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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-71141289-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=71141289&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 71141289,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000374080.8",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6327G>A",
          "hgvs_p": "p.Gln2109Gln",
          "transcript": "NM_005120.3",
          "protein_id": "NP_005111.2",
          "transcript_support_level": null,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6486,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "ENST00000374080.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6327G>A",
          "hgvs_p": "p.Gln2109Gln",
          "transcript": "ENST00000374080.8",
          "protein_id": "ENSP00000363193.3",
          "transcript_support_level": 1,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6486,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "NM_005120.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6336G>A",
          "hgvs_p": "p.Gln2112Gln",
          "transcript": "ENST00000374102.6",
          "protein_id": "ENSP00000363215.2",
          "transcript_support_level": 1,
          "aa_start": 2112,
          "aa_end": null,
          "aa_length": 2180,
          "cds_start": 6336,
          "cds_end": null,
          "cds_length": 6543,
          "cdna_start": 6462,
          "cdna_end": null,
          "cdna_length": 6901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6333G>A",
          "hgvs_p": "p.Gln2111Gln",
          "transcript": "ENST00000690145.1",
          "protein_id": "ENSP00000508818.1",
          "transcript_support_level": null,
          "aa_start": 2111,
          "aa_end": null,
          "aa_length": 2179,
          "cds_start": 6333,
          "cds_end": null,
          "cds_length": 6540,
          "cdna_start": 6363,
          "cdna_end": null,
          "cdna_length": 6739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6324G>A",
          "hgvs_p": "p.Gln2108Gln",
          "transcript": "ENST00000692304.1",
          "protein_id": "ENSP00000508427.1",
          "transcript_support_level": null,
          "aa_start": 2108,
          "aa_end": null,
          "aa_length": 2176,
          "cds_start": 6324,
          "cds_end": null,
          "cds_length": 6531,
          "cdna_start": 6536,
          "cdna_end": null,
          "cdna_length": 8628,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6261G>A",
          "hgvs_p": "p.Gln2087Gln",
          "transcript": "ENST00000690242.1",
          "protein_id": "ENSP00000510090.1",
          "transcript_support_level": null,
          "aa_start": 2087,
          "aa_end": null,
          "aa_length": 2155,
          "cds_start": 6261,
          "cds_end": null,
          "cds_length": 6468,
          "cdna_start": 6473,
          "cdna_end": null,
          "cdna_length": 6912,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6252G>A",
          "hgvs_p": "p.Gln2084Gln",
          "transcript": "ENST00000687382.1",
          "protein_id": "ENSP00000510724.1",
          "transcript_support_level": null,
          "aa_start": 2084,
          "aa_end": null,
          "aa_length": 2152,
          "cds_start": 6252,
          "cds_end": null,
          "cds_length": 6459,
          "cdna_start": 6451,
          "cdna_end": null,
          "cdna_length": 6764,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6207G>A",
          "hgvs_p": "p.Gln2069Gln",
          "transcript": "ENST00000333646.11",
          "protein_id": "ENSP00000333125.8",
          "transcript_support_level": 5,
          "aa_start": 2069,
          "aa_end": null,
          "aa_length": 2137,
          "cds_start": 6207,
          "cds_end": null,
          "cds_length": 6414,
          "cdna_start": 6366,
          "cdna_end": null,
          "cdna_length": 6797,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.4278G>A",
          "hgvs_p": "p.Gln1426Gln",
          "transcript": "ENST00000693391.1",
          "protein_id": "ENSP00000509563.1",
          "transcript_support_level": null,
          "aa_start": 1426,
          "aa_end": null,
          "aa_length": 1494,
          "cds_start": 4278,
          "cds_end": null,
          "cds_length": 4485,
          "cdna_start": 4278,
          "cdna_end": null,
          "cdna_length": 4699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.1299G>A",
          "hgvs_p": "p.Gln433Gln",
          "transcript": "ENST00000444034.2",
          "protein_id": "ENSP00000404373.2",
          "transcript_support_level": 5,
          "aa_start": 433,
          "aa_end": null,
          "aa_length": 501,
          "cds_start": 1299,
          "cds_end": null,
          "cds_length": 1506,
          "cdna_start": 1299,
          "cdna_end": null,
          "cdna_length": 1675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.369G>A",
          "hgvs_p": "p.Gln123Gln",
          "transcript": "ENST00000688231.1",
          "protein_id": "ENSP00000508591.1",
          "transcript_support_level": null,
          "aa_start": 123,
          "aa_end": null,
          "aa_length": 246,
          "cds_start": 369,
          "cds_end": null,
          "cds_length": 741,
          "cdna_start": 371,
          "cdna_end": null,
          "cdna_length": 854,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3025G>A",
          "hgvs_p": null,
          "transcript": "ENST00000685182.1",
          "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": 3446,
          "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": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.2713G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686169.1",
          "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": 3148,
          "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": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.*6232G>A",
          "hgvs_p": null,
          "transcript": "ENST00000686548.1",
          "protein_id": "ENSP00000509582.1",
          "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": 6852,
          "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": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3042G>A",
          "hgvs_p": null,
          "transcript": "ENST00000687161.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 3481,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3086G>A",
          "hgvs_p": null,
          "transcript": "ENST00000687701.1",
          "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": 3499,
          "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": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.1000G>A",
          "hgvs_p": null,
          "transcript": "ENST00000687973.1",
          "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": 1423,
          "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": 25,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.4322G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688079.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 4676,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.1887G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688508.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2263,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.*178G>A",
          "hgvs_p": null,
          "transcript": "ENST00000688774.1",
          "protein_id": "ENSP00000508823.1",
          "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": 1186,
          "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": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.646G>A",
          "hgvs_p": null,
          "transcript": "ENST00000689489.1",
          "protein_id": null,
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      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.49000000953674316,
      "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": -0.49,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.038,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000374080.8",
          "gene_symbol": "MED12",
          "hgnc_id": 11957,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.6327G>A",
          "hgvs_p": "p.Gln2109Gln"
        },
        {
          "score": -4,
          "benign_score": 6,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000740246.1",
          "gene_symbol": "ENSG00000228427",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.347-438C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "FG syndrome",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "FG syndrome",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}