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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: 7-128990049-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=128990049&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "7",
      "pos": 128990049,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000265388.10",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1410G>A",
          "hgvs_p": "p.Pro470Pro",
          "transcript": "NM_012470.4",
          "protein_id": "NP_036602.1",
          "transcript_support_level": null,
          "aa_start": 470,
          "aa_end": null,
          "aa_length": 923,
          "cds_start": 1410,
          "cds_end": null,
          "cds_length": 2772,
          "cdna_start": 1751,
          "cdna_end": null,
          "cdna_length": 4345,
          "mane_select": "ENST00000265388.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1410G>A",
          "hgvs_p": "p.Pro470Pro",
          "transcript": "ENST00000265388.10",
          "protein_id": "ENSP00000265388.5",
          "transcript_support_level": 1,
          "aa_start": 470,
          "aa_end": null,
          "aa_length": 923,
          "cds_start": 1410,
          "cds_end": null,
          "cds_length": 2772,
          "cdna_start": 1751,
          "cdna_end": null,
          "cdna_length": 4345,
          "mane_select": "NM_012470.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1410G>A",
          "hgvs_p": "p.Pro470Pro",
          "transcript": "ENST00000471234.5",
          "protein_id": "ENSP00000418646.1",
          "transcript_support_level": 1,
          "aa_start": 470,
          "aa_end": null,
          "aa_length": 859,
          "cds_start": 1410,
          "cds_end": null,
          "cds_length": 2580,
          "cdna_start": 1784,
          "cdna_end": null,
          "cdna_length": 3283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1212G>A",
          "hgvs_p": "p.Pro404Pro",
          "transcript": "ENST00000482320.5",
          "protein_id": "ENSP00000420089.1",
          "transcript_support_level": 1,
          "aa_start": 404,
          "aa_end": null,
          "aa_length": 857,
          "cds_start": 1212,
          "cds_end": null,
          "cds_length": 2574,
          "cdna_start": 1894,
          "cdna_end": null,
          "cdna_length": 3585,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1512G>A",
          "hgvs_p": "p.Pro504Pro",
          "transcript": "NM_001382216.1",
          "protein_id": "NP_001369145.1",
          "transcript_support_level": null,
          "aa_start": 504,
          "aa_end": null,
          "aa_length": 957,
          "cds_start": 1512,
          "cds_end": null,
          "cds_length": 2874,
          "cdna_start": 1853,
          "cdna_end": null,
          "cdna_length": 4447,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1512G>A",
          "hgvs_p": "p.Pro504Pro",
          "transcript": "ENST00000471166.1",
          "protein_id": "ENSP00000418267.1",
          "transcript_support_level": 5,
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          "cds_start": 1512,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1512G>A",
          "hgvs_p": "p.Pro504Pro",
          "transcript": "ENST00000627585.2",
          "protein_id": "ENSP00000487231.1",
          "transcript_support_level": 2,
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          "aa_end": null,
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          "cds_start": 1512,
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          "cds_length": 2874,
          "cdna_start": 1915,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "TNPO3",
          "gene_hgnc_id": 17103,
          "hgvs_c": "c.1491G>A",
          "hgvs_p": "p.Pro497Pro",
          "transcript": "NM_001382217.1",
          "protein_id": "NP_001369146.1",
          "transcript_support_level": null,
          "aa_start": 497,
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          "aa_length": 950,
          "cds_start": 1491,
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          "cdna_start": 1832,
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        {
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          "intron_rank": null,
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          "gene_symbol": "TNPO3",
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        {
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          "consequences": [
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        {
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        {
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          ],
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        {
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          "consequences": [
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          ],
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "TNPO3",
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        {
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "TNPO3",
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      "computational_score_selected": -0.27000001072883606,
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      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
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      "bayesdelnoaf_score": -0.27,
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      "phylop100way_score": -0.691,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
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      "acmg_score": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Moderate,BP7,BS2",
      "acmg_by_gene": [
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          "verdict": "Benign",
          "transcript": "ENST00000265388.10",
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      "clinvar_disease": "Autosomal dominant limb-girdle muscular dystrophy type 1F",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Autosomal dominant limb-girdle muscular dystrophy type 1F",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}