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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: 7-33177539-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=33177539&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 33177539,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000242067.11",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "NM_198428.3",
          "protein_id": "NP_940820.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 887,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2664,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 3996,
          "mane_select": "ENST00000242067.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "ENST00000242067.11",
          "protein_id": "ENSP00000242067.6",
          "transcript_support_level": 1,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 887,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2664,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 3996,
          "mane_select": "NM_198428.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.255T>C",
          "hgvs_p": "p.Asn85Asn",
          "transcript": "ENST00000425508.6",
          "protein_id": "ENSP00000405151.2",
          "transcript_support_level": 1,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 310,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 933,
          "cdna_start": 314,
          "cdna_end": null,
          "cdna_length": 1252,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "n.390T>C",
          "hgvs_p": null,
          "transcript": "ENST00000433714.5",
          "protein_id": "ENSP00000412159.1",
          "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": 3705,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.513T>C",
          "hgvs_p": "p.Asn171Asn",
          "transcript": "ENST00000671871.1",
          "protein_id": "ENSP00000499908.1",
          "transcript_support_level": null,
          "aa_start": 171,
          "aa_end": null,
          "aa_length": 928,
          "cds_start": 513,
          "cds_end": null,
          "cds_length": 2787,
          "cdna_start": 1016,
          "cdna_end": null,
          "cdna_length": 3822,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "NM_001348041.4",
          "protein_id": "NP_001334970.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 3712,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "ENST00000673056.1",
          "protein_id": "ENSP00000499989.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": 623,
          "cdna_end": null,
          "cdna_length": 3456,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "NM_001348036.1",
          "protein_id": "NP_001334965.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 887,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2664,
          "cdna_start": 669,
          "cdna_end": null,
          "cdna_length": 3785,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "NM_001348043.3",
          "protein_id": "NP_001334972.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 886,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2661,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 3993,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "NM_001033605.2",
          "protein_id": "NP_001028777.1",
          "transcript_support_level": null,
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          "aa_length": 882,
          "cds_start": 390,
          "cds_end": null,
          "cds_length": 2649,
          "cdna_start": 879,
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          "cdna_length": 3981,
          "mane_select": null,
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        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_rank": 5,
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "ENST00000355070.6",
          "protein_id": "ENSP00000347182.2",
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          "aa_length": 882,
          "cds_start": 390,
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          "cdna_start": 903,
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          "cdna_length": 4004,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
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          "intron_rank": null,
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          "gene_symbol": "BBS9",
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          "hgvs_c": "c.390T>C",
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          "transcript": "NM_001362679.1",
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          "cdna_start": 903,
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        {
          "aa_ref": "N",
          "aa_alt": "N",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "hgvs_c": "c.390T>C",
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        },
        {
          "aa_ref": "N",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "gene_symbol": "BBS9",
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          "hgvs_c": "c.390T>C",
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          "transcript": "NM_001033604.2",
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        {
          "aa_ref": "N",
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        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn",
          "transcript": "ENST00000672717.1",
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        {
          "aa_ref": "N",
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          "gene_symbol": "BBS9",
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          "transcript": "NM_014451.4",
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        {
          "aa_ref": "N",
          "aa_alt": "N",
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        },
        {
          "aa_ref": "N",
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          "gene_symbol": "BBS9",
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        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "BBS9",
          "gene_hgnc_id": 30000,
          "hgvs_c": "c.255T>C",
          "hgvs_p": "p.Asn85Asn",
          "transcript": "NM_001348042.3",
          "protein_id": "NP_001334971.1",
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          "cds_start": 255,
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          "cdna_length": 3873,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BBS9",
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      "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": -17,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1",
      "acmg_by_gene": [
        {
          "score": -17,
          "benign_score": 17,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000242067.11",
          "gene_symbol": "BBS9",
          "hgnc_id": 30000,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.390T>C",
          "hgvs_p": "p.Asn130Asn"
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000410809.1",
          "gene_symbol": "RNA5SP229",
          "hgnc_id": 43129,
          "effects": [
            "upstream_gene_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-201T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Bardet-Biedl syndrome,Bardet-Biedl syndrome 9,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:1 B:2",
      "phenotype_combined": "Bardet-Biedl syndrome|not specified|Bardet-Biedl syndrome 9",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}