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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: 11-7628409-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=7628409&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 7628409,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000299492.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "NM_003621.5",
          "protein_id": "NP_003612.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3328,
          "mane_select": "ENST00000299492.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "ENST00000299492.9",
          "protein_id": "ENSP00000299492.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3328,
          "mane_select": "NM_003621.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.414+63C>T",
          "hgvs_p": null,
          "transcript": "ENST00000533792.5",
          "protein_id": "ENSP00000436498.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 718,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2157,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3003,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351853.2",
          "protein_id": "NP_001338782.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 928,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2787,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3060,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "ENST00000684123.1",
          "protein_id": "ENSP00000507842.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 927,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2784,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3274,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351854.2",
          "protein_id": "NP_001338783.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 917,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2754,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3027,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351855.2",
          "protein_id": "NP_001338784.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 887,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2664,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3361,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.894+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351856.2",
          "protein_id": "NP_001338785.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3334,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.888+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351862.2",
          "protein_id": "NP_001338791.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": -4,
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          "cds_length": 2631,
          "cdna_start": null,
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          "cdna_length": 3484,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "c.657+63C>T",
          "hgvs_p": null,
          "transcript": "NM_001351857.2",
          "protein_id": "NP_001338786.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 850,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2553,
          "cdna_start": null,
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          "cdna_length": 4447,
          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "canonical": false,
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          "consequences": [
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          "exon_rank": null,
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          "exon_count": 23,
          "intron_rank": 7,
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          "gene_symbol": "PPFIBP2",
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          "hgvs_c": "c.657+63C>T",
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          "transcript": "NM_001351858.2",
          "protein_id": "NP_001338787.2",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": 2523,
          "cdna_start": null,
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          "cdna_length": 3188,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
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        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
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          "hgvs_c": "c.657+63C>T",
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        {
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          "intron_rank": 7,
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          "gene_symbol": "PPFIBP2",
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          "hgvs_c": "c.657+63C>T",
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          "gene_symbol": "PPFIBP2",
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          "transcript": "NM_001351860.2",
          "protein_id": "NP_001338789.2",
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        {
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          "gene_symbol": "PPFIBP2",
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          "transcript": "NM_001256568.2",
          "protein_id": "NP_001243497.2",
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        {
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          "intron_rank": 6,
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          "gene_symbol": "PPFIBP2",
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          "transcript": "ENST00000528883.5",
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        {
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        {
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          "gene_symbol": "PPFIBP2",
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          "transcript": "ENST00000529575.5",
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          "cdna_start": null,
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          "cdna_length": 780,
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          "feature": null
        },
        {
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          "strand": true,
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          ],
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          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PPFIBP2",
          "gene_hgnc_id": 9250,
          "hgvs_c": "n.317-27005C>T",
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      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6600000262260437,
      "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": -0.66,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.352,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000299492.9",
          "gene_symbol": "PPFIBP2",
          "hgnc_id": 9250,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.888+63C>T",
          "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
}