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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: 19-36103782-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=36103782&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 36103782,
      "ref": "C",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "ENST00000401500.7",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3954C>G",
          "hgvs_p": "p.Gly1318Gly",
          "transcript": "NM_001083961.2",
          "protein_id": "NP_001077430.1",
          "transcript_support_level": null,
          "aa_start": 1318,
          "aa_end": null,
          "aa_length": 1523,
          "cds_start": 3954,
          "cds_end": null,
          "cds_length": 4572,
          "cdna_start": 4029,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "ENST00000401500.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3954C>G",
          "hgvs_p": "p.Gly1318Gly",
          "transcript": "ENST00000401500.7",
          "protein_id": "ENSP00000384792.1",
          "transcript_support_level": 1,
          "aa_start": 1318,
          "aa_end": null,
          "aa_length": 1523,
          "cds_start": 3954,
          "cds_end": null,
          "cds_length": 4572,
          "cdna_start": 4029,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "NM_001083961.2",
          "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": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "n.*3814C>G",
          "hgvs_p": null,
          "transcript": "ENST00000587391.6",
          "protein_id": "ENSP00000465525.1",
          "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": 5973,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "n.*3814C>G",
          "hgvs_p": null,
          "transcript": "ENST00000587391.6",
          "protein_id": "ENSP00000465525.1",
          "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": 5973,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3948C>G",
          "hgvs_p": "p.Gly1316Gly",
          "transcript": "ENST00000679714.1",
          "protein_id": "ENSP00000506627.1",
          "transcript_support_level": null,
          "aa_start": 1316,
          "aa_end": null,
          "aa_length": 1521,
          "cds_start": 3948,
          "cds_end": null,
          "cds_length": 4566,
          "cdna_start": 4023,
          "cdna_end": null,
          "cdna_length": 4708,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3939C>G",
          "hgvs_p": "p.Gly1313Gly",
          "transcript": "NM_001411145.1",
          "protein_id": "NP_001398074.1",
          "transcript_support_level": null,
          "aa_start": 1313,
          "aa_end": null,
          "aa_length": 1518,
          "cds_start": 3939,
          "cds_end": null,
          "cds_length": 4557,
          "cdna_start": 4014,
          "cdna_end": null,
          "cdna_length": 4712,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3939C>G",
          "hgvs_p": "p.Gly1313Gly",
          "transcript": "NM_173636.5",
          "protein_id": "NP_775907.4",
          "transcript_support_level": null,
          "aa_start": 1313,
          "aa_end": null,
          "aa_length": 1518,
          "cds_start": 3939,
          "cds_end": null,
          "cds_length": 4557,
          "cdna_start": 4014,
          "cdna_end": null,
          "cdna_length": 4712,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3939C>G",
          "hgvs_p": "p.Gly1313Gly",
          "transcript": "ENST00000270301.12",
          "protein_id": "ENSP00000270301.6",
          "transcript_support_level": 5,
          "aa_start": 1313,
          "aa_end": null,
          "aa_length": 1518,
          "cds_start": 3939,
          "cds_end": null,
          "cds_length": 4557,
          "cdna_start": 3939,
          "cdna_end": null,
          "cdna_length": 4634,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3939C>G",
          "hgvs_p": "p.Gly1313Gly",
          "transcript": "ENST00000679682.1",
          "protein_id": "ENSP00000506226.1",
          "transcript_support_level": null,
          "aa_start": 1313,
          "aa_end": null,
          "aa_length": 1518,
          "cds_start": 3939,
          "cds_end": null,
          "cds_length": 4557,
          "cdna_start": 4014,
          "cdna_end": null,
          "cdna_length": 4702,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3705C>G",
          "hgvs_p": "p.Gly1235Gly",
          "transcript": "NM_001411146.1",
          "protein_id": "NP_001398075.1",
          "transcript_support_level": null,
          "aa_start": 1235,
          "aa_end": null,
          "aa_length": 1440,
          "cds_start": 3705,
          "cds_end": null,
          "cds_length": 4323,
          "cdna_start": 3780,
          "cdna_end": null,
          "cdna_length": 4478,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3705C>G",
          "hgvs_p": "p.Gly1235Gly",
          "transcript": "ENST00000680564.1",
          "protein_id": "ENSP00000505582.1",
          "transcript_support_level": null,
          "aa_start": 1235,
          "aa_end": null,
          "aa_length": 1440,
          "cds_start": 3705,
          "cds_end": null,
          "cds_length": 4323,
          "cdna_start": 3780,
          "cdna_end": null,
          "cdna_length": 4478,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3939C>G",
          "hgvs_p": "p.Gly1313Gly",
