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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: 20-25226018-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=25226018&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 25226018,
      "ref": "A",
      "alt": "G",
      "effect": "3_prime_UTR_variant",
      "transcript": "ENST00000376652.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001247.5",
          "protein_id": "NP_001238.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 484,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1455,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4104,
          "mane_select": "ENST00000376652.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "ENST00000376652.9",
          "protein_id": "ENSP00000365840.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 484,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1455,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4104,
          "mane_select": "NM_001247.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "ENST00000360031.6",
          "protein_id": "ENSP00000353131.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2766,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "ENST00000354989.10",
          "protein_id": "ENSP00000347084.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 456,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1371,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2708,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "n.1877A>G",
          "hgvs_p": null,
          "transcript": "ENST00000485936.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 2588,
          "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": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "n.1207A>G",
          "hgvs_p": null,
          "transcript": "ENST00000490187.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 1918,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001322378.2",
          "protein_id": "NP_001309307.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 484,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1455,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4230,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001317941.3",
          "protein_id": "NP_001304870.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4101,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001322398.2",
          "protein_id": "NP_001309327.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 481,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1446,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4161,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
          "hgvs_p": null,
          "transcript": "NM_001322397.2",
          "protein_id": "NP_001309326.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 471,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1416,
          "cdna_start": null,
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          "cdna_length": 4147,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
          "hgvs_p": null,
          "transcript": "NM_001322396.2",
          "protein_id": "NP_001309325.2",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 470,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": null,
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          "cdna_length": 4144,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
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          "transcript": "NM_001322395.2",
          "protein_id": "NP_001309324.2",
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          "aa_length": 468,
          "cds_start": -4,
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          "cdna_start": null,
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        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 14,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001114089.4",
          "protein_id": "NP_001107561.2",
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          "cds_start": -4,
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          "cdna_start": null,
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        {
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          "strand": true,
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          ],
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001322394.2",
          "protein_id": "NP_001309323.2",
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          "aa_length": 466,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "canonical": false,
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          "strand": true,
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            "3_prime_UTR_variant"
          ],
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
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        {
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          "consequences": [
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          ],
          "exon_rank": 14,
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          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
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          "transcript": "NM_001322392.2",
          "protein_id": "NP_001309321.2",
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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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          "feature": null
        },
        {
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 15,
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          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null,
          "transcript": "NM_001322390.2",
          "protein_id": "NP_001309319.2",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
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        {
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          ],
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*421A>G",
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          "transcript": "NM_001322389.2",
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        {
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          "consequences": [
            "3_prime_UTR_variant"
          ],
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ENTPD6",
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          "hgvs_c": "c.*503A>G",
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          "transcript": "NM_001322388.2",
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          "cdna_start": null,
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          "cdna_length": 4045,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENTPD6",
          "gene_hgnc_id": 3368,
          "hgvs_c": "c.*503A>G",
          "hgvs_p": null,
          "transcript": "ENST00000433259.6",
          "protein_id": "ENSP00000401895.2",
          "transcript_support_level": 5,
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          "cds_start": -4,
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      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.95,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.988,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "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": "ENST00000376652.9",
          "gene_symbol": "ENTPD6",
          "hgnc_id": 3368,
          "effects": [
            "3_prime_UTR_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.*421A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}