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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: 1-5863955-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=5863955&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 5863955,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000378156.9",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "NM_015102.5",
          "protein_id": "NP_055917.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4295,
          "cdna_end": null,
          "cdna_length": 4955,
          "mane_select": "ENST00000378156.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "ENST00000378156.9",
          "protein_id": "ENSP00000367398.4",
          "transcript_support_level": 1,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4295,
          "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": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*2976C>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": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.2823C>A",
          "hgvs_p": null,
          "transcript": "ENST00000460696.1",
          "protein_id": null,
          "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": 3967,
          "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": 32,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*1886C>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": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*2976C>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": 32,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "n.*1886C>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": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2539C>A",
          "hgvs_p": "p.Arg847Arg",
          "transcript": "NM_001291594.2",
          "protein_id": "NP_001278523.1",
          "transcript_support_level": null,
          "aa_start": 847,
          "aa_end": null,
          "aa_length": 914,
          "cds_start": 2539,
          "cds_end": null,
          "cds_length": 2745,
          "cdna_start": 3808,
          "cdna_end": null,
          "cdna_length": 4468,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.2536C>A",
          "hgvs_p": "p.Arg846Arg",
          "transcript": "NM_001291593.2",
          "protein_id": "NP_001278522.1",
          "transcript_support_level": null,
          "aa_start": 846,
          "aa_end": null,
          "aa_length": 913,
          "cds_start": 2536,
          "cds_end": null,
          "cds_length": 2742,
          "cdna_start": 3985,
          "cdna_end": null,
          "cdna_length": 4645,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_006710563.4",
          "protein_id": "XP_006710626.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4282,
          "cdna_end": null,
          "cdna_length": 4942,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_011541216.3",
          "protein_id": "XP_011539518.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4833,
          "cdna_end": null,
          "cdna_length": 5493,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_011541217.3",
          "protein_id": "XP_011539519.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4697,
          "cdna_end": null,
          "cdna_length": 5357,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_047417535.1",
          "protein_id": "XP_047273491.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4822,
          "cdna_end": null,
          "cdna_length": 5482,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_047417537.1",
          "protein_id": "XP_047273493.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4431,
          "cdna_end": null,
          "cdna_length": 5091,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_047417538.1",
          "protein_id": "XP_047273494.1",
          "transcript_support_level": null,
          "aa_start": 1359,
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          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4731,
          "cdna_end": null,
          "cdna_length": 5391,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4075C>A",
          "hgvs_p": "p.Arg1359Arg",
          "transcript": "XM_047417546.1",
          "protein_id": "XP_047273502.1",
          "transcript_support_level": null,
          "aa_start": 1359,
          "aa_end": null,
          "aa_length": 1426,
          "cds_start": 4075,
          "cds_end": null,
          "cds_length": 4281,
          "cdna_start": 4595,
          "cdna_end": null,
          "cdna_length": 5255,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4072C>A",
          "hgvs_p": "p.Arg1358Arg",
          "transcript": "XM_011541213.2",
          "protein_id": "XP_011539515.1",
          "transcript_support_level": null,
          "aa_start": 1358,
          "aa_end": null,
          "aa_length": 1425,
          "cds_start": 4072,
          "cds_end": null,
          "cds_length": 4278,
          "cdna_start": 4110,
          "cdna_end": null,
          "cdna_length": 4770,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4033C>A",
          "hgvs_p": "p.Arg1345Arg",
          "transcript": "XM_011541214.2",
          "protein_id": "XP_011539516.1",
          "transcript_support_level": null,
          "aa_start": 1345,
          "aa_end": null,
          "aa_length": 1412,
          "cds_start": 4033,
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          "cds_length": 4239,
          "cdna_start": 4071,
          "cdna_end": null,
          "cdna_length": 4731,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.4030C>A",
          "hgvs_p": "p.Arg1344Arg",
          "transcript": "XM_017000996.2",
          "protein_id": "XP_016856485.1",
          "transcript_support_level": null,
          "aa_start": 1344,
          "aa_end": null,
          "aa_length": 1411,
          "cds_start": 4030,
          "cds_end": null,
          "cds_length": 4236,
          "cdna_start": 4068,
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          "cdna_length": 4728,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NPHP4",
          "gene_hgnc_id": 19104,
          "hgvs_c": "c.3964C>A",
          "hgvs_p": "p.Arg1322Arg",
          "transcript": "XM_011541215.2",
          "protein_id": "XP_011539517.1",
          "transcript_support_level": null,
          "aa_start": 1322,
          "aa_end": null,
          "aa_length": 1389,
          "cds_start": 3964,
          "cds_end": null,
          "cds_length": 4170,
          "cdna_start": 4002,
          "cdna_end": null,
          "cdna_length": 4662,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  "message": null
}