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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-20167752-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=20167752&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 20167752,
      "ref": "A",
      "alt": "G",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "ENST00000379565.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1444-5T>C",
          "hgvs_p": null,
          "transcript": "NM_004586.3",
          "protein_id": "NP_004577.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7987,
          "mane_select": "ENST00000379565.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1444-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000379565.9",
          "protein_id": "ENSP00000368884.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7987,
          "mane_select": "NM_004586.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "NM_001438340.1",
          "protein_id": "NP_001425269.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000642835.1",
          "protein_id": "ENSP00000494769.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2841,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000643085.1",
          "protein_id": "ENSP00000496271.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4064,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000643337.1",
          "protein_id": "ENSP00000493487.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3054,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000643402.1",
          "protein_id": "ENSP00000493862.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3294,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000644368.1",
          "protein_id": "ENSP00000495776.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2991,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000645270.1",
          "protein_id": "ENSP00000494967.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3961,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000646610.1",
          "protein_id": "ENSP00000495462.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2682,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1360-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647265.1",
          "protein_id": "ENSP00000494220.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 712,
          "cds_start": -4,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
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          "hgvs_c": "c.1357-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000457145.6",
          "protein_id": "ENSP00000407655.2",
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          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2820,
          "mane_select": null,
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        },
        {
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          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 24,
          "intron_rank": 18,
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          "gene_symbol": "RPS6KA3",
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          "hgvs_c": "c.1357-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000644893.1",
          "protein_id": "ENSP00000495974.1",
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          "cdna_length": 2451,
          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.208-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000479809.1",
          "protein_id": "ENSP00000494866.1",
          "transcript_support_level": 5,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "intron_rank": 12,
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          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*816-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000643073.1",
          "protein_id": "ENSP00000495839.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 2393,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*665-5T>C",
          "hgvs_p": null,
          "transcript": "ENST00000645268.1",
          "protein_id": "ENSP00000496226.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
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          "cds_length": null,
          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1462-5T>C",
          "hgvs_p": null,
          "transcript": "XM_011545555.2",
          "protein_id": "XP_011543857.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 746,
          "cds_start": -4,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1459-5T>C",
          "hgvs_p": null,
          "transcript": "XM_011545556.2",
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          "cdna_start": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "consequences": [
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          "exon_count": 23,
          "intron_rank": 16,
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          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1444-5T>C",
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          "transcript": "XM_047442332.1",
          "protein_id": "XP_047298288.1",
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          "cdna_start": null,
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          "cdna_length": 3926,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.1441-5T>C",
          "hgvs_p": null,
          "transcript": "XM_005274573.3",
          "protein_id": "XP_005274630.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 739,
          "cds_start": -4,
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          "cds_length": 2220,
          "cdna_start": null,
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          "cdna_length": 7984,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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      ],
      "gene_symbol": "RPS6KA3",
      "gene_hgnc_id": 10432,
      "dbsnp": "rs781136878",
      "frequency_reference_population": 0.000011462041,
      "hom_count_reference_population": 6,
      "allele_count_reference_population": 12,
      "gnomad_exomes_af": 0.00000963523,
      "gnomad_genomes_af": 0.0000265811,
      "gnomad_exomes_ac": 9,
      "gnomad_genomes_ac": 3,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.27000001072883606,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.4000000059604645,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.27,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 3.327,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.277151528933077,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -14,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BS2",
      "acmg_by_gene": [
        {
          "score": -14,
          "benign_score": 14,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Very_Strong",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000379565.9",
          "gene_symbol": "RPS6KA3",
          "hgnc_id": 10432,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AD,XL",
          "hgvs_c": "c.1444-5T>C",
          "hgvs_p": null
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      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}