          "transcript": "ENST00000680403.1",
          "protein_id": "ENSP00000505677.1",
          "transcript_support_level": null,
          "aa_start": 1313,
          "aa_end": null,
          "aa_length": 1434,
          "cds_start": 3939,
          "cds_end": null,
          "cds_length": 4305,
          "cdna_start": 4014,
          "cdna_end": null,
          "cdna_length": 4627,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3603C>G",
          "hgvs_p": "p.Gly1201Gly",
          "transcript": "NM_001411147.1",
          "protein_id": "NP_001398076.1",
          "transcript_support_level": null,
          "aa_start": 1201,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": 3603,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": 3678,
          "cdna_end": null,
          "cdna_length": 4376,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3603C>G",
          "hgvs_p": "p.Gly1201Gly",
          "transcript": "ENST00000679757.1",
          "protein_id": "ENSP00000505158.1",
          "transcript_support_level": null,
          "aa_start": 1201,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": 3603,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": 3645,
          "cdna_end": null,
          "cdna_length": 4339,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.555C>G",
          "hgvs_p": "p.Gly185Gly",
          "transcript": "ENST00000680211.1",
          "protein_id": "ENSP00000506102.1",
          "transcript_support_level": null,
          "aa_start": 185,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 555,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 1368,
          "cdna_end": null,
          "cdna_length": 2066,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3954C>G",
          "hgvs_p": "p.Gly1318Gly",
          "transcript": "XM_017026665.2",
          "protein_id": "XP_016882154.1",
          "transcript_support_level": null,
          "aa_start": 1318,
          "aa_end": null,
          "aa_length": 1523,
          "cds_start": 3954,
          "cds_end": null,
          "cds_length": 4572,
          "cdna_start": 4029,
          "cdna_end": null,
          "cdna_length": 4709,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3924C>G",
          "hgvs_p": "p.Gly1308Gly",
          "transcript": "XM_047438657.1",
          "protein_id": "XP_047294613.1",
          "transcript_support_level": null,
          "aa_start": 1308,
          "aa_end": null,
          "aa_length": 1513,
          "cds_start": 3924,
          "cds_end": null,
          "cds_length": 4542,
          "cdna_start": 3999,
          "cdna_end": null,
          "cdna_length": 4697,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3843C>G",
          "hgvs_p": "p.Gly1281Gly",
          "transcript": "XM_005258809.3",
          "protein_id": "XP_005258866.1",
          "transcript_support_level": null,
          "aa_start": 1281,
          "aa_end": null,
          "aa_length": 1486,
          "cds_start": 3843,
          "cds_end": null,
          "cds_length": 4461,
          "cdna_start": 3918,
          "cdna_end": null,
          "cdna_length": 4616,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3828C>G",
          "hgvs_p": "p.Gly1276Gly",
          "transcript": "XM_047438658.1",
          "protein_id": "XP_047294614.1",
          "transcript_support_level": null,
          "aa_start": 1276,
          "aa_end": null,
          "aa_length": 1481,
          "cds_start": 3828,
          "cds_end": null,
          "cds_length": 4446,
          "cdna_start": 3903,
          "cdna_end": null,
          "cdna_length": 4601,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WDR62",
          "gene_hgnc_id": 24502,
          "hgvs_c": "c.3828C>G",
          "hgvs_p": "p.Gly1276Gly",
          "transcript": "XM_047438659.1",
          "protein_id": "XP_047294615.1",
          "transcript_support_level": null,
          "aa_start": 1276,
          "aa_end": null,
          "aa_length": 1481,
          "cds_start": 3828,
          "cds_end": null,
          "cds_length": 4446,
          "cdna_start": 3903,
          "cdna_end": null,
          "cdna_length": 4601,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
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      "gene_symbol": "WDR62",
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      "computational_score_selected": -0.7799999713897705,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "bayesdelnoaf_score": -0.78,
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      "phylop100way_score": -0.1,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_score": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
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          "pathogenic_score": 2,
          "criteria": [
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            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
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          "verdict": "Likely_benign",
          "transcript": "ENST00000401500.7",
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          "effects": [
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          "inheritance_mode": "AR",
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          "hgvs_p": "p.Gly1318Gly"
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}