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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: 6-31946260-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=31946260&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 31946260,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001710.6",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "NM_001710.6",
          "protein_id": "NP_001701.2",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 764,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2295,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000425368.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001710.6"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000425368.7",
          "protein_id": "ENSP00000416561.2",
          "transcript_support_level": 1,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 764,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2295,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001710.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000425368.7"
        },
        {
          "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": 30,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000244255",
          "gene_hgnc_id": null,
          "hgvs_c": "c.1571-113C>T",
          "hgvs_p": null,
          "transcript": "ENST00000456570.5",
          "protein_id": "ENSP00000410815.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1266,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3801,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000456570.5"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885733.1",
          "protein_id": "ENSP00000555792.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885733.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885731.1",
          "protein_id": "ENSP00000555790.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 792,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2379,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885731.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885715.1",
          "protein_id": "ENSP00000555774.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 789,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2370,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885715.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885713.1",
          "protein_id": "ENSP00000555772.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 784,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2355,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885713.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885728.1",
          "protein_id": "ENSP00000555787.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 783,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2352,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885728.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885716.1",
          "protein_id": "ENSP00000555775.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 777,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2334,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885716.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885719.1",
          "protein_id": "ENSP00000555778.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 775,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 2328,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885719.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885717.1",
          "protein_id": "ENSP00000555776.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 773,
          "cds_start": 39,
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          "cds_length": 2322,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885717.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885730.1",
          "protein_id": "ENSP00000555789.1",
          "transcript_support_level": null,
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          "cds_start": 39,
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          "cds_length": 2319,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        {
          "aa_ref": "P",
          "aa_alt": "P",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "intron_rank": null,
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          "gene_symbol": "CFB",
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          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885712.1",
          "protein_id": "ENSP00000555771.1",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885737.1",
          "protein_id": "ENSP00000555796.1",
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          "biotype": "protein_coding",
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        {
          "aa_ref": "P",
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          ],
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          "gene_symbol": "CFB",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "intron_rank": null,
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          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885720.1",
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        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885721.1",
          "protein_id": "ENSP00000555780.1",
          "transcript_support_level": null,
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          "biotype": "protein_coding",
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        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
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          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
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          "feature": "ENST00000885729.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
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          "strand": true,
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          "gene_symbol": "CFB",
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          "hgvs_p": "p.Pro13Pro",
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          "feature": "ENST00000885725.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 1,
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          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CFB",
          "gene_hgnc_id": 1037,
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro",
          "transcript": "ENST00000885714.1",
          "protein_id": "ENSP00000555773.1",
          "transcript_support_level": null,
          "aa_start": 13,
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          "biotype": "protein_coding",
          "feature": "ENST00000885714.1"
        },
        {
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      ],
      "gene_symbol": "CFB",
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      "dbsnp": null,
      "frequency_reference_population": 6.8456393e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84564e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6000000238418579,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.019999999552965164,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.6,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.335,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.02,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
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      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001710.6",
          "gene_symbol": "CFB",
          "hgnc_id": 1037,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "Unknown,AD,AR",
          "hgvs_c": "c.39C>T",
          "hgvs_p": "p.Pro13Pro"
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        {
          "score": -4,
          "benign_score": 6,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000456570.5",
          "gene_symbol": "ENSG00000244255",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.1571-113C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}