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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: 9-131512101-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=131512101&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 131512101,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000402686.8",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp",
          "transcript": "NM_001077365.2",
          "protein_id": "NP_001070833.1",
          "transcript_support_level": null,
          "aa_start": 349,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 1047,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 1233,
          "cdna_end": null,
          "cdna_length": 3057,
          "mane_select": "ENST00000402686.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp",
          "transcript": "ENST00000402686.8",
          "protein_id": "ENSP00000385797.4",
          "transcript_support_level": 1,
          "aa_start": 349,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 1047,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 1233,
          "cdna_end": null,
          "cdna_length": 3057,
          "mane_select": "NM_001077365.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1113T>C",
          "hgvs_p": "p.Asp371Asp",
          "transcript": "ENST00000372228.9",
          "protein_id": "ENSP00000361302.3",
          "transcript_support_level": 1,
          "aa_start": 371,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 1113,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 1428,
          "cdna_end": null,
          "cdna_length": 3252,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1104T>C",
          "hgvs_p": "p.Asp368Asp",
          "transcript": "ENST00000423007.6",
          "protein_id": "ENSP00000404119.2",
          "transcript_support_level": 1,
          "aa_start": 368,
          "aa_end": null,
          "aa_length": 744,
          "cds_start": 1104,
          "cds_end": null,
          "cds_length": 2235,
          "cdna_start": 1104,
          "cdna_end": null,
          "cdna_length": 2235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1113T>C",
          "hgvs_p": "p.Asp371Asp",
          "transcript": "NM_001353193.2",
          "protein_id": "NP_001340122.2",
          "transcript_support_level": null,
          "aa_start": 371,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 1113,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 1539,
          "cdna_end": null,
          "cdna_length": 3363,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1113T>C",
          "hgvs_p": "p.Asp371Asp",
          "transcript": "NM_007171.4",
          "protein_id": "NP_009102.4",
          "transcript_support_level": null,
          "aa_start": 371,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 1113,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 1299,
          "cdna_end": null,
          "cdna_length": 3123,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp",
          "transcript": "NM_001136113.2",
          "protein_id": "NP_001129585.1",
          "transcript_support_level": null,
          "aa_start": 349,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 1047,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 1473,
          "cdna_end": null,
          "cdna_length": 3297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp",
          "transcript": "ENST00000676640.1",
          "protein_id": "ENSP00000503281.1",
          "transcript_support_level": null,
          "aa_start": 349,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 1047,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 1485,
          "cdna_end": null,
          "cdna_length": 3309,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1035T>C",
          "hgvs_p": "p.Asp345Asp",
          "transcript": "NM_001374689.1",
          "protein_id": "NP_001361618.1",
          "transcript_support_level": null,
          "aa_start": 345,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 1035,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": 1231,
          "cdna_end": null,
          "cdna_length": 3055,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.957T>C",
          "hgvs_p": "p.Asp319Asp",
          "transcript": "NM_001353196.2",
          "protein_id": "NP_001340125.1",
          "transcript_support_level": null,
          "aa_start": 319,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 957,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 1143,
          "cdna_end": null,
          "cdna_length": 2967,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.957T>C",
          "hgvs_p": "p.Asp319Asp",
          "transcript": "ENST00000678303.1",
          "protein_id": "ENSP00000503696.1",
          "transcript_support_level": null,
          "aa_start": 319,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 957,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 1113,
          "cdna_end": null,
          "cdna_length": 2573,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.951T>C",
          "hgvs_p": "p.Asp317Asp",
          "transcript": "NM_001353197.2",
          "protein_id": "NP_001340126.2",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 693,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 2082,
          "cdna_start": 1147,
          "cdna_end": null,
          "cdna_length": 2971,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.951T>C",
          "hgvs_p": "p.Asp317Asp",
          "transcript": "NM_001353198.2",
          "protein_id": "NP_001340127.2",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 693,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 2082,
          "cdna_start": 1848,
          "cdna_end": null,
          "cdna_length": 3672,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.885T>C",
          "hgvs_p": "p.Asp295Asp",
          "transcript": "NM_001077366.2",
          "protein_id": "NP_001070834.1",
          "transcript_support_level": null,
          "aa_start": 295,
          "aa_end": null,
          "aa_length": 671,
          "cds_start": 885,
          "cds_end": null,
          "cds_length": 2016,
          "cdna_start": 1081,
          "cdna_end": null,
          "cdna_length": 2905,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.885T>C",
          "hgvs_p": "p.Asp295Asp",
          "transcript": "NM_001353194.2",
          "protein_id": "NP_001340123.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 671,
          "cds_start": 885,
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          "cds_length": 2016,
          "cdna_start": 1321,
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          "cdna_length": 3145,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.885T>C",
          "hgvs_p": "p.Asp295Asp",
          "transcript": "ENST00000341012.13",
          "protein_id": "ENSP00000343034.7",
          "transcript_support_level": 2,
          "aa_start": 295,
          "aa_end": null,
          "aa_length": 671,
          "cds_start": 885,
          "cds_end": null,
          "cds_length": 2016,
          "cdna_start": 1104,
          "cdna_end": null,
          "cdna_length": 2935,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp",
          "transcript": "NM_001374690.1",
          "protein_id": "NP_001361619.1",
          "transcript_support_level": null,
          "aa_start": 349,
          "aa_end": null,
          "aa_length": 652,
          "cds_start": 1047,
          "cds_end": null,
          "cds_length": 1959,
          "cdna_start": 1233,
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          "cdna_length": 2838,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.762T>C",
          "hgvs_p": "p.Asp254Asp",
          "transcript": "NM_001353199.2",
          "protein_id": "NP_001340128.2",
          "transcript_support_level": null,
          "aa_start": 254,
          "aa_end": null,
          "aa_length": 630,
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          "cdna_start": 1040,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.696T>C",
          "hgvs_p": "p.Asp232Asp",
          "transcript": "NM_001136114.2",
          "protein_id": "NP_001129586.1",
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          "cds_start": 696,
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          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "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": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.696T>C",
          "hgvs_p": "p.Asp232Asp",
          "transcript": "NM_001353195.2",
          "protein_id": "NP_001340124.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 608,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1827,
          "cdna_start": 1126,
          "cdna_end": null,
          "cdna_length": 2950,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
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      "computational_score_selected": -0.5899999737739563,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.59,
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      "phylop100way_score": -1.54,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
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      "mitotip_score": null,
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      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
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          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Very_Strong",
            "BP7",
            "BA1"
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          "verdict": "Benign",
          "transcript": "ENST00000402686.8",
          "gene_symbol": "POMT1",
          "hgnc_id": 9202,
          "effects": [
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          "inheritance_mode": "AR",
          "hgvs_c": "c.1047T>C",
          "hgvs_p": "p.Asp349Asp"
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      "clinvar_disease": " type A1, type B1,Autosomal recessive limb-girdle muscular dystrophy type 2K,Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies),Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability),Walker-Warburg congenital muscular dystrophy,not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:7",
      "phenotype_combined": "not specified|Autosomal recessive limb-girdle muscular dystrophy type 2K;Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1;Walker-Warburg congenital muscular dystrophy|Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1|Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1|Autosomal recessive limb-girdle muscular dystrophy type 2K|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}