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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: 1-11020554-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=11020554&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 7,
          "criteria": [
            "BP4_Moderate",
            "BP6",
            "BS2"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "TARDBP",
          "hgnc_id": 11571,
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "inheritance_mode": "AD",
          "pathogenic_score": 0,
          "score": -7,
          "transcript": "NM_007375.4",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6,BS2",
      "acmg_score": -7,
      "allele_count_reference_population": 144,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "G",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.31,
      "chr": "1",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_disease": " TARDBP-RELATED,Amyotrophic lateral sclerosis type 10,FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS,Inborn genetic diseases,TARDBP-related disorder,not provided",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:3 B:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.3100000023841858,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4185,
          "cdna_start": 771,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "NM_007375.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000240185.8",
          "protein_coding": true,
          "protein_id": "NP_031401.1",
          "strand": true,
          "transcript": "NM_007375.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4185,
          "cdna_start": 771,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000240185.8",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_007375.4",
          "protein_coding": true,
          "protein_id": "ENSP00000240185.4",
          "strand": true,
          "transcript": "ENST00000240185.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 269,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 810,
          "cdna_start": 669,
          "cds_end": null,
          "cds_length": 810,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000649624.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000497327.1",
          "strand": true,
          "transcript": "ENST00000649624.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2269,
          "cdna_start": 738,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000639083.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000491203.1",
          "strand": true,
          "transcript": "ENST00000639083.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2719,
          "cdna_start": 754,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000881691.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000551750.1",
          "strand": true,
          "transcript": "ENST00000881691.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6043,
          "cdna_start": 1705,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000913574.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000583633.1",
          "strand": true,
          "transcript": "ENST00000913574.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2842,
          "cdna_start": 875,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000913575.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000583634.1",
          "strand": true,
          "transcript": "ENST00000913575.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2954,
          "cdna_start": 987,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000913577.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000583636.1",
          "strand": true,
          "transcript": "ENST00000913577.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3324,
          "cdna_start": 1363,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000958690.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000628749.1",
          "strand": true,
          "transcript": "ENST00000958690.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 414,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2756,
          "cdna_start": 797,
          "cds_end": null,
          "cds_length": 1245,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000958691.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000628750.1",
          "strand": true,
          "transcript": "ENST00000958691.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 304,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1008,
          "cdna_start": 669,
          "cds_end": null,
          "cds_length": 915,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000621790.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000482191.1",
          "strand": true,
          "transcript": "ENST00000621790.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 301,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 920,
          "cdna_start": 669,
          "cds_end": null,
          "cds_length": 906,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000616545.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000484722.1",
          "strand": true,
          "transcript": "ENST00000616545.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 298,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1031,
          "cdna_start": 803,
          "cds_end": null,
          "cds_length": 897,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 7,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000629725.2",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000486989.1",
          "strand": true,
          "transcript": "ENST00000629725.2",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 295,
          "aa_ref": "P",
          "aa_start": 223,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1835,
          "cdna_start": 681,
          "cds_end": null,
          "cds_length": 888,
          "cds_start": 669,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000315091.7",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.669C>G",
          "hgvs_p": "p.Pro223Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000313129.3",
          "strand": true,
          "transcript": "ENST00000315091.7",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 274,
          "aa_ref": "P",
          "aa_start": 264,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 929,
          "cdna_start": 894,
          "cds_end": null,
          "cds_length": 827,
          "cds_start": 792,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 6,
          "exon_rank": 6,
          "exon_rank_end": null,
          "feature": "ENST00000476201.5",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.792C>G",
          "hgvs_p": "p.Pro264Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000466842.2",
          "strand": true,
          "transcript": "ENST00000476201.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 211,
          "aa_ref": "P",
          "aa_start": 136,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 980,
          "cdna_start": 410,
          "cds_end": null,
          "cds_length": 636,
          "cds_start": 408,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000617172.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.408C>G",
          "hgvs_p": "p.Pro136Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000479219.1",
          "strand": true,
          "transcript": "ENST00000617172.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 199,
          "aa_ref": "P",
          "aa_start": 138,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 706,
          "cdna_start": 416,
          "cds_end": null,
          "cds_length": 600,
          "cds_start": 414,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000622057.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.414C>G",
          "hgvs_p": "p.Pro138Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000481206.1",
          "strand": true,
          "transcript": "ENST00000622057.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "P",
          "aa_end": null,
          "aa_length": 127,
          "aa_ref": "P",
          "aa_start": 49,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 563,
          "cdna_start": 147,
          "cds_end": null,
          "cds_length": 384,
          "cds_start": 147,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 5,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000610369.4",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
          "hgvs_c": "c.147C>G",
          "hgvs_p": "p.Pro49Pro",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000482559.1",
          "strand": true,
          "transcript": "ENST00000610369.4",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 357,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3531,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1074,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 4,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000913576.1",
          "gene_hgnc_id": 11571,
          "gene_symbol": "TARDBP",
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          "protein_id": "ENSP00000465240.1",
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          "transcript": "ENST00000473118.5",
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        {
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          "biotype": "nonsense_mediated_decay",
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          "cdna_length": 409,
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            "upstream_gene_variant"
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          "feature": "ENST00000477447.6",
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          "hgvs_c": "n.-34C>G",
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          "protein_coding": false,
          "protein_id": "ENSP00000465888.2",
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          "transcript": "ENST00000477447.6",
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      ],
      "custom_annotations": null,
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      "dbsnp": "rs149517613",
      "effect": "synonymous_variant",
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      "gene_hgnc_id": 11571,
      "gene_symbol": "TARDBP",
      "gnomad_exomes_ac": 134,
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      "mitotip_prediction": null,
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      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "phenotype_combined": "Amyotrophic lateral sclerosis type 10;FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED|not provided|Amyotrophic lateral sclerosis type 10|Inborn genetic diseases|TARDBP-related disorder",
      "phylop100way_prediction": "Uncertain_significance",
      "phylop100way_score": 3.783,
      "pos": 11020554,
      "ref": "C",
      "revel_prediction": null,
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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_007375.4"
    }
  ]
}
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