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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: 8-67149784-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=67149784&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 67149784,
      "ref": "T",
      "alt": "C",
      "effect": "splice_region_variant,synonymous_variant",
      "transcript": "ENST00000678616.1",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1977T>C",
          "hgvs_p": "p.Thr659Thr",
          "transcript": "NM_001382391.1",
          "protein_id": "NP_001369320.1",
          "transcript_support_level": null,
          "aa_start": 659,
          "aa_end": null,
          "aa_length": 1226,
          "cds_start": 1977,
          "cds_end": null,
          "cds_length": 3681,
          "cdna_start": 2134,
          "cdna_end": null,
          "cdna_length": 4859,
          "mane_select": "ENST00000678616.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1977T>C",
          "hgvs_p": "p.Thr659Thr",
          "transcript": "ENST00000678616.1",
          "protein_id": "ENSP00000504733.1",
          "transcript_support_level": null,
          "aa_start": 659,
          "aa_end": null,
          "aa_length": 1226,
          "cds_start": 1977,
          "cds_end": null,
          "cds_length": 3681,
          "cdna_start": 2134,
          "cdna_end": null,
          "cdna_length": 4859,
          "mane_select": "NM_001382391.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.2043T>C",
          "hgvs_p": "p.Thr681Thr",
          "transcript": "ENST00000262210.11",
          "protein_id": "ENSP00000262210.6",
          "transcript_support_level": 1,
          "aa_start": 681,
          "aa_end": null,
          "aa_length": 1248,
          "cds_start": 2043,
          "cds_end": null,
          "cds_length": 3747,
          "cdna_start": 2102,
          "cdna_end": null,
          "cdna_length": 4476,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1079-4240T>C",
          "hgvs_p": null,
          "transcript": "ENST00000519668.1",
          "protein_id": "ENSP00000430092.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3715,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.2085T>C",
          "hgvs_p": "p.Thr695Thr",
          "transcript": "ENST00000676605.1",
          "protein_id": "ENSP00000503605.1",
          "transcript_support_level": null,
          "aa_start": 695,
          "aa_end": null,
          "aa_length": 1262,
          "cds_start": 2085,
          "cds_end": null,
          "cds_length": 3789,
          "cdna_start": 2122,
          "cdna_end": null,
          "cdna_length": 5011,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.2085T>C",
          "hgvs_p": "p.Thr695Thr",
          "transcript": "ENST00000678542.1",
          "protein_id": "ENSP00000503878.1",
          "transcript_support_level": null,
          "aa_start": 695,
          "aa_end": null,
          "aa_length": 1262,
          "cds_start": 2085,
          "cds_end": null,
          "cds_length": 3789,
          "cdna_start": 2122,
          "cdna_end": null,
          "cdna_length": 5011,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.2067T>C",
          "hgvs_p": "p.Thr689Thr",
          "transcript": "ENST00000674993.1",
          "protein_id": "ENSP00000502454.1",
          "transcript_support_level": null,
          "aa_start": 689,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": 2067,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": 2098,
          "cdna_end": null,
          "cdna_length": 3802,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.2043T>C",
          "hgvs_p": "p.Thr681Thr",
          "transcript": "NM_001364869.1",
          "protein_id": "NP_001351798.1",
          "transcript_support_level": null,
          "aa_start": 681,
          "aa_end": null,
          "aa_length": 1248,
          "cds_start": 2043,
          "cds_end": null,
          "cds_length": 3747,
          "cdna_start": 2050,
          "cdna_end": null,
          "cdna_length": 4775,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1962T>C",
          "hgvs_p": "p.Thr654Thr",
          "transcript": "NM_024790.7",
          "protein_id": "NP_079066.5",
          "transcript_support_level": null,
          "aa_start": 654,
          "aa_end": null,
          "aa_length": 1221,
          "cds_start": 1962,
          "cds_end": null,
          "cds_length": 3666,
          "cdna_start": 1969,
          "cdna_end": null,
          "cdna_length": 4694,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
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          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1962T>C",
          "hgvs_p": "p.Thr654Thr",
          "transcript": "ENST00000676317.1",
          "protein_id": "ENSP00000502047.1",
          "transcript_support_level": null,
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          "cds_start": 1962,
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          "cdna_start": 1993,
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          "mane_select": null,
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1956T>C",
          "hgvs_p": "p.Thr652Thr",
          "transcript": "ENST00000676847.1",
          "protein_id": "ENSP00000503336.1",
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          "cds_start": 1956,
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          "mane_select": null,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "CSPP1",
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          "transcript": "ENST00000677592.1",
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        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "hgvs_c": "c.1935T>C",
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          "transcript": "ENST00000676113.1",
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
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          "protein_coding": true,
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            "splice_region_variant",
            "synonymous_variant"
          ],
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          "gene_symbol": "CSPP1",
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          "hgvs_c": "c.1896T>C",
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        {
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          "gene_symbol": "CSPP1",
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        {
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          "protein_coding": true,
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          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "CSPP1",
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          "hgvs_c": "c.1863T>C",
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          "transcript": "NM_001364870.1",
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        {
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          "protein_coding": true,
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            "splice_region_variant",
            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "CSPP1",
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        {
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          "gene_symbol": "CSPP1",
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        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "CSPP1",
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          "hgvs_c": "c.1962T>C",
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          "transcript": "NM_001438331.1",
          "protein_id": "NP_001425260.1",
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          "cds_start": 1962,
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          "cdna_start": 1969,
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          "cdna_length": 4555,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1512T>C",
          "hgvs_p": "p.Thr504Thr",
          "transcript": "ENST00000678318.1",
          "protein_id": "ENSP00000503690.1",
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          "transcript": "XM_047422249.1",
          "protein_id": "XP_047278205.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cds_length": 3594,
          "cdna_start": null,
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          "cdna_length": 4646,
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        {
          "aa_ref": null,
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          "protein_coding": true,
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          "exon_count": 27,
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          "gene_symbol": "CSPP1",
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          "hgvs_c": "c.1862-4240T>C",
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          "transcript": "XM_047422255.1",
          "protein_id": "XP_047278211.1",
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        {
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          ],
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          "exon_count": 30,
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          "gene_symbol": "CSPP1",
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          "hgvs_c": "c.2108-4240T>C",
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          "transcript": "XM_047422257.1",
          "protein_id": "XP_047278213.1",
          "transcript_support_level": null,
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        {
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          "gene_symbol": "CSPP1",
          "gene_hgnc_id": 26193,
          "hgvs_c": "c.1511-4240T>C",
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          "transcript": "XM_047422260.1",
          "protein_id": "XP_047278216.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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      ],
      "gene_symbol": "CSPP1",
      "gene_hgnc_id": 26193,
      "dbsnp": "rs114177619",
      "frequency_reference_population": 0.0013648309,
      "hom_count_reference_population": 25,
      "allele_count_reference_population": 2094,
      "gnomad_exomes_af": 0.000659902,
      "gnomad_genomes_af": 0.00776446,
      "gnomad_exomes_ac": 912,
      "gnomad_genomes_ac": 1182,
      "gnomad_exomes_homalt": 12,
      "gnomad_genomes_homalt": 13,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.47999998927116394,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.07999999821186066,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.48,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.163,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.08,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.0013182197978119,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000678616.1",
          "gene_symbol": "CSPP1",
          "hgnc_id": 26193,
          "effects": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1977T>C",
          "hgvs_p": "p.Thr659Thr"
        }
      ],
      "clinvar_disease": "Joubert syndrome 21,not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:3",
      "phenotype_combined": "Joubert syndrome 21|not specified|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}