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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: 4-152411746-T-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=152411746&ref=T&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 152411746,
      "ref": "T",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000281708.10",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "NM_001349798.2",
          "protein_id": "NP_001336727.1",
          "transcript_support_level": null,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1236,
          "cdna_end": null,
          "cdna_length": 5639,
          "mane_select": "ENST00000281708.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000281708.10",
          "protein_id": "ENSP00000281708.3",
          "transcript_support_level": 1,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1236,
          "cdna_end": null,
          "cdna_length": 5639,
          "mane_select": "NM_001349798.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000603548.6",
          "protein_id": "ENSP00000474725.1",
          "transcript_support_level": 1,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1250,
          "cdna_end": null,
          "cdna_length": 5653,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000603841.1",
          "protein_id": "ENSP00000474971.1",
          "transcript_support_level": 1,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 133,
          "cdna_end": null,
          "cdna_length": 2261,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000604872.6",
          "protein_id": "ENSP00000474751.1",
          "transcript_support_level": 1,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 176,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 531,
          "cdna_start": 335,
          "cdna_end": null,
          "cdna_length": 921,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "NM_033632.3",
          "protein_id": "NP_361014.1",
          "transcript_support_level": null,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 220,
          "cdna_end": null,
          "cdna_length": 3909,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000703553.1",
          "protein_id": "ENSP00000515369.1",
          "transcript_support_level": null,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 689,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 2070,
          "cdna_start": 743,
          "cdna_end": null,
          "cdna_length": 2755,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "NM_001257069.1",
          "protein_id": "NP_001243998.1",
          "transcript_support_level": null,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 176,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 531,
          "cdna_start": 385,
          "cdna_end": null,
          "cdna_length": 971,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000605042.1",
          "protein_id": "ENSP00000474538.1",
          "transcript_support_level": 3,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 157,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 475,
          "cdna_start": 254,
          "cdna_end": null,
          "cdna_length": 671,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000642901.1",
          "protein_id": "ENSP00000495905.1",
          "transcript_support_level": null,
          "aa_start": 20,
          "aa_end": null,
          "aa_length": 69,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 211,
          "cdna_start": 242,
          "cdna_end": null,
          "cdna_length": 395,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000643834.1",
          "protein_id": "ENSP00000495702.1",
          "transcript_support_level": null,
          "aa_start": 20,
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          "aa_length": 69,
          "cds_start": 58,
          "cds_end": null,
          "cds_length": 211,
          "cdna_start": 292,
          "cdna_end": null,
          "cdna_length": 445,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "ENST00000647166.1",
          "protein_id": "ENSP00000495753.1",
          "transcript_support_level": null,
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          "cds_start": 58,
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          "cdna_start": 502,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "XM_011532084.3",
          "protein_id": "XP_011530386.1",
          "transcript_support_level": null,
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          "cds_start": 58,
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          "cdna_start": 1186,
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          "mane_select": null,
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "XM_011532085.3",
          "protein_id": "XP_011530387.1",
          "transcript_support_level": null,
          "aa_start": 20,
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          "cdna_start": 1093,
          "cdna_end": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          ],
          "exon_rank": 5,
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          "intron_rank": null,
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          "gene_symbol": "FBXW7",
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          "hgvs_c": "c.58A>T",
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          "transcript": "XM_024454123.2",
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        {
          "aa_ref": "R",
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          ],
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          "exon_count": 17,
          "intron_rank": null,
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          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "XM_047415897.1",
          "protein_id": "XP_047271853.1",
          "transcript_support_level": null,
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          "cdna_start": 42610,
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        {
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          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
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          "cdna_start": 574,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "R",
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          "strand": false,
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          ],
          "exon_rank": 3,
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          "gene_symbol": "FBXW7",
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          "hgvs_c": "c.58A>T",
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
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          "biotype": null,
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        },
        {
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          "protein_coding": true,
          "strand": false,
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          ],
          "exon_rank": 4,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "c.58A>T",
          "hgvs_p": "p.Arg20*",
          "transcript": "XM_047415901.1",
          "protein_id": "XP_047271857.1",
          "transcript_support_level": null,
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          "cds_start": 58,
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          "cdna_start": 7584,
          "cdna_end": null,
          "cdna_length": 11987,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FBXW7",
          "gene_hgnc_id": 16712,
          "hgvs_c": "n.58A>T",
          "hgvs_p": null,
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
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      "custom_annotations": null
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  "message": null
}