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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: 7-5978684-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=5978684&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 5978684,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000265849.12",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2187C>T",
          "hgvs_p": "p.Leu729Leu",
          "transcript": "NM_000535.7",
          "protein_id": "NP_000526.2",
          "transcript_support_level": null,
          "aa_start": 729,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 2187,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 2217,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "ENST00000265849.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2187C>T",
          "hgvs_p": "p.Leu729Leu",
          "transcript": "ENST00000265849.12",
          "protein_id": "ENSP00000265849.7",
          "transcript_support_level": 1,
          "aa_start": 729,
          "aa_end": null,
          "aa_length": 862,
          "cds_start": 2187,
          "cds_end": null,
          "cds_length": 2589,
          "cdna_start": 2217,
          "cdna_end": null,
          "cdna_length": 5093,
          "mane_select": "NM_000535.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.984C>T",
          "hgvs_p": "p.Leu328Leu",
          "transcript": "ENST00000382321.5",
          "protein_id": "ENSP00000371758.4",
          "transcript_support_level": 1,
          "aa_start": 328,
          "aa_end": null,
          "aa_length": 461,
          "cds_start": 984,
          "cds_end": null,
          "cds_length": 1386,
          "cdna_start": 984,
          "cdna_end": null,
          "cdna_length": 1386,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "n.1679-970C>T",
          "hgvs_p": null,
          "transcript": "ENST00000406569.8",
          "protein_id": "ENSP00000514464.1",
          "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": 2101,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2373C>T",
          "hgvs_p": "p.Leu791Leu",
          "transcript": "NM_001406866.1",
          "protein_id": "NP_001393795.1",
          "transcript_support_level": null,
          "aa_start": 791,
          "aa_end": null,
          "aa_length": 924,
          "cds_start": 2373,
          "cds_end": null,
          "cds_length": 2775,
          "cdna_start": 2403,
          "cdna_end": null,
          "cdna_length": 5279,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2373C>T",
          "hgvs_p": "p.Leu791Leu",
          "transcript": "ENST00000699839.1",
          "protein_id": "ENSP00000514637.1",
          "transcript_support_level": null,
          "aa_start": 791,
          "aa_end": null,
          "aa_length": 924,
          "cds_start": 2373,
          "cds_end": null,
          "cds_length": 2775,
          "cdna_start": 2438,
          "cdna_end": null,
          "cdna_length": 3597,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2187C>T",
          "hgvs_p": "p.Leu729Leu",
          "transcript": "NM_001322014.2",
          "protein_id": "NP_001308943.1",
          "transcript_support_level": null,
          "aa_start": 729,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 2187,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": 2217,
          "cdna_end": null,
          "cdna_length": 5126,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2187C>T",
          "hgvs_p": "p.Leu729Leu",
          "transcript": "ENST00000699766.1",
          "protein_id": "ENSP00000514574.1",
          "transcript_support_level": null,
          "aa_start": 729,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 2187,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": 2290,
          "cdna_end": null,
          "cdna_length": 5167,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2211C>T",
          "hgvs_p": "p.Leu737Leu",
          "transcript": "NM_001406868.1",
          "protein_id": "NP_001393797.1",
          "transcript_support_level": null,
          "aa_start": 737,
          "aa_end": null,
          "aa_length": 870,
          "cds_start": 2211,
          "cds_end": null,
          "cds_length": 2613,
          "cdna_start": 2241,
          "cdna_end": null,
          "cdna_length": 5117,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2184C>T",
          "hgvs_p": "p.Leu728Leu",
          "transcript": "ENST00000699840.2",
          "protein_id": "ENSP00000514638.2",
          "transcript_support_level": null,
          "aa_start": 728,
          "aa_end": null,
          "aa_length": 861,
          "cds_start": 2184,
          "cds_end": null,
          "cds_length": 2586,
          "cdna_start": 2252,
          "cdna_end": null,
          "cdna_length": 2812,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2079C>T",
