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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: 4-158680511-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=158680511&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 158680511,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000511912.6",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "NM_004453.4",
          "protein_id": "NP_004444.2",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 617,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1854,
          "cdna_start": 240,
          "cdna_end": null,
          "cdna_length": 3111,
          "mane_select": "ENST00000511912.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000511912.6",
          "protein_id": "ENSP00000426638.1",
          "transcript_support_level": 1,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 617,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1854,
          "cdna_start": 240,
          "cdna_end": null,
          "cdna_length": 3111,
          "mane_select": "NM_004453.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.86+8021C>A",
          "hgvs_p": null,
          "transcript": "ENST00000506422.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 865,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000684622.1",
          "protein_id": "ENSP00000507546.1",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 618,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1857,
          "cdna_start": 270,
          "cdna_end": null,
          "cdna_length": 2227,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000684505.1",
          "protein_id": "ENSP00000508237.1",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 600,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1803,
          "cdna_start": 240,
          "cdna_end": null,
          "cdna_length": 4155,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000682456.1",
          "protein_id": "ENSP00000508240.1",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 570,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1713,
          "cdna_start": 270,
          "cdna_end": null,
          "cdna_length": 4093,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000683483.1",
          "protein_id": "ENSP00000507719.1",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 569,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1710,
          "cdna_start": 270,
          "cdna_end": null,
          "cdna_length": 4090,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "c.79C>A",
          "hgvs_p": "p.Pro27Thr",
          "transcript": "ENST00000684641.1",
          "protein_id": "ENSP00000507642.1",
          "transcript_support_level": null,
          "aa_start": 27,
          "aa_end": null,
          "aa_length": 522,
          "cds_start": 79,
          "cds_end": null,
          "cds_length": 1569,
          "cdna_start": 270,
          "cdna_end": null,
          "cdna_length": 3949,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.330C>A",
          "hgvs_p": null,
          "transcript": "ENST00000436096.3",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1411,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.328C>A",
          "hgvs_p": null,
          "transcript": "ENST00000681978.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 5579,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.104C>A",
          "hgvs_p": null,
          "transcript": "ENST00000682178.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5077,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.188C>A",
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          "transcript": "ENST00000682409.1",
          "protein_id": null,
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        },
        {
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          "protein_coding": false,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.410C>A",
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        },
        {
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.270C>A",
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          "mane_select": null,
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        },
        {
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          "strand": true,
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ETFDH",
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          "hgvs_c": "n.116C>A",
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        {
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          ],
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.386C>A",
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          "transcript": "ENST00000682910.1",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.79C>A",
          "hgvs_p": null,
          "transcript": "ENST00000683004.1",
          "protein_id": "ENSP00000506936.1",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.79C>A",
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.79C>A",
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        {
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          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.79C>A",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ETFDH",
          "gene_hgnc_id": 3483,
          "hgvs_c": "n.202C>A",
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          "transcript": "ENST00000683750.1",
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}