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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: 1-5877267-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=5877267&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 5877267,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000378156.9",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "NM_015102.5",
          "protein_id": "NP_055917.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 2863,
          "cdna_end": null,
          "cdna_length": 4955,
          "mane_select": "ENST00000378156.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "ENST00000378156.9",
          "protein_id": "ENSP00000367398.4",
          "transcript_support_level": 1,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 2863,
          "cdna_end": null,
          "cdna_length": 4955,
          "mane_select": "NM_015102.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*1544G>A",
          "hgvs_p": null,
          "transcript": "ENST00000378169.7",
          "protein_id": "ENSP00000367411.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4213,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*191G>A",
          "hgvs_p": null,
          "transcript": "ENST00000489180.6",
          "protein_id": "ENSP00000423747.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5548,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*1544G>A",
          "hgvs_p": null,
          "transcript": "ENST00000378169.7",
          "protein_id": "ENSP00000367411.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4213,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*191G>A",
          "hgvs_p": null,
          "transcript": "ENST00000489180.6",
          "protein_id": "ENSP00000423747.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5548,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.1107G>A",
          "hgvs_p": "p.Ala369Ala",
          "transcript": "NM_001291594.2",
          "protein_id": "NP_001278523.1",
          "transcript_support_level": null,
          "aa_start": 369,
          "aa_end": null,
          "aa_length": 914,
          "cds_start": 1107,
          "cds_end": null,
          "cds_length": 2745,
          "cdna_start": 2376,
          "cdna_end": null,
          "cdna_length": 4468,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.1104G>A",
          "hgvs_p": "p.Ala368Ala",
          "transcript": "NM_001291593.2",
          "protein_id": "NP_001278522.1",
          "transcript_support_level": null,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 913,
          "cds_start": 1104,
          "cds_end": null,
          "cds_length": 2742,
          "cdna_start": 2553,
          "cdna_end": null,
          "cdna_length": 4645,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_006710563.4",
          "protein_id": "XP_006710626.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 2850,
          "cdna_end": null,
          "cdna_length": 4942,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_011541216.3",
          "protein_id": "XP_011539518.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 3401,
          "cdna_end": null,
          "cdna_length": 5493,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_011541217.3",
          "protein_id": "XP_011539519.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 3265,
          "cdna_end": null,
          "cdna_length": 5357,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_047417535.1",
          "protein_id": "XP_047273491.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 3390,
          "cdna_end": null,
          "cdna_length": 5482,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_047417537.1",
          "protein_id": "XP_047273493.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 2999,
          "cdna_end": null,
          "cdna_length": 5091,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_047417538.1",
          "protein_id": "XP_047273494.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 3299,
          "cdna_end": null,
          "cdna_length": 5391,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_047417546.1",
          "protein_id": "XP_047273502.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 3163,
          "cdna_end": null,
          "cdna_length": 5255,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2640G>A",
          "hgvs_p": "p.Ala880Ala",
          "transcript": "XM_011541213.2",
          "protein_id": "XP_011539515.1",
          "transcript_support_level": null,
          "aa_start": 880,
          "aa_end": null,
          "aa_length": 1425,
          "cds_start": 2640,
          "cds_end": null,
          "cds_length": 4278,
          "cdna_start": 2678,
          "cdna_end": null,
          "cdna_length": 4770,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2643G>A",
          "hgvs_p": "p.Ala881Ala",
          "transcript": "XM_011541214.2",
          "protein_id": "XP_011539516.1",
          "transcript_support_level": null,
          "aa_start": 881,
          "aa_end": null,
          "aa_length": 1412,
          "cds_start": 2643,
          "cds_end": null,
          "cds_length": 4239,
          "cdna_start": 2681,
          "cdna_end": null,
          "cdna_length": 4731,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2640G>A",
          "hgvs_p": "p.Ala880Ala",
          "transcript": "XM_017000996.2",
          "protein_id": "XP_016856485.1",
          "transcript_support_level": null,
          "aa_start": 880,
          "aa_end": null,
          "aa_length": 1411,
          "cds_start": 2640,
          "cds_end": null,
          "cds_length": 4236,
          "cdna_start": 2678,
          "cdna_end": null,
          "cdna_length": 4728,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2532G>A",
          "hgvs_p": "p.Ala844Ala",
          "transcript": "XM_011541215.2",
          "protein_id": "XP_011539517.1",
          "transcript_support_level": null,
          "aa_start": 844,
          "aa_end": null,
          "aa_length": 1389,
          "cds_start": 2532,
          "cds_end": null,
          "cds_length": 4170,
          "cdna_start": 2570,
          "cdna_end": null,
          "cdna_length": 4662,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2301G>A",
          "hgvs_p": "p.Ala767Ala",
          "transcript": "XM_047417555.1",
          "protein_id": "XP_047273511.1",
          "transcript_support_level": null,
          "aa_start": 767,
          "aa_end": null,
          "aa_length": 1312,
          "cds_start": 2301,
          "cds_end": null,
          "cds_length": 3939,
          "cdna_start": 2339,
          "cdna_end": null,
          "cdna_length": 4431,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
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      "computational_score_selected": -0.7400000095367432,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
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      "splice_source_selected": "max_spliceai",
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      "bayesdelnoaf_score": -0.74,
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      "phylop100way_score": -5.703,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
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          "benign_score": 21,
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            "BP7",
            "BA1"
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          "verdict": "Benign",
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      "clinvar_disease": "Nephronophthisis,Nephronophthisis 4,Senior-Loken syndrome 4,not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:8",
      "phenotype_combined": "not specified|Nephronophthisis|Senior-Loken syndrome 4|Nephronophthisis 4|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}