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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: 19-14149034-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=14149034&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 14149034,
      "ref": "G",
      "alt": "A",
      "effect": "3_prime_UTR_variant",
      "transcript": "ENST00000361434.8",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "NM_014921.5",
          "protein_id": "NP_055736.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1469,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4410,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7820,
          "mane_select": "ENST00000361434.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "ENST00000361434.8",
          "protein_id": "ENSP00000355328.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1469,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4410,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7820,
          "mane_select": "NM_014921.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "ENST00000340736.10",
          "protein_id": "ENSP00000340688.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1474,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4425,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7853,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1-AS1",
          "gene_hgnc_id": 55309,
          "hgvs_c": "n.80-6118G>A",
          "hgvs_p": null,
          "transcript": "ENST00000588387.3",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": 2895,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "NM_001008701.3",
          "protein_id": "NP_001008701.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1474,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4425,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7835,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "XM_017026475.2",
          "protein_id": "XP_016881964.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1506,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4521,
          "cdna_start": null,
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          "cdna_length": 7931,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "XM_017026476.2",
          "protein_id": "XP_016881965.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1506,
          "cds_start": -4,
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          "cds_length": 4521,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8041,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
          "hgvs_c": "c.*1839C>T",
          "hgvs_p": null,
          "transcript": "XM_024451420.2",
          "protein_id": "XP_024307188.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1506,
          "cds_start": -4,
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          "cds_length": 4521,
          "cdna_start": null,
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          "cdna_length": 8984,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "ADGRL1",
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          "hgvs_c": "c.*1839C>T",
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          "transcript": "XM_047438413.1",
          "protein_id": "XP_047294369.1",
          "transcript_support_level": null,
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          "mane_select": null,
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        {
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "ADGRL1",
          "gene_hgnc_id": 20973,
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          "protein_id": "XP_011526098.1",
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          "intron_rank": null,
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      ],
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      "gnomad_exomes_af": 0.1175,
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      "computational_score_selected": -0.8600000143051147,
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      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.86,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.738,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
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      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
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          "benign_score": 12,
          "pathogenic_score": 0,
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          "verdict": "Benign",
          "transcript": "ENST00000361434.8",
          "gene_symbol": "ADGRL1",
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        {
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          "verdict": "Benign",
          "transcript": "ENST00000588387.3",
          "gene_symbol": "ADGRL1-AS1",
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          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.80-6118G>A",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}