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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: 19-51869723-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=51869723&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 51869723,
      "ref": "C",
      "alt": "T",
      "effect": "3_prime_UTR_variant",
      "transcript": "ENST00000638348.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_001370449.1",
          "protein_id": "NP_001357378.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8291,
          "mane_select": "ENST00000638348.2",
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "ENST00000638348.2",
          "protein_id": "ENSP00000491936.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8291,
          "mane_select": "NM_001370449.1",
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "ENST00000301399.12",
          "protein_id": "ENSP00000301399.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7308,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_001370447.1",
          "protein_id": "NP_001357376.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7360,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_001370448.1",
          "protein_id": "NP_001357377.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7372,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_032679.3",
          "protein_id": "NP_116068.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7308,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_001135590.2",
          "protein_id": "NP_001129062.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1281,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7195,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "NM_001370450.1",
          "protein_id": "NP_001357379.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1281,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8114,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "ENST00000451628.9",
          "protein_id": "ENSP00000389652.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1281,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7180,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "ENST00000639636.2",
          "protein_id": "ENSP00000491349.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1281,
          "cdna_start": null,
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          "cdna_length": 8099,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "XM_047439550.1",
          "protein_id": "XP_047295506.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 485,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 8965,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null,
          "transcript": "XM_047439551.1",
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.283+7559G>A",
          "hgvs_p": null,
          "transcript": "NM_001370452.1",
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          "transcript_support_level": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        },
        {
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          "intron_rank": 5,
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          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.283+7559G>A",
          "hgvs_p": null,
          "transcript": "NM_001370455.1",
          "protein_id": "NP_001357384.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 3693,
          "mane_select": null,
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        },
        {
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          ],
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          "gene_symbol": "ZNF577",
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        {
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          "intron_rank": 6,
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          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "c.283+7559G>A",
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          "transcript": "NM_001370457.1",
          "protein_id": "NP_001357386.1",
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          "cds_length": 327,
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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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          "strand": false,
          "consequences": [
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          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 5,
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          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "n.283+7559G>A",
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          "transcript": "ENST00000638827.1",
          "protein_id": "ENSP00000492704.1",
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          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "n.220+1905G>A",
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        {
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          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "n.400+7559G>A",
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        {
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          "consequences": [
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          ],
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          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "n.1561+7559G>A",
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          "cdna_length": 1800,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "ZNF577",
          "gene_hgnc_id": 28673,
          "hgvs_c": "n.1632+7559G>A",
          "hgvs_p": null,
          "transcript": "ENST00000640955.1",
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        {
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      ],
      "gene_symbol": "ZNF577",
      "gene_hgnc_id": 28673,
      "dbsnp": "rs10411161",
      "frequency_reference_population": 0.20692398,
      "hom_count_reference_population": 3923,
      "allele_count_reference_population": 31481,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.206924,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 31481,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 3923,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9200000166893005,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
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      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.92,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.681,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "mitotip_score": null,
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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"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000638348.2",
          "gene_symbol": "ZNF577",
          "hgnc_id": 28673,
          "effects": [
            "3_prime_UTR_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.*2809G>A",
          "hgvs_p": null
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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
}