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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: 13-35356607-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=35356607&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "13",
      "pos": 35356607,
      "ref": "T",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000379939.7",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": 38,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.6179+4284T>G",
          "hgvs_p": null,
          "transcript": "NM_001385012.1",
          "protein_id": "NP_001371941.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2967,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8904,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11200,
          "mane_select": "ENST00000379939.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": 38,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.6179+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000379939.7",
          "protein_id": "ENSP00000369271.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2967,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8904,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11200,
          "mane_select": "NM_001385012.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": 37,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.6170+4284T>G",
          "hgvs_p": null,
          "transcript": "NM_001379245.1",
          "protein_id": "NP_001366174.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2964,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8895,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11191,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": 38,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.6179+4284T>G",
          "hgvs_p": null,
          "transcript": "NM_015678.5",
          "protein_id": "NP_056493.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2946,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8841,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11137,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": 38,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.6179+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000400445.8",
          "protein_id": "ENSP00000383295.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2946,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8841,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.4025+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000688626.1",
          "protein_id": "ENSP00000509239.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2228,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6687,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8429,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.3929+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000688363.1",
          "protein_id": "ENSP00000510178.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2198,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8327,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.1823+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000629018.4",
          "protein_id": "ENSP00000486239.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1494,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4485,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5980,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "c.527-95485T>G",
          "hgvs_p": null,
          "transcript": "ENST00000686320.1",
          "protein_id": "ENSP00000508724.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1020,
          "cds_start": -4,
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          "cds_length": 3063,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
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          "exon_rank": null,
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          "exon_count": 34,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "NBEA",
          "gene_hgnc_id": 7648,
          "hgvs_c": "n.2097+4284T>G",
          "hgvs_p": null,
          "transcript": "ENST00000686386.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "mane_select": null,
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        {
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          "gene_symbol": "NBEA",
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        {
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          "intron_rank": 17,
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          "gene_symbol": "NBEA",
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      "gene_symbol": "NBEA",
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      "dbsnp": "rs1197850",
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      "gnomad_exomes_af": null,
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      "gnomad_genomes_homalt": 7097,
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      "computational_score_selected": -0.8999999761581421,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.9,
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      "phylop100way_score": 0.079,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
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      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
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            "BA1"
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          "verdict": "Benign",
          "transcript": "ENST00000379939.7",
          "gene_symbol": "NBEA",
          "hgnc_id": 7648,
          "effects": [
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          "inheritance_mode": "AD",
          "hgvs_c": "c.6179+4284T>G",
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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
}