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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: 11-14890871-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=14890871&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 14890871,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000334636.10",
      "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": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.225+1110A>G",
          "hgvs_p": null,
          "transcript": "NM_024514.5",
          "protein_id": "NP_078790.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 501,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1506,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2214,
          "mane_select": "ENST00000334636.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.225+1110A>G",
          "hgvs_p": null,
          "transcript": "ENST00000334636.10",
          "protein_id": "ENSP00000334592.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 501,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1506,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2214,
          "mane_select": "NM_024514.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "n.-66+282A>G",
          "hgvs_p": null,
          "transcript": "ENST00000530609.5",
          "protein_id": "ENSP00000466060.1",
          "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": 1882,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "n.-66+282A>G",
          "hgvs_p": null,
          "transcript": "ENST00000534686.5",
          "protein_id": "ENSP00000432087.2",
          "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": 1668,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "n.801A>G",
          "hgvs_p": null,
          "transcript": "NR_174512.1",
          "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,
          "cdna_end": null,
          "cdna_length": 2055,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "n.801A>G",
          "hgvs_p": null,
          "transcript": "NR_174514.1",
          "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,
          "cdna_end": null,
          "cdna_length": 2279,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "n.801A>G",
          "hgvs_p": null,
          "transcript": "NR_174515.1",
          "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,
          "cdna_end": null,
          "cdna_length": 2688,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-281A>G",
          "hgvs_p": null,
          "transcript": "NM_001377215.1",
          "protein_id": "NP_001364144.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 386,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1161,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-481A>G",
          "hgvs_p": null,
          "transcript": "NM_001400560.1",
          "protein_id": "NP_001387489.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 386,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1161,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3124,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-226A>G",
          "hgvs_p": null,
          "transcript": "NM_001400563.1",
          "protein_id": "NP_001387492.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 268,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 807,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2515,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-2013A>G",
          "hgvs_p": null,
          "transcript": "XM_047426360.1",
          "protein_id": "XP_047282316.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 446,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1341,
          "cdna_start": null,
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          "cdna_length": 4836,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-2013A>G",
          "hgvs_p": null,
          "transcript": "XM_047426363.1",
          "protein_id": "XP_047282319.1",
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          "aa_start": null,
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          "aa_length": 288,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "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": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "PDE3B",
          "gene_hgnc_id": 8779,
          "hgvs_c": "c.2887-8085T>C",
          "hgvs_p": null,
          "transcript": "NM_001429699.1",
          "protein_id": "NP_001416628.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1016,
          "cds_start": -4,
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          "cds_length": 3051,
          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "PDE3B",
          "gene_hgnc_id": 8779,
          "hgvs_c": "c.2887-8074T>C",
          "hgvs_p": null,
          "transcript": "NM_001429700.1",
          "protein_id": "NP_001416629.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 982,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2949,
          "cdna_start": null,
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          "cdna_length": 3535,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.180+493A>G",
          "hgvs_p": null,
          "transcript": "NM_001400568.1",
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.43+282A>G",
          "hgvs_p": null,
          "transcript": "NM_001400567.1",
          "protein_id": "NP_001387496.1",
          "transcript_support_level": null,
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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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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.25+29A>G",
          "hgvs_p": null,
          "transcript": "NM_001377217.1",
          "protein_id": "NP_001364146.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-121+29A>G",
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          "transcript": "NM_001377214.1",
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        },
        {
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          "intron_rank": 1,
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          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-121+82A>G",
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          "transcript": "NM_001377216.1",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 1,
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          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-121+282A>G",
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          "transcript": "NM_001377227.1",
          "protein_id": "NP_001364156.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2482,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "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": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.-121+1494A>G",
          "hgvs_p": null,
          "transcript": "NM_001400558.1",
          "protein_id": "NP_001387487.1",
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          "cdna_end": null,
          "cdna_length": 4432,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CYP2R1",
          "gene_hgnc_id": 20580,
          "hgvs_c": "c.225+1110A>G",
          "hgvs_p": null,
          "transcript": "XM_047426362.1",
          "protein_id": "XP_047282318.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 343,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1032,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1120,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CYP2R1",
      "gene_hgnc_id": 20580,
      "dbsnp": "rs7129781",
      "frequency_reference_population": 0.08360943,
      "hom_count_reference_population": 3872,
      "allele_count_reference_population": 82369,
      "gnomad_exomes_af": 0.0801562,
      "gnomad_genomes_af": 0.102526,
      "gnomad_exomes_ac": 66777,
      "gnomad_genomes_ac": 15592,
      "gnomad_exomes_homalt": 2831,
      "gnomad_genomes_homalt": 1041,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8700000047683716,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.87,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.338,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000334636.10",
          "gene_symbol": "CYP2R1",
          "hgnc_id": 20580,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.225+1110A>G",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_001429699.1",
          "gene_symbol": "PDE3B",
          "hgnc_id": 8779,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2887-8085T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": " chronic obstructive, susceptibility to,Pulmonary disease",
      "clinvar_classification": "association",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Pulmonary disease, chronic obstructive, susceptibility to",
      "pathogenicity_classification_combined": "association",
      "custom_annotations": null
    }
  ],
  "message": null
}