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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: 7-124859029-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=124859029&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 13,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "POT1",
          "hgnc_id": 17284,
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "inheritance_mode": "AR,AD",
          "pathogenic_score": 2,
          "score": -11,
          "transcript": "NM_015450.3",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Very_Strong,BP7",
      "acmg_score": -11,
      "allele_count_reference_population": 3,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.68,
      "chr": "7",
      "clinvar_classification": "Likely benign",
      "clinvar_disease": "Hereditary cancer-predisposing syndrome,Tumor predisposition syndrome 3",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.6800000071525574,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3924,
          "cdna_start": 1073,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "NM_015450.3",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000357628.8",
          "protein_coding": true,
          "protein_id": "NP_056265.2",
          "strand": false,
          "transcript": "NM_015450.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 3924,
          "cdna_start": 1073,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000357628.8",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_015450.3",
          "protein_coding": true,
          "protein_id": "ENSP00000350249.3",
          "strand": false,
          "transcript": "ENST00000357628.8",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1827,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 14,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000607932.5",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "n.630C>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000476506.1",
          "strand": false,
          "transcript": "ENST00000607932.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2036,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 16,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000608057.5",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "n.630C>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000476371.1",
          "strand": false,
          "transcript": "ENST00000608057.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3145,
          "cdna_start": 1284,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000653241.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499476.1",
          "strand": false,
          "transcript": "ENST00000653241.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3044,
          "cdna_start": 1338,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 20,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000655761.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499635.1",
          "strand": false,
          "transcript": "ENST00000655761.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3091,
          "cdna_start": 1383,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000664366.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499290.1",
          "strand": false,
          "transcript": "ENST00000664366.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2877,
          "cdna_start": 1189,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000668382.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499546.1",
          "strand": false,
          "transcript": "ENST00000668382.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3218,
          "cdna_start": 1390,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000867252.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537311.1",
          "strand": false,
          "transcript": "ENST00000867252.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2962,
          "cdna_start": 1243,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000867254.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537313.1",
          "strand": false,
          "transcript": "ENST00000867254.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3004,
          "cdna_start": 1028,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000928342.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598401.1",
          "strand": false,
          "transcript": "ENST00000928342.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3261,
          "cdna_start": 1281,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000928344.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598403.1",
          "strand": false,
          "transcript": "ENST00000928344.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2775,
          "cdna_start": 1062,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000928345.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598404.1",
          "strand": false,
          "transcript": "ENST00000928345.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5930,
          "cdna_start": 3949,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000928346.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000598405.1",
          "strand": false,
          "transcript": "ENST00000928346.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3031,
          "cdna_start": 1057,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000947757.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000617816.1",
          "strand": false,
          "transcript": "ENST00000947757.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 634,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3003,
          "cdna_start": 1029,
          "cds_end": null,
          "cds_length": 1905,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000947758.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000617817.1",
          "strand": false,
          "transcript": "ENST00000947758.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 629,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3059,
          "cdna_start": 1098,
          "cds_end": null,
          "cds_length": 1890,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000947756.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000617815.1",
          "strand": false,
          "transcript": "ENST00000947756.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 559,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2476,
          "cdna_start": 1066,
          "cds_end": null,
          "cds_length": 1680,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000654766.1",
          "gene_hgnc_id": 17284,
          "gene_symbol": "POT1",
          "hgvs_c": "c.630C>T",
          "hgvs_p": "p.Ile210Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000499395.1",
          "strand": false,
          "transcript": "ENST00000654766.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 559,
          "aa_ref": "I",
          "aa_start": 210,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2956,
          "cdna_start": 1204,
          "cds_end": null,
          "cds_length": 1680,
          "cds_start": 630,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000928341.1",
          "gene_hgnc_id": 17284,
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}
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