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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: 5-102831450-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=102831450&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 102831450,
      "ref": "C",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000438793.8",
      "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": 26,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "NM_001177306.2",
          "protein_id": "NP_001170777.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 973,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2922,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3990,
          "mane_select": "ENST00000438793.8",
          "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": 26,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "ENST00000438793.8",
          "protein_id": "ENSP00000396493.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 973,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2922,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3990,
          "mane_select": "NM_001177306.2",
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "ENST00000304400.12",
          "protein_id": "ENSP00000306100.8",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 973,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2922,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3832,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "ENST00000455264.7",
          "protein_id": "ENSP00000403461.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 905,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2718,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3430,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "ENST00000348126.7",
          "protein_id": "ENSP00000314638.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3649,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "NM_001319943.1",
          "protein_id": "NP_001306872.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 991,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2976,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5955,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "NM_000919.4",
          "protein_id": "NP_000910.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 974,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2925,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3993,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "ENST00000684529.1",
          "protein_id": "ENSP00000507038.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 974,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2925,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3993,
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "NM_001364583.2",
          "protein_id": "NP_001351512.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 973,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5379,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 26,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "NM_001364584.2",
          "protein_id": "NP_001351513.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 972,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": false,
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          "intron_rank": 1,
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          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-374+23219C>A",
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          "transcript_support_level": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": false,
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          "gene_symbol": "PAM",
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          "hgvs_c": "c.-374+23219C>A",
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          "gene_symbol": "PAM",
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          "hgvs_p": null,
          "transcript": "XM_047417254.1",
          "protein_id": "XP_047273210.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
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          "cdna_length": 5279,
          "mane_select": null,
          "mane_plus": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 1,
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          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "XM_047417255.1",
          "protein_id": "XP_047273211.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
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          "cdna_length": 5276,
          "mane_select": null,
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          "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": 22,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PAM",
          "gene_hgnc_id": 8596,
          "hgvs_c": "c.-373-34373C>A",
          "hgvs_p": null,
          "transcript": "XM_047417256.1",
          "protein_id": "XP_047273212.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 694,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2085,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5222,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PAM",
      "gene_hgnc_id": 8596,
      "dbsnp": "rs467693",
      "frequency_reference_population": 0.000013447367,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.0000134474,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8500000238418579,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.85,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.123,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "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": "ENST00000438793.8",
          "gene_symbol": "PAM",
          "hgnc_id": 8596,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.-373-34373C>A",
          "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
}