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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: 3-37050500-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=37050500&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 37050500,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000231790.8",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1682C>T",
          "hgvs_p": "p.Ala561Val",
          "transcript": "ENST00000413740.2",
          "protein_id": "ENSP00000416476.2",
          "transcript_support_level": 1,
          "aa_start": 561,
          "aa_end": null,
          "aa_length": 610,
          "cds_start": 1682,
          "cds_end": null,
          "cds_length": 1835,
          "cdna_start": 1873,
          "cdna_end": null,
          "cdna_length": 2219,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2118C>T",
          "hgvs_p": "p.Gly706Gly",
          "transcript": "NM_000249.4",
          "protein_id": "NP_000240.1",
          "transcript_support_level": null,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2118,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2148,
          "cdna_end": null,
          "cdna_length": 2494,
          "mane_select": "ENST00000231790.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2118C>T",
          "hgvs_p": "p.Gly706Gly",
          "transcript": "ENST00000231790.8",
          "protein_id": "ENSP00000231790.3",
          "transcript_support_level": 1,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2118,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 2148,
          "cdna_end": null,
          "cdna_length": 2494,
          "mane_select": "NM_000249.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1911C>T",
          "hgvs_p": "p.Gly637Gly",
          "transcript": "ENST00000456676.7",
          "protein_id": "ENSP00000416687.3",
          "transcript_support_level": 1,
          "aa_start": 637,
          "aa_end": null,
          "aa_length": 687,
          "cds_start": 1911,
          "cds_end": null,
          "cds_length": 2064,
          "cdna_start": 1941,
          "cdna_end": null,
          "cdna_length": 2285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1395C>T",
          "hgvs_p": "p.Gly465Gly",
          "transcript": "ENST00000458205.6",
          "protein_id": "ENSP00000402667.2",
          "transcript_support_level": 1,
          "aa_start": 465,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": 1395,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": 2262,
          "cdna_end": null,
          "cdna_length": 2608,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1950C>T",
          "hgvs_p": null,
          "transcript": "ENST00000432299.6",
          "protein_id": "ENSP00000416783.1",
          "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": 2444,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1229C>T",
          "hgvs_p": null,
          "transcript": "ENST00000447829.6",
          "protein_id": "ENSP00000399329.2",
          "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": 2247,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1019C>T",
          "hgvs_p": null,
          "transcript": "ENST00000458009.7",
          "protein_id": "ENSP00000411066.2",
          "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": 2340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.*10C>T",
          "hgvs_p": null,
          "transcript": "ENST00000450420.6",
          "protein_id": "ENSP00000393006.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 520,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1563,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1640,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1950C>T",
          "hgvs_p": null,
          "transcript": "ENST00000432299.6",
          "protein_id": "ENSP00000416783.1",
          "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": 2444,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1229C>T",
          "hgvs_p": null,
          "transcript": "ENST00000447829.6",
          "protein_id": "ENSP00000399329.2",
          "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": 2247,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "n.*1019C>T",
          "hgvs_p": null,
          "transcript": "ENST00000458009.7",
          "protein_id": "ENSP00000411066.2",
          "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": 2340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2025C>T",
          "hgvs_p": "p.Gly675Gly",
          "transcript": "NM_001354628.2",
          "protein_id": "NP_001341557.1",
          "transcript_support_level": null,
          "aa_start": 675,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2025,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2055,
          "cdna_end": null,
          "cdna_length": 2401,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2025C>T",
          "hgvs_p": "p.Gly675Gly",
          "transcript": "ENST00000616768.6",
          "protein_id": "ENSP00000480669.3",
          "transcript_support_level": 2,
          "aa_start": 675,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2025,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2101,
          "cdna_end": null,
          "cdna_length": 2447,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2019C>T",
          "hgvs_p": "p.Gly673Gly",
          "transcript": "NM_001354629.2",
          "protein_id": "NP_001341558.1",
          "transcript_support_level": null,
          "aa_start": 673,
          "aa_end": null,
          "aa_length": 723,
          "cds_start": 2019,
          "cds_end": null,
          "cds_length": 2172,
          "cdna_start": 2049,
          "cdna_end": null,
          "cdna_length": 2395,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.2019C>T",
          "hgvs_p": "p.Gly673Gly",
          "transcript": "ENST00000713802.1",
          "protein_id": "ENSP00000519108.1",
          "transcript_support_level": null,
          "aa_start": 673,
          "aa_end": null,
          "aa_length": 723,
          "cds_start": 2019,
          "cds_end": null,
          "cds_length": 2172,
          "cdna_start": 2025,
          "cdna_end": null,
          "cdna_length": 2366,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1953C>T",
          "hgvs_p": "p.Gly651Gly",
          "transcript": "NM_001354630.2",
          "protein_id": "NP_001341559.1",
          "transcript_support_level": null,
          "aa_start": 651,
          "aa_end": null,
          "aa_length": 701,
          "cds_start": 1953,
          "cds_end": null,
          "cds_length": 2106,
          "cdna_start": 1983,
          "cdna_end": null,
          "cdna_length": 2329,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1953C>T",
          "hgvs_p": "p.Gly651Gly",
          "transcript": "ENST00000673673.2",
          "protein_id": "ENSP00000500979.2",
          "transcript_support_level": null,
          "aa_start": 651,
          "aa_end": null,
          "aa_length": 701,
          "cds_start": 1953,
          "cds_end": null,
          "cds_length": 2106,
          "cdna_start": 2275,
          "cdna_end": null,
          "cdna_length": 2574,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1911C>T",
          "hgvs_p": "p.Gly637Gly",
          "transcript": "NM_001258271.2",
          "protein_id": "NP_001245200.1",
          "transcript_support_level": null,
          "aa_start": 637,
          "aa_end": null,
          "aa_length": 687,
          "cds_start": 1911,
          "cds_end": null,
          "cds_length": 2064,
          "cdna_start": 1941,
          "cdna_end": null,
          "cdna_length": 2287,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1824C>T",
          "hgvs_p": "p.Gly608Gly",
          "transcript": "NM_001167617.3",
          "protein_id": "NP_001161089.1",
          "transcript_support_level": null,
          "aa_start": 608,
          "aa_end": null,
          "aa_length": 658,
          "cds_start": 1824,
          "cds_end": null,
          "cds_length": 1977,
          "cdna_start": 2370,
          "cdna_end": null,
          "cdna_length": 2716,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH1",
          "gene_hgnc_id": 7127,
          "hgvs_c": "c.1824C>T",
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      ],
      "gene_symbol": "MLH1",
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      "dbsnp": "rs1800147",
      "frequency_reference_population": 0.0000013681631,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": 0.00000136816,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.140941321849823,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.188,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.1596,
      "alphamissense_prediction": "Benign",
      "bayesdelnoaf_score": 0.13,
      "bayesdelnoaf_prediction": "Uncertain_significance",
      "phylop100way_score": -0.711,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "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": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 3,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000231790.8",
          "gene_symbol": "MLH1",
          "hgnc_id": 7127,
          "effects": [
            "synonymous_variant"
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          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.2118C>T",
          "hgvs_p": "p.Gly706Gly"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}