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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: 17-68522748-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=68522748&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 68522748,
      "ref": "T",
      "alt": "G",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "ENST00000589228.6",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_002734.5",
          "protein_id": "NP_002725.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4253,
          "mane_select": "ENST00000589228.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "ENST00000589228.6",
          "protein_id": "ENSP00000464977.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4253,
          "mane_select": "NM_002734.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "ENST00000358598.6",
          "protein_id": "ENSP00000351410.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3576,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "ENST00000536854.6",
          "protein_id": "ENSP00000445625.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3697,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "ENST00000586397.5",
          "protein_id": "ENSP00000466459.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1940,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_001276289.2",
          "protein_id": "NP_001263218.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4386,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_001278433.2",
          "protein_id": "NP_001265362.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4307,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_001369389.1",
          "protein_id": "NP_001356318.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4410,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_001369390.1",
          "protein_id": "NP_001356319.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": null,
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          "cdna_length": 4221,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_212471.3",
          "protein_id": "NP_997636.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
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        {
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          "canonical": false,
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          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "NM_212472.2",
          "protein_id": "NP_997637.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 381,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": null
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        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "intron_rank": 2,
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          "gene_symbol": "PRKAR1A",
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          "cds_start": -4,
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        {
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          "gene_symbol": "PRKAR1A",
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          "transcript": "ENST00000585427.6",
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        {
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          ],
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          "intron_rank": 2,
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          "gene_symbol": "PRKAR1A",
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          "hgvs_c": "c.178-8T>G",
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          "transcript": "ENST00000588178.6",
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        {
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          ],
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          "exon_count": 12,
          "intron_rank": 3,
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          "gene_symbol": "PRKAR1A",
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          ],
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          "intron_rank": 2,
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          "gene_symbol": "PRKAR1A",
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          "hgvs_c": "c.178-8T>G",
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          "transcript": "ENST00000592800.6",
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          "transcript": "ENST00000585981.6",
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKAR1A",
          "gene_hgnc_id": 9388,
          "hgvs_c": "c.178-8T>G",
          "hgvs_p": null,
          "transcript": "ENST00000588188.7",
          "protein_id": "ENSP00000468106.2",
          "transcript_support_level": 3,
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          "cds_start": -4,
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        {
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      "gene_symbol": "PRKAR1A",
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      "dbsnp": "rs771192586",
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      "gnomad_exomes_homalt": 0,
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      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": -0.4699999988079071,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.3059999942779541,
      "splice_prediction_selected": "Benign",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.47,
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      "phylop100way_score": 1.233,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.0218837639555862,
      "dbscsnv_ada_prediction": "Benign",
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      "mitotip_score": null,
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      "acmg_score": -17,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2_Supporting",
      "acmg_by_gene": [
        {
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          "benign_score": 17,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS1",
            "BS2_Supporting"
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          "verdict": "Benign",
          "transcript": "ENST00000589228.6",
          "gene_symbol": "PRKAR1A",
          "hgnc_id": 9388,
          "effects": [
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            "intron_variant"
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          "inheritance_mode": "AD",
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        {
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          "pathogenic_score": 2,
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            "BP4_Strong",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000590353.1",
          "gene_symbol": "ENSG00000267009",
          "hgnc_id": null,
          "effects": [
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            "intron_variant"
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          "inheritance_mode": "",
          "hgvs_c": "n.357-8T>G",
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      ],
      "clinvar_disease": " type 1,Carney complex,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "Carney complex, type 1|not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}