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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: 8-143917605-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143917605&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 143917605,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000345136.8",
      "consequences": [
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12216C>T",
          "hgvs_p": "p.Phe4072Phe",
          "transcript": "NM_201384.3",
          "protein_id": "NP_958786.1",
          "transcript_support_level": null,
          "aa_start": 4072,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 12216,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": 12352,
          "cdna_end": null,
          "cdna_length": 14804,
          "mane_select": "ENST00000345136.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12216C>T",
          "hgvs_p": "p.Phe4072Phe",
          "transcript": "ENST00000345136.8",
          "protein_id": "ENSP00000344848.3",
          "transcript_support_level": 1,
          "aa_start": 4072,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 12216,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": 12352,
          "cdna_end": null,
          "cdna_length": 14804,
          "mane_select": "NM_201384.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12174C>T",
          "hgvs_p": "p.Phe4058Phe",
          "transcript": "NM_201378.4",
          "protein_id": "NP_958780.1",
          "transcript_support_level": null,
          "aa_start": 4058,
          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 12174,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": 12231,
          "cdna_end": null,
          "cdna_length": 14683,
          "mane_select": null,
          "mane_plus": "ENST00000356346.7",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12174C>T",
          "hgvs_p": "p.Phe4058Phe",
          "transcript": "ENST00000356346.7",
          "protein_id": "ENSP00000348702.3",
          "transcript_support_level": 1,
          "aa_start": 4058,
          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 12174,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": 12231,
          "cdna_end": null,
          "cdna_length": 14683,
          "mane_select": null,
          "mane_plus": "NM_201378.4",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12627C>T",
          "hgvs_p": "p.Phe4209Phe",
          "transcript": "ENST00000322810.8",
          "protein_id": "ENSP00000323856.4",
          "transcript_support_level": 1,
          "aa_start": 4209,
          "aa_end": null,
          "aa_length": 4684,
          "cds_start": 12627,
          "cds_end": null,
          "cds_length": 14055,
          "cdna_start": 12797,
          "cdna_end": null,
          "cdna_length": 15249,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12297C>T",
          "hgvs_p": "p.Phe4099Phe",
          "transcript": "ENST00000436759.6",
          "protein_id": "ENSP00000388180.2",
          "transcript_support_level": 1,
          "aa_start": 4099,
          "aa_end": null,
          "aa_length": 4574,
          "cds_start": 12297,
          "cds_end": null,
          "cds_length": 13725,
          "cdna_start": 12335,
          "cdna_end": null,
          "cdna_length": 14787,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12228C>T",
          "hgvs_p": "p.Phe4076Phe",
          "transcript": "ENST00000357649.6",
          "protein_id": "ENSP00000350277.2",
          "transcript_support_level": 1,
          "aa_start": 4076,
          "aa_end": null,
          "aa_length": 4551,
          "cds_start": 12228,
          "cds_end": null,
          "cds_length": 13656,
          "cdna_start": 12237,
          "cdna_end": null,
          "cdna_length": 14689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12216C>T",
          "hgvs_p": "p.Phe4072Phe",
          "transcript": "ENST00000354589.7",
          "protein_id": "ENSP00000346602.3",
          "transcript_support_level": 1,
          "aa_start": 4072,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 12216,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": 12284,
          "cdna_end": null,
          "cdna_length": 14736,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12150C>T",
          "hgvs_p": "p.Phe4050Phe",
          "transcript": "ENST00000354958.6",
          "protein_id": "ENSP00000347044.2",
          "transcript_support_level": 1,
          "aa_start": 4050,
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          "aa_length": 4525,
          "cds_start": 12150,
          "cds_end": null,
          "cds_length": 13578,
          "cdna_start": 12299,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12120C>T",
          "hgvs_p": "p.Phe4040Phe",
          "transcript": "ENST00000398774.6",
          "protein_id": "ENSP00000381756.2",
          "transcript_support_level": 1,
          "aa_start": 4040,
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          "cds_start": 12120,
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        },
        {
          "aa_ref": "F",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_count": 32,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12627C>T",
          "hgvs_p": "p.Phe4209Phe",
          "transcript": "NM_201380.4",
          "protein_id": "NP_958782.1",
          "transcript_support_level": null,
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          "cds_start": 12627,
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        },
        {
          "aa_ref": "F",
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          "exon_count": 34,
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          "gene_symbol": "PLEC",
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          "hgvs_c": "c.12348C>T",
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          "transcript": "ENST00000528025.6",
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          "cds_start": 12348,
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        {
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          "strand": false,
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          "intron_rank": null,
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          "gene_symbol": "PLEC",
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          "hgvs_c": "c.12297C>T",
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          "protein_id": "NP_000436.2",
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        {
          "aa_ref": "F",
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          "protein_coding": true,
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          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12285C>T",
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          "transcript": "ENST00000527096.5",
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        {
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        {
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          "strand": false,
          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12228C>T",
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          "transcript": "NM_201383.3",
          "protein_id": "NP_958785.1",
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        {
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          "transcript": "NM_201382.4",
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        {
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.12120C>T",
          "hgvs_p": "p.Phe4040Phe",
          "transcript": "NM_201381.3",
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        },
        {
          "aa_ref": "F",
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          "strand": false,
          "consequences": [
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          ],
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      "computational_source_selected": "BayesDel_noAF",
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      "acmg_classification": "Benign",
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      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:2 B:1",
      "phenotype_combined": "not provided|Autosomal recessive limb-girdle muscular dystrophy type 2Q;Epidermolysis bullosa simplex, Ogna type;Epidermolysis bullosa simplex 5B, with muscular dystrophy;Epidermolysis bullosa simplex with nail dystrophy;Epidermolysis bullosa simplex 5C, with pyloric atresia|PLEC-related disorder",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
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  "message": null
}