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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: 19-5928174-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=5928174&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 5928174,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_007322.3",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.694-87A>G",
          "hgvs_p": null,
          "transcript": "NM_007322.3",
          "protein_id": "NP_015561.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 567,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1704,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000340578.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_007322.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.694-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000340578.10",
          "protein_id": "ENSP00000341483.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 567,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1704,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_007322.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000340578.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.679-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000439268.6",
          "protein_id": "ENSP00000404837.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 562,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1689,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000439268.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000034275.12",
          "protein_id": "ENSP00000034275.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 499,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1500,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000034275.12"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.475-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000591092.5",
          "protein_id": "ENSP00000465085.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 494,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1485,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000591092.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "n.996-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000587411.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000587411.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "n.*405-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000592771.5",
          "protein_id": "ENSP00000466879.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000592771.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.679-87A>G",
          "hgvs_p": null,
          "transcript": "NM_003624.3",
          "protein_id": "NP_003615.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 562,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1689,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_003624.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-87A>G",
          "hgvs_p": null,
          "transcript": "NM_007320.3",
          "protein_id": "NP_015559.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 499,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1500,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_007320.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-90A>G",
          "hgvs_p": null,
          "transcript": "ENST00000852125.1",
          "protein_id": "ENSP00000522184.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852125.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000852119.1",
          "protein_id": "ENSP00000522178.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 497,
          "cds_start": null,
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          "cds_length": 1494,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.475-87A>G",
          "hgvs_p": null,
          "transcript": "NM_001300865.2",
          "protein_id": "NP_001287794.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": 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": 7,
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          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.475-87A>G",
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          "transcript": "ENST00000852122.1",
          "protein_id": "ENSP00000522181.1",
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          "aa_length": 492,
          "cds_start": null,
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          "cdna_start": null,
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        {
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          "strand": false,
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          ],
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          "exon_count": 15,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.424-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000852124.1",
          "protein_id": "ENSP00000522183.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 477,
          "cds_start": null,
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          "cdna_start": null,
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        {
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          "transcript": "ENST00000852126.1",
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        },
        {
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          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.382-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000852118.1",
          "protein_id": "ENSP00000522177.1",
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          "aa_start": null,
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        {
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          "exon_count": 15,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-2437A>G",
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          "transcript": "ENST00000852120.1",
          "protein_id": "ENSP00000522179.1",
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          "cds_start": null,
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        },
        {
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          "intron_rank": 7,
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          "gene_symbol": "RANBP3",
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        {
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          "canonical": false,
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          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.295-87A>G",
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          "transcript": "ENST00000852117.1",
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          "feature": "ENST00000852117.1"
        },
        {
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          ],
          "exon_rank": null,
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          "exon_count": 12,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "RANBP3",
          "gene_hgnc_id": 9850,
          "hgvs_c": "c.490-87A>G",
          "hgvs_p": null,
          "transcript": "ENST00000852123.1",
          "protein_id": "ENSP00000522182.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 367,
          "cds_start": null,
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          "cds_length": 1104,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852123.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 2,
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      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.20999999344348907,
      "splice_prediction_selected": "Uncertain_significance",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.89,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.682,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.21,
      "spliceai_max_prediction": "Uncertain_significance",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -8,
      "acmg_classification": "Benign",
      "acmg_criteria": "BA1",
      "acmg_by_gene": [
        {
          "score": -8,
          "benign_score": 8,
          "pathogenic_score": 0,
          "criteria": [
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_007322.3",
          "gene_symbol": "RANBP3",
          "hgnc_id": 9850,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.694-87A>G",
          "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
}