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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: X-31203964-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=31203964&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 31203964,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000357033.9",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9804A>G",
          "hgvs_p": "p.Gln3268Gln",
          "transcript": "NM_004006.3",
          "protein_id": "NP_003997.2",
          "transcript_support_level": null,
          "aa_start": 3268,
          "aa_end": null,
          "aa_length": 3685,
          "cds_start": 9804,
          "cds_end": null,
          "cds_length": 11058,
          "cdna_start": 10041,
          "cdna_end": null,
          "cdna_length": 13992,
          "mane_select": "ENST00000357033.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9804A>G",
          "hgvs_p": "p.Gln3268Gln",
          "transcript": "ENST00000357033.9",
          "protein_id": "ENSP00000354923.3",
          "transcript_support_level": 1,
          "aa_start": 3268,
          "aa_end": null,
          "aa_length": 3685,
          "cds_start": 9804,
          "cds_end": null,
          "cds_length": 11058,
          "cdna_start": 10041,
          "cdna_end": null,
          "cdna_length": 13992,
          "mane_select": "NM_004006.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.600A>G",
          "hgvs_p": "p.Gln200Gln",
          "transcript": "ENST00000378723.7",
          "protein_id": "ENSP00000367997.3",
          "transcript_support_level": 1,
          "aa_start": 200,
          "aa_end": null,
          "aa_length": 635,
          "cds_start": 600,
          "cds_end": null,
          "cds_length": 1908,
          "cdna_start": 723,
          "cdna_end": null,
          "cdna_length": 4645,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.600A>G",
          "hgvs_p": "p.Gln200Gln",
          "transcript": "ENST00000361471.8",
          "protein_id": "ENSP00000354464.4",
          "transcript_support_level": 1,
          "aa_start": 200,
          "aa_end": null,
          "aa_length": 622,
          "cds_start": 600,
          "cds_end": null,
          "cds_length": 1869,
          "cdna_start": 678,
          "cdna_end": null,
          "cdna_length": 2224,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.600A>G",
          "hgvs_p": "p.Gln200Gln",
          "transcript": "ENST00000378702.8",
          "protein_id": "ENSP00000367974.4",
          "transcript_support_level": 1,
          "aa_start": 200,
          "aa_end": null,
          "aa_length": 617,
          "cds_start": 600,
          "cds_end": null,
          "cds_length": 1854,
          "cdna_start": 628,
          "cdna_end": null,
          "cdna_length": 2617,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.600A>G",
          "hgvs_p": "p.Gln200Gln",
          "transcript": "ENST00000378680.6",
          "protein_id": "ENSP00000367951.2",
          "transcript_support_level": 1,
          "aa_start": 200,
          "aa_end": null,
          "aa_length": 525,
          "cds_start": 600,
          "cds_end": null,
          "cds_length": 1578,
          "cdna_start": 720,
          "cdna_end": null,
          "cdna_length": 1858,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9792A>G",
          "hgvs_p": "p.Gln3264Gln",
          "transcript": "NM_004009.3",
          "protein_id": "NP_004000.1",
          "transcript_support_level": null,
          "aa_start": 3264,
          "aa_end": null,
          "aa_length": 3681,
          "cds_start": 9792,
          "cds_end": null,
          "cds_length": 11046,
          "cdna_start": 10055,
          "cdna_end": null,
          "cdna_length": 14000,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9792A>G",
          "hgvs_p": "p.Gln3264Gln",
          "transcript": "ENST00000378677.6",
          "protein_id": "ENSP00000367948.2",
          "transcript_support_level": 5,
          "aa_start": 3264,
          "aa_end": null,
          "aa_length": 3681,
          "cds_start": 9792,
          "cds_end": null,
          "cds_length": 11046,
          "cdna_start": 9987,
          "cdna_end": null,
          "cdna_length": 13932,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9780A>G",
          "hgvs_p": "p.Gln3260Gln",
          "transcript": "NM_000109.4",
          "protein_id": "NP_000100.3",
          "transcript_support_level": null,
          "aa_start": 3260,
          "aa_end": null,
          "aa_length": 3677,
          "cds_start": 9780,
          "cds_end": null,
          "cds_length": 11034,
          "cdna_start": 9903,
          "cdna_end": null,
          "cdna_length": 13854,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 67,
          "exon_rank_end": null,
          "exon_count": 79,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.9435A>G",
          "hgvs_p": "p.Gln3145Gln",
          "transcript": "NM_004010.3",
          "protein_id": "NP_004001.1",
          "transcript_support_level": null,
          "aa_start": 3145,
          "aa_end": null,
          "aa_length": 3562,
          "cds_start": 9435,
          "cds_end": null,
          "cds_length": 10689,
          "cdna_start": 10138,
          "cdna_end": null,
          "cdna_length": 14083,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.5781A>G",
          "hgvs_p": "p.Gln1927Gln",
          "transcript": "NM_004011.4",
          "protein_id": "NP_004002.3",
          "transcript_support_level": null,
          "aa_start": 1927,
          "aa_end": null,
          "aa_length": 2344,
          "cds_start": 5781,
          "cds_end": null,
          "cds_length": 7035,
          "cdna_start": 5800,
          "cdna_end": null,
          "cdna_length": 9751,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.5772A>G",
          "hgvs_p": "p.Gln1924Gln",
          "transcript": "NM_004012.4",
          "protein_id": "NP_004003.2",
          "transcript_support_level": null,
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          "cds_start": 5772,
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          "cds_length": 7026,
          "cdna_start": 5943,
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          "mane_select": null,
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        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 39,
          "exon_rank_end": null,
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          "intron_rank": null,
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.5772A>G",
          "hgvs_p": "p.Gln1924Gln",
          "transcript": "ENST00000619831.5",
          "protein_id": "ENSP00000479270.2",
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          "aa_length": 2341,
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        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 31,
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          "intron_rank": null,
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.4650A>G",
          "hgvs_p": "p.Gln1550Gln",
          "transcript": "ENST00000358062.7",
          "protein_id": "ENSP00000350765.3",
          "transcript_support_level": 5,
          "aa_start": 1550,
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          "cdna_start": 4650,
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        },
        {
          "aa_ref": "Q",
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          "gene_symbol": "DMD",
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          "hgvs_c": "c.2424A>G",
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        {
          "aa_ref": "Q",
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          "strand": false,
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          ],
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          "intron_rank": null,
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.2424A>G",
          "hgvs_p": "p.Gln808Gln",
          "transcript": "ENST00000474231.5",
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        {
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          "canonical": false,
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          "strand": false,
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          "intron_rank": null,
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          "gene_symbol": "DMD",
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          "hgvs_c": "c.2424A>G",
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          "transcript": "NM_004022.3",
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        {
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          "gene_symbol": "DMD",
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        {
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        {
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          "gene_symbol": "DMD",
          "gene_hgnc_id": 2928,
          "hgvs_c": "c.2424A>G",
          "hgvs_p": "p.Gln808Gln",
          "transcript": "ENST00000378707.7",
          "protein_id": "ENSP00000367979.3",
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          "cdna_start": 3465,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
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          "exon_count": 35,
          "intron_rank": null,
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      "computational_prediction_selected": "Uncertain_significance",
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      "bayesdelnoaf_score": -0.53,
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      "phylop100way_score": 0.2,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.37,
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      "acmg_score": -16,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP6_Very_Strong,BS1,BS2",
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      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:1 B:3",
      "phenotype_combined": "not specified|Cardiovascular phenotype|Duchenne muscular dystrophy|Becker muscular dystrophy;Cardiomyopathy;Duchenne muscular dystrophy;Dystrophin deficiency|not provided",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}