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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: 11-17330136-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=17330136&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "stop_gained"
          ],
          "gene_symbol": "NUCB2",
          "hgnc_id": 8044,
          "hgvs_c": "c.1015C>T",
          "hgvs_p": "p.Gln339*",
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "NM_001352661.2",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_score": 0,
      "allele_count_reference_population": null,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Pathogenic",
      "bayesdelnoaf_score": 0.65,
      "chr": "11",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": 0.1340000033378601,
      "computational_source_selected": "REVEL",
      "consequences": [
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2300,
          "cdna_start": 1257,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "NM_005013.4",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000529010.6",
          "protein_coding": true,
          "protein_id": "NP_005004.1",
          "strand": true,
          "transcript": "NM_005013.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 2300,
          "cdna_start": 1257,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000529010.6",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_005013.4",
          "protein_coding": true,
          "protein_id": "ENSP00000436455.1",
          "strand": true,
          "transcript": "ENST00000529010.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 2746,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 17,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000646648.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "n.*324C>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000495210.1",
          "strand": true,
          "transcript": "ENST00000646648.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 2746,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 17,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "ENST00000646648.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "n.*324C>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000495210.1",
          "strand": true,
          "transcript": "ENST00000646648.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 438,
          "aa_ref": "Q",
          "aa_start": 356,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1670,
          "cdna_start": 1314,
          "cds_end": null,
          "cds_length": 1317,
          "cds_start": 1066,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000909741.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1066C>T",
          "hgvs_p": "p.Gln356*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000579800.1",
          "strand": true,
          "transcript": "ENST00000909741.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 438,
          "aa_ref": "Q",
          "aa_start": 356,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1811,
          "cdna_start": 1430,
          "cds_end": null,
          "cds_length": 1317,
          "cds_start": 1066,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 15,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "ENST00000935684.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1066C>T",
          "hgvs_p": "p.Gln356*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000605743.1",
          "strand": true,
          "transcript": "ENST00000935684.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 430,
          "aa_ref": "Q",
          "aa_start": 348,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1676,
          "cdna_start": 1328,
          "cds_end": null,
          "cds_length": 1293,
          "cds_start": 1042,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000909731.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1042C>T",
          "hgvs_p": "p.Gln348*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000579790.1",
          "strand": true,
          "transcript": "ENST00000909731.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 421,
          "aa_ref": "Q",
          "aa_start": 339,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2510,
          "cdna_start": 1467,
          "cds_end": null,
          "cds_length": 1266,
          "cds_start": 1015,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 16,
          "exon_rank": 14,
          "exon_rank_end": null,
          "feature": "NM_001352661.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1015C>T",
          "hgvs_p": "p.Gln339*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339590.1",
          "strand": true,
          "transcript": "NM_001352661.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 421,
          "aa_ref": "Q",
          "aa_start": 339,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2426,
          "cdna_start": 1383,
          "cds_end": null,
          "cds_length": 1266,
          "cds_start": 1015,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 15,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001352663.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1015C>T",
          "hgvs_p": "p.Gln339*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339592.1",
          "strand": true,
          "transcript": "NM_001352663.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2380,
          "cdna_start": 1337,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 15,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001352664.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339593.1",
          "strand": true,
          "transcript": "NM_001352664.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2320,
          "cdna_start": 1277,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "NM_001352668.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339597.1",
          "strand": true,
          "transcript": "NM_001352668.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2384,
          "cdna_start": 1341,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 15,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001352669.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339598.1",
          "strand": true,
          "transcript": "NM_001352669.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2283,
          "cdna_start": 1240,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "NM_001352670.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339599.1",
          "strand": true,
          "transcript": "NM_001352670.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2569,
          "cdna_start": 1526,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 15,
          "exon_rank": 13,
          "exon_rank_end": null,
          "feature": "NM_001352672.2",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001339601.1",
          "strand": true,
          "transcript": "NM_001352672.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1905,
          "cdna_start": 1255,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 13,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000323688.10",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000320168.6",
          "strand": true,
          "transcript": "ENST00000323688.10",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4391,
          "cdna_start": 1110,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 13,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000909713.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000579772.1",
          "strand": true,
          "transcript": "ENST00000909713.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1929,
          "cdna_start": 1232,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000909714.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000579773.1",
          "strand": true,
          "transcript": "ENST00000909714.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2034,
          "cdna_start": 1337,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000909715.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000579774.1",
          "strand": true,
          "transcript": "ENST00000909715.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 420,
          "aa_ref": "Q",
          "aa_start": 338,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3202,
          "cdna_start": 1338,
          "cds_end": null,
          "cds_length": 1263,
          "cds_start": 1012,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 14,
          "exon_rank": 12,
          "exon_rank_end": null,
          "feature": "ENST00000909716.1",
          "gene_hgnc_id": 8044,
          "gene_symbol": "NUCB2",
          "hgvs_c": "c.1012C>T",
          "hgvs_p": "p.Gln338*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
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      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0,
      "transcript": "NM_001352661.2"
    }
  ]
}
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