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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: 20-32434812-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=32434812&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 32434812,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000375687.10",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2100T>C",
          "hgvs_p": "p.Tyr700Tyr",
          "transcript": "NM_015338.6",
          "protein_id": "NP_056153.2",
          "transcript_support_level": null,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 1541,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 4626,
          "cdna_start": 2545,
          "cdna_end": null,
          "cdna_length": 7052,
          "mane_select": "ENST00000375687.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2100T>C",
          "hgvs_p": "p.Tyr700Tyr",
          "transcript": "ENST00000375687.10",
          "protein_id": "ENSP00000364839.4",
          "transcript_support_level": 5,
          "aa_start": 700,
          "aa_end": null,
          "aa_length": 1541,
          "cds_start": 2100,
          "cds_end": null,
          "cds_length": 4626,
          "cdna_start": 2545,
          "cdna_end": null,
          "cdna_length": 7052,
          "mane_select": "NM_015338.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2085T>C",
          "hgvs_p": "p.Tyr695Tyr",
          "transcript": "ENST00000306058.9",
          "protein_id": "ENSP00000305119.5",
          "transcript_support_level": 1,
          "aa_start": 695,
          "aa_end": null,
          "aa_length": 1536,
          "cds_start": 2085,
          "cds_end": null,
          "cds_length": 4611,
          "cdna_start": 2085,
          "cdna_end": null,
          "cdna_length": 6591,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.1917T>C",
          "hgvs_p": "p.Tyr639Tyr",
          "transcript": "NM_001363734.1",
          "protein_id": "NP_001350663.1",
          "transcript_support_level": null,
          "aa_start": 639,
          "aa_end": null,
          "aa_length": 1480,
          "cds_start": 1917,
          "cds_end": null,
          "cds_length": 4443,
          "cdna_start": 2160,
          "cdna_end": null,
          "cdna_length": 6667,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.1917T>C",
          "hgvs_p": "p.Tyr639Tyr",
          "transcript": "ENST00000646985.1",
          "protein_id": "ENSP00000495053.1",
          "transcript_support_level": null,
          "aa_start": 639,
          "aa_end": null,
          "aa_length": 1480,
          "cds_start": 1917,
          "cds_end": null,
          "cds_length": 4443,
          "cdna_start": 2160,
          "cdna_end": null,
          "cdna_length": 6666,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2361T>C",
          "hgvs_p": "p.Tyr787Tyr",
          "transcript": "XM_011528648.4",
          "protein_id": "XP_011526950.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 1628,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 4887,
          "cdna_start": 2389,
          "cdna_end": null,
          "cdna_length": 6896,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2097T>C",
          "hgvs_p": "p.Tyr699Tyr",
          "transcript": "XM_006723727.4",
          "protein_id": "XP_006723790.1",
          "transcript_support_level": null,
          "aa_start": 699,
          "aa_end": null,
          "aa_length": 1540,
          "cds_start": 2097,
          "cds_end": null,
          "cds_length": 4623,
          "cdna_start": 2542,
          "cdna_end": null,
          "cdna_length": 7049,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2079T>C",
          "hgvs_p": "p.Tyr693Tyr",
          "transcript": "XM_047439939.1",
          "protein_id": "XP_047295895.1",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 1534,
          "cds_start": 2079,
          "cds_end": null,
          "cds_length": 4605,
          "cdna_start": 2322,
          "cdna_end": null,
          "cdna_length": 6829,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2070T>C",
          "hgvs_p": "p.Tyr690Tyr",
          "transcript": "XM_006723728.4",
          "protein_id": "XP_006723791.1",
          "transcript_support_level": null,
          "aa_start": 690,
          "aa_end": null,
          "aa_length": 1531,
          "cds_start": 2070,
          "cds_end": null,
          "cds_length": 4596,
          "cdna_start": 2313,
          "cdna_end": null,
          "cdna_length": 6820,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2067T>C",
          "hgvs_p": "p.Tyr689Tyr",
          "transcript": "XM_047439940.1",
          "protein_id": "XP_047295896.1",
          "transcript_support_level": null,
          "aa_start": 689,
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          "aa_length": 1530,
          "cds_start": 2067,
          "cds_end": null,
          "cds_length": 4593,
          "cdna_start": 2310,
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          "mane_select": null,
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        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 13,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2016T>C",
          "hgvs_p": "p.Tyr672Tyr",
          "transcript": "XM_006723730.5",
          "protein_id": "XP_006723793.1",
          "transcript_support_level": null,
          "aa_start": 672,
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          "cds_start": 2016,
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          "cds_length": 4542,
          "cdna_start": 2413,
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          "mane_select": null,
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 14,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
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        },
        {
          "aa_ref": "Y",
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          ],
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          "gene_symbol": "ASXL1",
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          "hgvs_c": "c.2016T>C",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.2016T>C",
          "hgvs_p": "p.Tyr672Tyr",
          "transcript": "XM_047439943.1",
          "protein_id": "XP_047295899.1",
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        },
        {
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          ],
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          "hgvs_c": "c.2016T>C",
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        },
        {
          "aa_ref": "Y",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.1944T>C",
          "hgvs_p": "p.Tyr648Tyr",
          "transcript": "XM_047439945.1",
          "protein_id": "XP_047295901.1",
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.1416T>C",
          "hgvs_p": "p.Tyr472Tyr",
          "transcript": "XM_006723733.2",
          "protein_id": "XP_006723796.1",
          "transcript_support_level": null,
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          "cds_start": 1416,
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        },
        {
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          "strand": true,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "n.4453T>C",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": 13,
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          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "c.1869+231T>C",
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          "transcript": "ENST00000651418.1",
          "protein_id": "ENSP00000499150.1",
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          "cds_start": -4,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ASXL1",
          "gene_hgnc_id": 18318,
          "hgvs_c": "n.*176T>C",
          "hgvs_p": null,
          "transcript": "ENST00000644168.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1466,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ASXL1",
      "gene_hgnc_id": 18318,
      "dbsnp": "rs1261178797",
      "frequency_reference_population": 0.0000065739305,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000657393,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6600000262260437,
      "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": -0.66,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.265,
      "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": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000375687.10",
          "gene_symbol": "ASXL1",
          "hgnc_id": 18318,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2100T>C",
          "hgvs_p": "p.Tyr700Tyr"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}