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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: 5-132393688-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=132393688&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 132393688,
      "ref": "G",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000245407.8",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Arg488His",
          "transcript": "NM_003060.4",
          "protein_id": "NP_003051.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 557,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 1674,
          "cdna_start": 1726,
          "cdna_end": null,
          "cdna_length": 3277,
          "mane_select": "ENST00000245407.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Arg488His",
          "transcript": "ENST00000245407.8",
          "protein_id": "ENSP00000245407.3",
          "transcript_support_level": 1,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 557,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 1674,
          "cdna_start": 1726,
          "cdna_end": null,
          "cdna_length": 3277,
          "mane_select": "NM_003060.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1535G>A",
          "hgvs_p": "p.Arg512His",
          "transcript": "ENST00000435065.7",
          "protein_id": "ENSP00000402760.2",
          "transcript_support_level": 1,
          "aa_start": 512,
          "aa_end": null,
          "aa_length": 581,
          "cds_start": 1535,
          "cds_end": null,
          "cds_length": 1746,
          "cdna_start": 1691,
          "cdna_end": null,
          "cdna_length": 2825,
          "mane_select": null,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.*315G>A",
          "hgvs_p": null,
          "transcript": "ENST00000448810.6",
          "protein_id": "ENSP00000401860.2",
          "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": 2656,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.*315G>A",
          "hgvs_p": null,
          "transcript": "ENST00000448810.6",
          "protein_id": "ENSP00000401860.2",
          "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": 2656,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1535G>A",
          "hgvs_p": "p.Arg512His",
          "transcript": "NM_001308122.2",
          "protein_id": "NP_001295051.1",
          "transcript_support_level": null,
          "aa_start": 512,
          "aa_end": null,
          "aa_length": 581,
          "cds_start": 1535,
          "cds_end": null,
          "cds_length": 1746,
          "cdna_start": 1798,
          "cdna_end": null,
          "cdna_length": 3349,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1511G>A",
          "hgvs_p": "p.Arg504His",
          "transcript": "ENST00000693308.1",
          "protein_id": "ENSP00000509770.1",
          "transcript_support_level": null,
          "aa_start": 504,
          "aa_end": null,
          "aa_length": 573,
          "cds_start": 1511,
          "cds_end": null,
          "cds_length": 1722,
          "cdna_start": 1645,
          "cdna_end": null,
          "cdna_length": 3146,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1445G>A",
          "hgvs_p": "p.Arg482His",
          "transcript": "ENST00000692413.1",
          "protein_id": "ENSP00000509374.1",
          "transcript_support_level": null,
          "aa_start": 482,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": 1445,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": 1579,
          "cdna_end": null,
          "cdna_length": 3080,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.1310G>A",
          "hgvs_p": "p.Arg437His",
          "transcript": "ENST00000689271.1",
          "protein_id": "ENSP00000510797.1",
          "transcript_support_level": null,
          "aa_start": 437,
          "aa_end": null,
          "aa_length": 506,
          "cds_start": 1310,
          "cds_end": null,
          "cds_length": 1521,
          "cdna_start": 1444,
          "cdna_end": null,
          "cdna_length": 2945,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.935G>A",
          "hgvs_p": "p.Arg312His",
          "transcript": "XM_017009778.3",
          "protein_id": "XP_016865267.1",
          "transcript_support_level": null,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": 935,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": 1622,
          "cdna_end": null,
          "cdna_length": 3173,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.851G>A",
          "hgvs_p": "p.Arg284His",
          "transcript": "XM_047417596.1",
          "protein_id": "XP_047273552.1",
          "transcript_support_level": null,
          "aa_start": 284,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": 851,
          "cds_end": null,
          "cds_length": 1062,
          "cdna_start": 6647,
          "cdna_end": null,
          "cdna_length": 8198,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "c.845G>A",
          "hgvs_p": "p.Arg282His",
          "transcript": "XM_011543590.3",
          "protein_id": "XP_011541892.1",
          "transcript_support_level": null,
          "aa_start": 282,
          "aa_end": null,
          "aa_length": 351,
          "cds_start": 845,
          "cds_end": null,
          "cds_length": 1056,
          "cdna_start": 944,
          "cdna_end": null,
          "cdna_length": 2495,
          "mane_select": null,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.*195G>A",
          "hgvs_p": null,
          "transcript": "ENST00000447841.5",
          "protein_id": "ENSP00000389284.1",
          "transcript_support_level": 3,
          "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": 998,
          "mane_select": null,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.8885G>A",
          "hgvs_p": null,
          "transcript": "ENST00000461013.5",
          "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": 10435,
          "mane_select": null,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.2141G>A",
          "hgvs_p": null,
          "transcript": "ENST00000475308.1",
          "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": 3693,
          "mane_select": null,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.1604G>A",
          "hgvs_p": null,
          "transcript": "ENST00000685543.1",
          "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": 2749,
          "mane_select": null,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.*627G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686757.1",
          "protein_id": "ENSP00000510721.1",
          "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": 3117,
          "mane_select": null,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.455G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686868.1",
          "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": 1956,
          "mane_select": null,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.4148G>A",
          "hgvs_p": null,
          "transcript": "ENST00000687740.1",
          "protein_id": null,
          "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,
          "cdna_end": null,
          "cdna_length": 5649,
          "mane_select": null,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.2773G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688151.1",
          "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": 4274,
          "mane_select": null,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC22A5",
          "gene_hgnc_id": 10969,
          "hgvs_c": "n.*627G>A",
          "hgvs_p": null,
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      ],
      "gene_symbol": "SLC22A5",
      "gene_hgnc_id": 10969,
      "dbsnp": "rs28383481",
      "frequency_reference_population": 0.0045560882,
      "hom_count_reference_population": 27,
      "allele_count_reference_population": 7354,
      "gnomad_exomes_af": 0.0046749,
      "gnomad_genomes_af": 0.00341535,
      "gnomad_exomes_ac": 6834,
      "gnomad_genomes_ac": 520,
      "gnomad_exomes_homalt": 26,
      "gnomad_genomes_homalt": 1,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.017382115125656128,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.376,
      "revel_prediction": "Uncertain_significance",
      "alphamissense_score": 0.141,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.09,
      "bayesdelnoaf_prediction": "Uncertain_significance",
      "phylop100way_score": 2.758,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "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": -7,
      "acmg_classification": "Benign",
      "acmg_criteria": "PM5,BP4_Strong,BS1_Supporting,BS2",
      "acmg_by_gene": [
        {
          "score": -7,
          "benign_score": 9,
          "pathogenic_score": 2,
          "criteria": [
            "PM5",
            "BP4_Strong",
            "BS1_Supporting",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000245407.8",
          "gene_symbol": "SLC22A5",
          "hgnc_id": 10969,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Arg488His"
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      ],
      "clinvar_disease": "Renal carnitine transport defect,not provided,not specified",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "P:3 LP:2 US:9 LB:3 B:1",
      "phenotype_combined": "not provided|Renal carnitine transport defect|not specified",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}