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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: X-111727368-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=111727368&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 111727368,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000394780.8",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro",
          "transcript": "NM_001099922.3",
          "protein_id": "NP_001093392.1",
          "transcript_support_level": null,
          "aa_start": 671,
          "aa_end": null,
          "aa_length": 1137,
          "cds_start": 2013,
          "cds_end": null,
          "cds_length": 3414,
          "cdna_start": 2062,
          "cdna_end": null,
          "cdna_length": 4113,
          "mane_select": "ENST00000394780.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro",
          "transcript": "ENST00000394780.8",
          "protein_id": "ENSP00000378260.3",
          "transcript_support_level": 2,
          "aa_start": 671,
          "aa_end": null,
          "aa_length": 1137,
          "cds_start": 2013,
          "cds_end": null,
          "cds_length": 3414,
          "cdna_start": 2062,
          "cdna_end": null,
          "cdna_length": 4113,
          "mane_select": "NM_001099922.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Pro593Pro",
          "transcript": "NM_001257231.2",
          "protein_id": "NP_001244160.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 1059,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 3180,
          "cdna_start": 2128,
          "cdna_end": null,
          "cdna_length": 4179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro",
          "transcript": "NM_001324292.2",
          "protein_id": "NP_001311221.1",
          "transcript_support_level": null,
          "aa_start": 671,
          "aa_end": null,
          "aa_length": 1058,
          "cds_start": 2013,
          "cds_end": null,
          "cds_length": 3177,
          "cdna_start": 2062,
          "cdna_end": null,
          "cdna_length": 3876,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1839G>A",
          "hgvs_p": "p.Pro613Pro",
          "transcript": "ENST00000623622.2",
          "protein_id": "ENSP00000485624.2",
          "transcript_support_level": 5,
          "aa_start": 613,
          "aa_end": null,
          "aa_length": 1000,
          "cds_start": 1839,
          "cds_end": null,
          "cds_length": 3003,
          "cdna_start": 1908,
          "cdna_end": null,
          "cdna_length": 3413,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1701G>A",
          "hgvs_p": "p.Pro567Pro",
          "transcript": "NM_001257230.2",
          "protein_id": "NP_001244159.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 954,
          "cds_start": 1701,
          "cds_end": null,
          "cds_length": 2865,
          "cdna_start": 1958,
          "cdna_end": null,
          "cdna_length": 3772,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1701G>A",
          "hgvs_p": "p.Pro567Pro",
          "transcript": "NM_001257234.2",
          "protein_id": "NP_001244163.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 954,
          "cds_start": 1701,
          "cds_end": null,
          "cds_length": 2865,
          "cdna_start": 2083,
          "cdna_end": null,
          "cdna_length": 3897,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1701G>A",
          "hgvs_p": "p.Pro567Pro",
          "transcript": "NM_001257237.2",
          "protein_id": "NP_001244166.1",
          "transcript_support_level": null,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 954,
          "cds_start": 1701,
          "cds_end": null,
          "cds_length": 2865,
          "cdna_start": 2187,
          "cdna_end": null,
          "cdna_length": 4001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1701G>A",
          "hgvs_p": "p.Pro567Pro",
          "transcript": "ENST00000436609.5",
          "protein_id": "ENSP00000392990.2",
          "transcript_support_level": 5,
          "aa_start": 567,
          "aa_end": null,
          "aa_length": 954,
          "cds_start": 1701,
          "cds_end": null,
          "cds_length": 2865,
          "cdna_start": 1998,
          "cdna_end": null,
          "cdna_length": 3812,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1527G>A",
          "hgvs_p": "p.Pro509Pro",
          "transcript": "NM_001324293.1",
          "protein_id": "NP_001311222.1",
          "transcript_support_level": null,
          "aa_start": 509,
          "aa_end": null,
          "aa_length": 896,
          "cds_start": 1527,
          "cds_end": null,
          "cds_length": 2691,
          "cdna_start": 2013,
          "cdna_end": null,
          "cdna_length": 3827,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
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          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro",
          "transcript": "XM_011531028.3",
          "protein_id": "XP_011529330.1",
          "transcript_support_level": null,
          "aa_start": 671,
          "aa_end": null,
          "aa_length": 1161,
          "cds_start": 2013,
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          "cds_length": 3486,
          "cdna_start": 2062,
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          "cdna_length": 4185,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
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          "gene_symbol": "ALG13",
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          "hgvs_p": "p.Pro663Pro",
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          "transcript_support_level": null,
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          "cdna_start": 2038,
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          "mane_select": null,
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        {
          "aa_ref": "P",
          "aa_alt": "P",
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          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": 17,
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          "exon_count": 28,
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          "gene_symbol": "ALG13",
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          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro",
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          "protein_id": "XP_016885336.1",
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          "cds_start": 2013,
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        {
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          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1989G>A",
          "hgvs_p": "p.Pro663Pro",
          "transcript": "XM_047442520.1",
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        {
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        {
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          "intron_rank": null,
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          "gene_symbol": "ALG13",
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          "hgvs_c": "c.1842G>A",
          "hgvs_p": "p.Pro614Pro",
          "transcript": "XM_047442521.1",
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        {
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        {
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        {
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        {
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          "gene_symbol": "ALG13",
          "gene_hgnc_id": 30881,
          "hgvs_c": "c.1701G>A",
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          "transcript": "XM_006724698.4",
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        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 17,
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          "intron_rank": null,
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          "gene_symbol": "ALG13",
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      ],
      "gene_symbol": "ALG13",
      "gene_hgnc_id": 30881,
      "dbsnp": "rs775697727",
      "frequency_reference_population": 0.00006127827,
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      "allele_count_reference_population": 74,
      "gnomad_exomes_af": 0.0000629307,
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      "gnomad_exomes_homalt": 0,
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      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8999999761581421,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
      "splice_prediction_selected": null,
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      "revel_score": null,
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      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.9,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.374,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
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      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -17,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -17,
          "benign_score": 17,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000394780.8",
          "gene_symbol": "ALG13",
          "hgnc_id": 30881,
          "effects": [
            "synonymous_variant"
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          "inheritance_mode": "XL",
          "hgvs_c": "c.2013G>A",
          "hgvs_p": "p.Pro671Pro"
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      ],
      "clinvar_disease": " 36,Developmental and epileptic encephalopathy,not provided",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:3 B:2",
      "phenotype_combined": "not provided|Developmental and epileptic encephalopathy, 36",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}