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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: 15-44573601-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=44573601&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 44573601,
      "ref": "C",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000261866.12",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6151G>T",
          "hgvs_p": "p.Glu2051*",
          "transcript": "NM_025137.4",
          "protein_id": "NP_079413.3",
          "transcript_support_level": null,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2443,
          "cds_start": 6151,
          "cds_end": null,
          "cds_length": 7332,
          "cdna_start": 6166,
          "cdna_end": null,
          "cdna_length": 7772,
          "mane_select": "ENST00000261866.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6151G>T",
          "hgvs_p": "p.Glu2051*",
          "transcript": "ENST00000261866.12",
          "protein_id": "ENSP00000261866.7",
          "transcript_support_level": 1,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2443,
          "cds_start": 6151,
          "cds_end": null,
          "cds_length": 7332,
          "cdna_start": 6166,
          "cdna_end": null,
          "cdna_length": 7772,
          "mane_select": "NM_025137.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6151G>T",
          "hgvs_p": "p.Glu2051*",
          "transcript": "ENST00000427534.6",
          "protein_id": "ENSP00000396110.2",
          "transcript_support_level": 1,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2265,
          "cds_start": 6151,
          "cds_end": null,
          "cds_length": 6798,
          "cdna_start": 6151,
          "cdna_end": null,
          "cdna_length": 6935,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.516G>T",
          "hgvs_p": null,
          "transcript": "ENST00000558080.1",
          "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": 759,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": 30,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.5867-781G>T",
          "hgvs_p": null,
          "transcript": "ENST00000535302.6",
          "protein_id": "ENSP00000445278.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2330,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6993,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7288,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6007G>T",
          "hgvs_p": "p.Glu2003*",
          "transcript": "NM_001411132.1",
          "protein_id": "NP_001398061.1",
          "transcript_support_level": null,
          "aa_start": 2003,
          "aa_end": null,
          "aa_length": 2395,
          "cds_start": 6007,
          "cds_end": null,
          "cds_length": 7188,
          "cdna_start": 6022,
          "cdna_end": null,
          "cdna_length": 7628,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6007G>T",
          "hgvs_p": "p.Glu2003*",
          "transcript": "ENST00000682065.1",
          "protein_id": "ENSP00000507025.1",
          "transcript_support_level": null,
          "aa_start": 2003,
          "aa_end": null,
          "aa_length": 2395,
          "cds_start": 6007,
          "cds_end": null,
          "cds_length": 7188,
          "cdna_start": 6038,
          "cdna_end": null,
          "cdna_length": 7624,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6151G>T",
          "hgvs_p": "p.Glu2051*",
          "transcript": "ENST00000684235.1",
          "protein_id": "ENSP00000508295.1",
          "transcript_support_level": null,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2392,
          "cds_start": 6151,
          "cds_end": null,
          "cds_length": 7179,
          "cdna_start": 6182,
          "cdna_end": null,
          "cdna_length": 7574,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.5950G>T",
          "hgvs_p": "p.Glu1984*",
          "transcript": "ENST00000682669.1",
          "protein_id": "ENSP00000507782.1",
          "transcript_support_level": null,
          "aa_start": 1984,
          "aa_end": null,
          "aa_length": 2376,
          "cds_start": 5950,
          "cds_end": null,
          "cds_length": 7131,
          "cdna_start": 5981,
          "cdna_end": null,
          "cdna_length": 7567,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.6151G>T",
          "hgvs_p": "p.Glu2051*",
          "transcript": "ENST00000558319.5",
          "protein_id": "ENSP00000453599.1",
          "transcript_support_level": 5,
          "aa_start": 2051,
          "aa_end": null,
          "aa_length": 2079,
          "cds_start": 6151,
          "cds_end": null,
          "cds_length": 6240,
          "cdna_start": 6182,
          "cdna_end": null,
          "cdna_length": 6426,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.5548G>T",
          "hgvs_p": "p.Glu1850*",
          "transcript": "XM_047433144.1",
          "protein_id": "XP_047289100.1",
          "transcript_support_level": null,
          "aa_start": 1850,
          "aa_end": null,
          "aa_length": 2242,
          "cds_start": 5548,
          "cds_end": null,
          "cds_length": 6729,
          "cdna_start": 6412,
          "cdna_end": null,
          "cdna_length": 8018,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "c.3028G>T",
          "hgvs_p": "p.Glu1010*",
          "transcript": "XM_047433146.1",
          "protein_id": "XP_047289102.1",
          "transcript_support_level": null,
          "aa_start": 1010,
          "aa_end": null,
          "aa_length": 1402,
          "cds_start": 3028,
          "cds_end": null,
          "cds_length": 4209,
          "cdna_start": 3132,
          "cdna_end": null,
          "cdna_length": 4738,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.220G>T",
          "hgvs_p": null,
          "transcript": "ENST00000559933.1",
          "protein_id": null,
          "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": 518,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.83G>T",
          "hgvs_p": null,
          "transcript": "ENST00000561268.5",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": 530,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.2379G>T",
          "hgvs_p": null,
          "transcript": "ENST00000561391.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2861,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.*2408G>T",
          "hgvs_p": null,
          "transcript": "ENST00000682460.1",
          "protein_id": "ENSP00000508334.1",
          "transcript_support_level": null,
          "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": 7691,
          "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": 33,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.*2643G>T",
          "hgvs_p": null,
          "transcript": "ENST00000682495.1",
          "protein_id": "ENSP00000507166.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 7893,
          "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": 30,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.*2914G>T",
          "hgvs_p": null,
          "transcript": "ENST00000683186.1",
          "protein_id": "ENSP00000507268.1",
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 7578,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.*101G>T",
          "hgvs_p": null,
          "transcript": "ENST00000683734.1",
          "protein_id": "ENSP00000508319.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 7612,
          "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": 27,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.5197G>T",
          "hgvs_p": null,
          "transcript": "ENST00000683753.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 6783,
          "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": 32,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SPG11",
          "gene_hgnc_id": 11226,
          "hgvs_c": "n.*2571G>T",
          "hgvs_p": null,
          "transcript": "ENST00000684038.1",
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      "gene_symbol": "SPG11",
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      "dbsnp": "rs771057519",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
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      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": 0.5299999713897705,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": 0.53,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 1.272,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "acmg_score": 12,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
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          "benign_score": 0,
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            "PP5_Moderate"
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          "verdict": "Pathogenic",
          "transcript": "ENST00000261866.12",
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          "effects": [
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          "inheritance_mode": "AR",
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      ],
      "clinvar_disease": "Hereditary spastic paraplegia 11",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LP:1",
      "phenotype_combined": "Hereditary spastic paraplegia 11",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}