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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: 12-124006982-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=124006982&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 124006982,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_152437.3",
      "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "NM_152437.3",
          "protein_id": "NP_689650.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000337815.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_152437.3"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000337815.9",
          "protein_id": "ENSP00000337320.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_152437.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000337815.9"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000392404.7",
          "protein_id": "ENSP00000376205.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000392404.7"
        },
        {
          "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": 6,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-661+2047G>C",
          "hgvs_p": null,
          "transcript": "ENST00000539644.5",
          "protein_id": "ENSP00000441405.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000539644.5"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "NM_001204298.2",
          "protein_id": "NP_001191227.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001204298.2"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000538932.6",
          "protein_id": "ENSP00000440645.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000538932.6"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000901659.1",
          "protein_id": "ENSP00000571718.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000901659.1"
        },
        {
          "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": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000901660.1",
          "protein_id": "ENSP00000571719.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000901660.1"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000901661.1",
          "protein_id": "ENSP00000571720.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000901661.1"
        },
        {
          "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": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null,
          "transcript": "ENST00000901662.1",
          "protein_id": "ENSP00000571721.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
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          "cds_length": 786,
          "cdna_start": null,
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          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-661+2047G>C",
          "hgvs_p": null,
          "transcript": "ENST00000901663.1",
          "protein_id": "ENSP00000571722.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 261,
          "cds_start": null,
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          "cds_length": 786,
          "cdna_start": null,
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          "mane_select": null,
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          "feature": "ENST00000901663.1"
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        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
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          "exon_rank": null,
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          "exon_count": 6,
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          "gene_symbol": "ZNF664",
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          "cds_start": null,
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        {
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          "gene_symbol": "ZNF664",
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        {
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          "exon_count": 6,
          "intron_rank": 4,
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          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-661+2047G>C",
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          "transcript": "ENST00000901666.1",
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        {
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        {
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          "intron_rank": 4,
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          "gene_symbol": "ZNF664",
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          "transcript": "ENST00000901668.1",
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          "gene_symbol": "ZNF664",
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          "hgvs_c": "c.-660-4399G>C",
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        {
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          ],
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          "intron_rank_end": null,
          "gene_symbol": "ZNF664",
          "gene_hgnc_id": 25406,
          "hgvs_c": "c.-661+2047G>C",
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          "transcript": "ENST00000901672.1",
          "protein_id": "ENSP00000571731.1",
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.91,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.264,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_152437.3",
          "gene_symbol": "ZNF664",
          "hgnc_id": 25406,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.-660-4399G>C",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_001204299.3",
          "gene_symbol": "ZNF664-RFLNA",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.-234+32962G>C",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000545615.1",
          "gene_symbol": "RFLNA",
          "hgnc_id": 27051,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "n.194+32962G>C",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000618862.2",
          "gene_symbol": "ENSG00000274874",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.369+18844G>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}