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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: 14-20454990-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=20454990&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 20454990,
      "ref": "T",
      "alt": "C",
      "effect": "non_coding_transcript_exon_variant",
      "transcript": "ENST00000556439.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSGEP",
          "gene_hgnc_id": 18028,
          "hgvs_c": "n.64A>G",
          "hgvs_p": null,
          "transcript": "ENST00000556252.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 830,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSGEP",
          "gene_hgnc_id": 18028,
          "hgvs_c": "n.100A>G",
          "hgvs_p": null,
          "transcript": "ENST00000556439.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1011,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSGEP",
          "gene_hgnc_id": 18028,
          "hgvs_c": "c.-307A>G",
          "hgvs_p": null,
          "transcript": "NM_017807.4",
          "protein_id": "NP_060277.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 335,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1008,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1976,
          "mane_select": "ENST00000206542.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSGEP",
          "gene_hgnc_id": 18028,
          "hgvs_c": "c.-307A>G",
          "hgvs_p": null,
          "transcript": "ENST00000206542.9",
          "protein_id": "ENSP00000206542.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 335,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1008,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1976,
          "mane_select": "NM_017807.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-473T>C",
          "hgvs_p": null,
          "transcript": "NM_001641.4",
          "protein_id": "NP_001632.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 957,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1453,
          "mane_select": "ENST00000216714.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-473T>C",
          "hgvs_p": null,
          "transcript": "ENST00000216714.8",
          "protein_id": "ENSP00000216714.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 957,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1453,
          "mane_select": "NM_001641.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-407T>C",
          "hgvs_p": null,
          "transcript": "ENST00000398030.8",
          "protein_id": "ENSP00000381111.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 957,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1387,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-417T>C",
          "hgvs_p": null,
          "transcript": "ENST00000555414.5",
          "protein_id": "ENSP00000451979.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 957,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "n.-236T>C",
          "hgvs_p": null,
          "transcript": "ENST00000553555.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1603,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-468T>C",
          "hgvs_p": null,
          "transcript": "NM_001244249.2",
          "protein_id": "NP_001231178.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 957,
          "cdna_start": null,
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          "cdna_length": 1448,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-407T>C",
          "hgvs_p": null,
          "transcript": "NM_080648.3",
          "protein_id": "NP_542379.1",
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          "aa_start": null,
          "aa_end": null,
          "aa_length": 318,
          "cds_start": -4,
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          "cds_length": 957,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-417T>C",
          "hgvs_p": null,
          "transcript": "NM_080649.3",
          "protein_id": "NP_542380.1",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": null,
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          "intron_rank": null,
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          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-319T>C",
          "hgvs_p": null,
          "transcript": "ENST00000553681.5",
          "protein_id": "ENSP00000451327.1",
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          "cds_start": -4,
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        {
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          "gene_symbol": "APEX1",
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          "hgvs_c": "c.-473T>C",
          "hgvs_p": null,
          "transcript": "ENST00000555839.5",
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "OSGEP",
          "gene_hgnc_id": 18028,
          "hgvs_c": "c.-307A>G",
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          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-468T>C",
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          "transcript": "ENST00000557344.5",
          "protein_id": "ENSP00000452137.1",
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          "cdna_length": 671,
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "c.-480T>C",
          "hgvs_p": null,
          "transcript": "ENST00000557181.5",
          "protein_id": "ENSP00000452304.1",
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        {
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": null,
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          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "n.-473T>C",
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          "gene_symbol": "OSGEP",
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          "hgvs_c": "n.-197A>G",
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          ],
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          "gene_symbol": "APEX1",
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          "hgvs_c": "n.-225T>C",
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          "transcript": "ENST00000554813.5",
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": null,
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          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "n.-236T>C",
          "hgvs_p": null,
          "transcript": "ENST00000555306.5",
          "protein_id": null,
          "transcript_support_level": 5,
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "n.-229T>C",
          "hgvs_p": null,
          "transcript": "ENST00000556296.1",
          "protein_id": null,
          "transcript_support_level": 4,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 571,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "APEX1",
          "gene_hgnc_id": 587,
          "hgvs_c": "n.-250T>C",
          "hgvs_p": null,
          "transcript": "ENST00000557159.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1803,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "OSGEP",
      "gene_hgnc_id": 18028,
      "dbsnp": "rs1760944",
      "frequency_reference_population": 0.000006577822,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 0,
      "gnomad_genomes_af": 0.00000657782,
      "gnomad_exomes_ac": 0,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7900000214576721,
      "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": -0.79,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.119,
      "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": "ENST00000556439.1",
          "gene_symbol": "OSGEP",
          "hgnc_id": 18028,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "n.100A>G",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000216714.8",
          "gene_symbol": "APEX1",
          "hgnc_id": 587,
          "effects": [
            "upstream_gene_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.-473T>C",
          "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
}