          "hgvs_p": "p.Leu693Leu",
          "transcript": "NM_001406869.1",
          "protein_id": "NP_001393798.1",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 2079,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": 2109,
          "cdna_end": null,
          "cdna_length": 4985,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2079C>T",
          "hgvs_p": "p.Leu693Leu",
          "transcript": "ENST00000699930.2",
          "protein_id": "ENSP00000514695.2",
          "transcript_support_level": null,
          "aa_start": 693,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 2079,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": 2159,
          "cdna_end": null,
          "cdna_length": 5035,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2031C>T",
          "hgvs_p": "p.Leu677Leu",
          "transcript": "NM_001406870.1",
          "protein_id": "NP_001393799.1",
          "transcript_support_level": null,
          "aa_start": 677,
          "aa_end": null,
          "aa_length": 821,
          "cds_start": 2031,
          "cds_end": null,
          "cds_length": 2466,
          "cdna_start": 2061,
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          "cdna_length": 4970,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2031C>T",
          "hgvs_p": "p.Leu677Leu",
          "transcript": "NM_001322006.2",
          "protein_id": "NP_001308935.1",
          "transcript_support_level": null,
          "aa_start": 677,
          "aa_end": null,
          "aa_length": 810,
          "cds_start": 2031,
          "cds_end": null,
          "cds_length": 2433,
          "cdna_start": 2061,
          "cdna_end": null,
          "cdna_length": 4937,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2031C>T",
          "hgvs_p": "p.Leu677Leu",
          "transcript": "ENST00000699752.1",
          "protein_id": "ENSP00000514561.1",
          "transcript_support_level": null,
          "aa_start": 677,
          "aa_end": null,
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          "cds_start": 2031,
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          "cdna_start": 2061,
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          "cdna_length": 4907,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2019C>T",
          "hgvs_p": "p.Leu673Leu",
          "transcript": "NM_001406872.1",
          "protein_id": "NP_001393801.1",
          "transcript_support_level": null,
          "aa_start": 673,
          "aa_end": null,
          "aa_length": 806,
          "cds_start": 2019,
          "cds_end": null,
          "cds_length": 2421,
          "cdna_start": 2049,
          "cdna_end": null,
          "cdna_length": 4925,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2019C>T",
          "hgvs_p": "p.Leu673Leu",
          "transcript": "NM_001406874.1",
          "protein_id": "NP_001393803.1",
          "transcript_support_level": null,
          "aa_start": 673,
          "aa_end": null,
          "aa_length": 806,
          "cds_start": 2019,
          "cds_end": null,
          "cds_length": 2421,
          "cdna_start": 2049,
          "cdna_end": null,
          "cdna_length": 4925,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.2019C>T",
          "hgvs_p": "p.Leu673Leu",
          "transcript": "ENST00000699827.1",
          "protein_id": "ENSP00000514628.1",
          "transcript_support_level": null,
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          "cds_start": 2019,
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          "cdna_start": 2099,
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          "cdna_length": 2659,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.1989C>T",
          "hgvs_p": "p.Leu663Leu",
          "transcript": "NM_001406873.1",
          "protein_id": "NP_001393802.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 796,
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          "cds_length": 2391,
          "cdna_start": 2019,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PMS2",
          "gene_hgnc_id": 9122,
          "hgvs_c": "c.1989C>T",
          "hgvs_p": "p.Leu663Leu",
          "transcript": "ENST00000699754.1",
          "protein_id": "ENSP00000514563.1",
          "transcript_support_level": null,
          "aa_start": 663,
          "aa_end": null,
          "aa_length": 796,
          "cds_start": 1989,
          "cds_end": null,
          "cds_length": 2391,
          "cdna_start": 2034,
          "cdna_end": null,
          "cdna_length": 4880,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
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          "hgvs_p": "p.Leu729Leu"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}