": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2458-19T>A",
          "hgvs_p": null,
          "transcript": "ENST00000224949.9",
          "protein_id": "ENSP00000224949.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_014889.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000224949.9"
        },
        {
          "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": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2461-19T>A",
          "hgvs_p": null,
          "transcript": "ENST00000380989.6",
          "protein_id": "ENSP00000370377.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000380989.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1-AS1",
          "gene_hgnc_id": 44675,
          "hgvs_c": "n.346+399A>T",
          "hgvs_p": null,
          "transcript": "ENST00000430356.3",
          "protein_id": null,
          "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": "pseudogene",
          "feature": "ENST00000430356.3"
        },
        {
          "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": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "n.2051-19T>A",
          "hgvs_p": null,
          "transcript": "ENST00000464395.1",
          "protein_id": null,
          "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": "retained_intron",
          "feature": "ENST00000464395.1"
        },
        {
          "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": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2461-19T>A",
          "hgvs_p": null,
          "transcript": "NM_001242307.2",
          "protein_id": "NP_001229236.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1038,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3117,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242307.2"
        },
        {
          "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": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2446-19T>A",
          "hgvs_p": null,
          "transcript": "ENST00000851395.1",
          "protein_id": "ENSP00000521454.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1033,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3102,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000851395.1"
        },
        {
          "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": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2443-19T>A",
          "hgvs_p": null,
          "transcript": "ENST00000960314.1",
          "protein_id": "ENSP00000630373.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000960314.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2434-19T>A",
          "hgvs_p": null,
          "transcript": "NM_001347729.1",
          "protein_id": "NP_001334658.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1029,
          "cds_start": null,
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          "cds_length": 3090,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001347729.1"
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 21,
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          "gene_symbol": "PITRM1",
          "gene_hgnc_id": 17663,
          "hgvs_c": "c.2413-19T>A",
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          "transcript": "ENST00000960311.1",
          "protein_id": "ENSP00000630370.1",
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          "cds_start": null,
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        {
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          "transcript": "ENST00000678987.1",
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          "cdna_start": null,
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          "gene_symbol": "PITRM1",
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          "gene_symbol": "PITRM1",
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          "transcript": "ENST00000451104.6",
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      "gnomad_exomes_af": 0.0000305423,
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      "gnomad_genomes_ac": 4,
      "gnomad_exomes_homalt": 0,
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      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": -0.8700000047683716,
      "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,
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      "bayesdelnoaf_score": -0.87,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.069,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "mitotip_score": null,
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      "acmg_score": -6,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate",
      "acmg_by_gene": [
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          "benign_score": 6,
          "pathogenic_score": 0,
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            "BP6_Moderate"
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          "verdict": "Likely_benign",
          "transcript": "NM_001242307.2",
          "gene_symbol": "PITRM1",
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        {
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            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000430356.3",
          "gene_symbol": "PITRM1-AS1",
          "hgnc_id": 44675,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.346+399A>T",
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        {
          "score": -6,
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          "pathogenic_score": 0,
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            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000441377.2",
          "gene_symbol": "ENSG00000278419",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.251+399A>T",
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}