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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: 3-9448586-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=9448586&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 9448586,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000402198.7",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg",
          "transcript": "NM_001080517.3",
          "protein_id": "NP_001073986.1",
          "transcript_support_level": null,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 1442,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 4329,
          "cdna_start": 2841,
          "cdna_end": null,
          "cdna_length": 6931,
          "mane_select": "ENST00000402198.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg",
          "transcript": "ENST00000402198.7",
          "protein_id": "ENSP00000385852.2",
          "transcript_support_level": 5,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 1442,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 4329,
          "cdna_start": 2841,
          "cdna_end": null,
          "cdna_length": 6931,
          "mane_select": "NM_001080517.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "n.2466C>A",
          "hgvs_p": null,
          "transcript": "ENST00000493918.5",
          "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": 4861,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2359C>A",
          "hgvs_p": "p.Arg787Arg",
          "transcript": "NM_001437635.1",
          "protein_id": "NP_001424564.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 1480,
          "cds_start": 2359,
          "cds_end": null,
          "cds_length": 4443,
          "cdna_start": 2898,
          "cdna_end": null,
          "cdna_length": 7037,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2398C>A",
          "hgvs_p": "p.Arg800Arg",
          "transcript": "NM_001437633.1",
          "protein_id": "NP_001424562.1",
          "transcript_support_level": null,
          "aa_start": 800,
          "aa_end": null,
          "aa_length": 1474,
          "cds_start": 2398,
          "cds_end": null,
          "cds_length": 4425,
          "cdna_start": 2937,
          "cdna_end": null,
          "cdna_length": 7019,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2398C>A",
          "hgvs_p": "p.Arg800Arg",
          "transcript": "ENST00000682536.1",
          "protein_id": "ENSP00000507956.1",
          "transcript_support_level": null,
          "aa_start": 800,
          "aa_end": null,
          "aa_length": 1474,
          "cds_start": 2398,
          "cds_end": null,
          "cds_length": 4425,
          "cdna_start": 2671,
          "cdna_end": null,
          "cdna_length": 5624,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg",
          "transcript": "NM_001437643.1",
          "protein_id": "NP_001424572.1",
          "transcript_support_level": null,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 1461,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 4386,
          "cdna_start": 3376,
          "cdna_end": null,
          "cdna_length": 7515,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2359C>A",
          "hgvs_p": "p.Arg787Arg",
          "transcript": "ENST00000407969.5",
          "protein_id": "ENSP00000384114.1",
          "transcript_support_level": 5,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 1461,
          "cds_start": 2359,
          "cds_end": null,
          "cds_length": 4386,
          "cdna_start": 2373,
          "cdna_end": null,
          "cdna_length": 6463,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2341C>A",
          "hgvs_p": "p.Arg781Arg",
          "transcript": "NM_001437701.1",
          "protein_id": "NP_001424630.1",
          "transcript_support_level": null,
          "aa_start": 781,
          "aa_end": null,
          "aa_length": 1455,
          "cds_start": 2341,
          "cds_end": null,
          "cds_length": 4368,
          "cdna_start": 2880,
          "cdna_end": null,
          "cdna_length": 6962,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg",
          "transcript": "ENST00000406341.5",
          "protein_id": "ENSP00000383939.1",
          "transcript_support_level": 5,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 1442,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 4329,
          "cdna_start": 2492,
          "cdna_end": null,
          "cdna_length": 6582,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2008C>A",
          "hgvs_p": "p.Arg670Arg",
          "transcript": "NM_001292043.2",
          "protein_id": "NP_001278972.1",
          "transcript_support_level": null,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1344,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 4035,
          "cdna_start": 3105,
          "cdna_end": null,
          "cdna_length": 7187,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2008C>A",
          "hgvs_p": "p.Arg670Arg",
          "transcript": "NM_001349451.2",
          "protein_id": "NP_001336380.1",
          "transcript_support_level": null,
          "aa_start": 670,
          "aa_end": null,
          "aa_length": 1344,
          "cds_start": 2008,
          "cds_end": null,
          "cds_length": 4035,
          "cdna_start": 3146,
          "cdna_end": null,
          "cdna_length": 7228,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg",
          "transcript": "ENST00000684055.1",
          "protein_id": "ENSP00000507953.1",
          "transcript_support_level": null,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 931,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 2796,
          "cdna_start": 2418,
          "cdna_end": null,
          "cdna_length": 4416,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.1303C>A",
          "hgvs_p": "p.Arg435Arg",
          "transcript": "ENST00000399686.6",
          "protein_id": "ENSP00000382593.2",
          "transcript_support_level": 5,
          "aa_start": 435,
          "aa_end": null,
          "aa_length": 910,
          "cds_start": 1303,
          "cds_end": null,
          "cds_length": 2733,
          "cdna_start": 1304,
          "cdna_end": null,
          "cdna_length": 3362,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.235C>A",
          "hgvs_p": "p.Arg79Arg",
          "transcript": "ENST00000421188.1",
          "protein_id": "ENSP00000399993.1",
          "transcript_support_level": 5,
          "aa_start": 79,
          "aa_end": null,
          "aa_length": 439,
          "cds_start": 235,
          "cds_end": null,
          "cds_length": 1322,
          "cdna_start": 236,
          "cdna_end": null,
          "cdna_length": 1323,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.517C>A",
          "hgvs_p": "p.Arg173Arg",
          "transcript": "ENST00000488236.5",
          "protein_id": "ENSP00000507801.1",
          "transcript_support_level": 5,
          "aa_start": 173,
          "aa_end": null,
          "aa_length": 249,
          "cds_start": 517,
          "cds_end": null,
          "cds_length": 750,
          "cdna_start": 519,
          "cdna_end": null,
          "cdna_length": 1320,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2419C>A",
          "hgvs_p": "p.Arg807Arg",
          "transcript": "XM_047448466.1",
          "protein_id": "XP_047304422.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 1500,
          "cds_start": 2419,
          "cds_end": null,
          "cds_length": 4503,
          "cdna_start": 7490,
          "cdna_end": null,
          "cdna_length": 11637,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2419C>A",
          "hgvs_p": "p.Arg807Arg",
          "transcript": "XM_047448467.1",
          "protein_id": "XP_047304423.1",
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          "aa_start": 807,
          "aa_end": null,
          "aa_length": 1500,
          "cds_start": 2419,
          "cds_end": null,
          "cds_length": 4503,
          "cdna_start": 6462,
          "cdna_end": null,
          "cdna_length": 10609,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2419C>A",
          "hgvs_p": "p.Arg807Arg",
          "transcript": "XM_047448468.1",
          "protein_id": "XP_047304424.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 1500,
          "cds_start": 2419,
          "cds_end": null,
          "cds_length": 4503,
          "cdna_start": 8430,
          "cdna_end": null,
          "cdna_length": 12577,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
          "gene_hgnc_id": 25566,
          "hgvs_c": "c.2419C>A",
          "hgvs_p": "p.Arg807Arg",
          "transcript": "XM_047448469.1",
          "protein_id": "XP_047304425.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 1500,
          "cds_start": 2419,
          "cds_end": null,
          "cds_length": 4503,
          "cdna_start": 4353,
          "cdna_end": null,
          "cdna_length": 8500,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD5",
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      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.34,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 3.008,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.02,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP7",
            "BS2"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000402198.7",
          "gene_symbol": "SETD5",
          "hgnc_id": 25566,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2302C>A",
          "hgvs_p": "p.Arg768Arg"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}