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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: 22-50145772-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=50145772&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "22",
      "pos": 50145772,
      "ref": "A",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000262794.10",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "NM_018995.3",
          "protein_id": "NP_061868.1",
          "transcript_support_level": null,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1211,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3636,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 3957,
          "mane_select": "ENST00000262794.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "ENST00000262794.10",
          "protein_id": "ENSP00000262794.5",
          "transcript_support_level": 1,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1211,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3636,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 3957,
          "mane_select": "NM_018995.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "ENST00000395858.7",
          "protein_id": "ENSP00000379199.3",
          "transcript_support_level": 1,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 2613,
          "cdna_end": null,
          "cdna_length": 3763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "NM_001164104.2",
          "protein_id": "NP_001157576.1",
          "transcript_support_level": null,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 3819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2529A>C",
          "hgvs_p": "p.Thr843Thr",
          "transcript": "NM_001164105.2",
          "protein_id": "NP_001157577.1",
          "transcript_support_level": null,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 2999,
          "cdna_end": null,
          "cdna_length": 4192,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2529A>C",
          "hgvs_p": "p.Thr843Thr",
          "transcript": "ENST00000540615.5",
          "protein_id": "ENSP00000438542.1",
          "transcript_support_level": 2,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1165,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3498,
          "cdna_start": 2749,
          "cdna_end": null,
          "cdna_length": 3941,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "XM_011530696.2",
          "protein_id": "XP_011528998.1",
          "transcript_support_level": null,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 4092,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2529A>C",
          "hgvs_p": "p.Thr843Thr",
          "transcript": "XM_011530697.2",
          "protein_id": "XP_011528999.1",
          "transcript_support_level": null,
          "aa_start": 843,
          "aa_end": null,
          "aa_length": 1236,
          "cds_start": 2529,
          "cds_end": null,
          "cds_length": 3711,
          "cdna_start": 2999,
          "cdna_end": null,
          "cdna_length": 4419,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "XM_017028833.2",
          "protein_id": "XP_016884322.1",
          "transcript_support_level": null,
          "aa_start": 863,
          "aa_end": null,
          "aa_length": 1210,
          "cds_start": 2589,
          "cds_end": null,
          "cds_length": 3633,
          "cdna_start": 2672,
          "cdna_end": null,
          "cdna_length": 3954,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2448A>C",
          "hgvs_p": "p.Thr816Thr",
          "transcript": "XM_011530698.2",
          "protein_id": "XP_011529000.1",
          "transcript_support_level": null,
          "aa_start": 816,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": 2448,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": 2531,
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          "cdna_length": 3951,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2433A>C",
          "hgvs_p": "p.Thr811Thr",
          "transcript": "XM_011530699.2",
          "protein_id": "XP_011529001.1",
          "transcript_support_level": null,
          "aa_start": 811,
          "aa_end": null,
          "aa_length": 1204,
          "cds_start": 2433,
          "cds_end": null,
          "cds_length": 3615,
          "cdna_start": 2643,
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          "cdna_length": 4063,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2433A>C",
          "hgvs_p": "p.Thr811Thr",
          "transcript": "XM_011530700.3",
          "protein_id": "XP_011529002.1",
          "transcript_support_level": null,
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          "cds_start": 2433,
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          "cdna_start": 3017,
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          "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": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
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          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2529A>C",
          "hgvs_p": "p.Thr843Thr",
          "transcript": "XM_005261923.5",
          "protein_id": "XP_005261980.1",
          "transcript_support_level": null,
          "aa_start": 843,
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          "cds_start": 2529,
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          "cdna_start": 2999,
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          "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": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "XM_011530701.1",
          "protein_id": "XP_011529003.1",
          "transcript_support_level": null,
          "aa_start": 863,
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          "cds_start": 2589,
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          "cdna_start": 2672,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
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          "protein_coding": true,
          "strand": true,
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          ],
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          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.1866A>C",
          "hgvs_p": "p.Thr622Thr",
          "transcript": "XM_047441413.1",
          "protein_id": "XP_047297369.1",
          "transcript_support_level": null,
          "aa_start": 622,
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          "cds_start": 1866,
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          "cdna_length": 3380,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr",
          "transcript": "XM_047441414.1",
          "protein_id": "XP_047297370.1",
          "transcript_support_level": null,
          "aa_start": 863,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.1011A>C",
          "hgvs_p": "p.Thr337Thr",
          "transcript": "XM_017028835.2",
          "protein_id": "XP_016884324.1",
          "transcript_support_level": null,
          "aa_start": 337,
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          "aa_length": 730,
          "cds_start": 1011,
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          "cds_length": 2193,
          "cdna_start": 1087,
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          "cdna_length": 2507,
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        },
        {
          "aa_ref": "T",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.1011A>C",
          "hgvs_p": "p.Thr337Thr",
          "transcript": "XM_017028836.2",
          "protein_id": "XP_016884325.1",
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          "cdna_start": 1041,
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          "cdna_length": 2461,
          "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": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "MOV10L1",
          "gene_hgnc_id": 7201,
          "hgvs_c": "c.1011A>C",
          "hgvs_p": "p.Thr337Thr",
          "transcript": "XM_047441415.1",
          "protein_id": "XP_047297371.1",
          "transcript_support_level": null,
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          "cds_start": 1011,
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          "cdna_start": 1110,
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          "cdna_length": 2530,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MOV10L1",
      "gene_hgnc_id": 7201,
      "dbsnp": "rs2272838",
      "frequency_reference_population": 0.24499893,
      "hom_count_reference_population": 50202,
      "allele_count_reference_population": 395368,
      "gnomad_exomes_af": 0.246814,
      "gnomad_genomes_af": 0.227563,
      "gnomad_exomes_ac": 360747,
      "gnomad_genomes_ac": 34621,
      "gnomad_exomes_homalt": 45883,
      "gnomad_genomes_homalt": 4319,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -1.0299999713897705,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -1.03,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -2.724,
      "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": -13,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -13,
          "benign_score": 13,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000262794.10",
          "gene_symbol": "MOV10L1",
          "hgnc_id": 7201,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2589A>C",
          "hgvs_p": "p.Thr863Thr"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}