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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: 7-134805711-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=134805711&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 134805711,
      "ref": "C",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000361675.7",
      "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "NM_033138.4",
          "protein_id": "NP_149129.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 793,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2382,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5011,
          "mane_select": "ENST00000361675.7",
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "ENST00000361675.7",
          "protein_id": "ENSP00000354826.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 793,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2382,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5011,
          "mane_select": "NM_033138.4",
          "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": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "ENST00000361901.6",
          "protein_id": "ENSP00000354513.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 538,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1617,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4114,
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "NM_001438765.1",
          "protein_id": "NP_001425694.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 792,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2379,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5008,
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "NM_001438767.1",
          "protein_id": "NP_001425696.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 574,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1725,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4110,
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-129-38173C>A",
          "hgvs_p": null,
          "transcript": "NM_001438769.1",
          "protein_id": "NP_001425698.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1695,
          "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": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-129-38173C>A",
          "hgvs_p": null,
          "transcript": "NM_001438770.1",
          "protein_id": "NP_001425699.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1695,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4404,
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "NM_001438771.1",
          "protein_id": "NP_001425700.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 564,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1695,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4324,
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "NM_033157.4",
          "protein_id": "NP_149347.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 563,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1692,
          "cdna_start": null,
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          "cdna_length": 4321,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
          "hgvs_p": null,
          "transcript": "ENST00000422748.5",
          "protein_id": "ENSP00000395710.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": 563,
          "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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          "canonical": false,
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          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-130+25962C>A",
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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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          "canonical": false,
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          "gene_symbol": "CALD1",
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        {
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        {
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          "gene_symbol": "CALD1",
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        {
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          "gene_symbol": "CALD1",
          "gene_hgnc_id": 1441,
          "hgvs_c": "c.-129-38173C>A",
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      "computational_source_selected": "BayesDel_noAF",
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      "acmg_by_gene": [
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          "verdict": "Likely_benign",
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          "verdict": "Likely_benign",
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          "inheritance_mode": "",
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        {
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          "verdict": "Likely_benign",
          "transcript": "XR_007060535.1",
          "gene_symbol": "LOC124901750",
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          "effects": [
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          "inheritance_mode": "",
          "hgvs_c": "n.29221+8953G>T",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  ],
  "message": null
}