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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: 4-99046632-T-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=99046632&ref=T&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 99046632,
      "ref": "T",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_015143.3",
      "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.787+1322T>A",
          "hgvs_p": null,
          "transcript": "NM_015143.3",
          "protein_id": "NP_055958.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 386,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1161,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000296411.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_015143.3"
        },
        {
          "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.787+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000296411.11",
          "protein_id": "ENSP00000296411.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 386,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1161,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_015143.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000296411.11"
        },
        {
          "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": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.121+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000514051.1",
          "protein_id": "ENSP00000422689.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 116,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 351,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000514051.1"
        },
        {
          "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.784+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000869926.1",
          "protein_id": "ENSP00000539985.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 385,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1158,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000869926.1"
        },
        {
          "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": 12,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.784+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000969299.1",
          "protein_id": "ENSP00000639358.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 385,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1158,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000969299.1"
        },
        {
          "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.787+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000924347.1",
          "protein_id": "ENSP00000594406.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000924347.1"
        },
        {
          "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.757+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000869927.1",
          "protein_id": "ENSP00000539986.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 376,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1131,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000869927.1"
        },
        {
          "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": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.730+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000869928.1",
          "protein_id": "ENSP00000539987.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 367,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1104,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000869928.1"
        },
        {
          "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": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.787+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000869925.1",
          "protein_id": "ENSP00000539984.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 364,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1095,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000869925.1"
        },
        {
          "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": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.730+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000924346.1",
          "protein_id": "ENSP00000594405.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 345,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1038,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000924346.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.787+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000924345.1",
          "protein_id": "ENSP00000594404.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 316,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 951,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000924345.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 8,
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          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.784+1322T>A",
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          "transcript": "ENST00000924348.1",
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          "aa_length": 315,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000924348.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.538+1322T>A",
          "hgvs_p": null,
          "transcript": "ENST00000969300.1",
          "protein_id": "ENSP00000639359.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cdna_start": null,
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        {
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          "canonical": false,
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          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.140-2101T>A",
          "hgvs_p": null,
          "transcript": "ENST00000510133.5",
          "protein_id": "ENSP00000423071.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 170,
          "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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          "gene_symbol": "METAP1",
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "exon_count": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.682+1322T>A",
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          "transcript": "XM_011531778.3",
          "protein_id": "XP_011530080.1",
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          "aa_length": 351,
          "cds_start": null,
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        {
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          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.656-2101T>A",
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          "transcript": "XM_011531779.3",
          "protein_id": "XP_011530081.1",
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          "cds_start": null,
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          "gene_symbol": "METAP1",
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        {
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          "gene_symbol": "METAP1",
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        {
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          ],
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          "exon_count": 12,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "METAP1",
          "gene_hgnc_id": 15789,
          "hgvs_c": "c.637+1322T>A",
          "hgvs_p": null,
          "transcript": "XM_047449884.1",
          "protein_id": "XP_047305840.1",
          "transcript_support_level": null,
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          "aa_length": 336,
          "cds_start": null,
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          "cds_length": 1011,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "XM_047449884.1"
        },
        {
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          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "verdict": "Likely_benign",
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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
}