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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: 11-17393697-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=17393697&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 17393697,
      "ref": "C",
      "alt": "A",
      "effect": "splice_region_variant,synonymous_variant",
      "transcript": "ENST00000389817.8",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4608G>T",
          "hgvs_p": "p.Ala1536Ala",
          "transcript": "NM_000352.6",
          "protein_id": "NP_000343.2",
          "transcript_support_level": null,
          "aa_start": 1536,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4608,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4677,
          "cdna_end": null,
          "cdna_length": 4921,
          "mane_select": "ENST00000389817.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4608G>T",
          "hgvs_p": "p.Ala1536Ala",
          "transcript": "ENST00000389817.8",
          "protein_id": "ENSP00000374467.4",
          "transcript_support_level": 1,
          "aa_start": 1536,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4608,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4677,
          "cdna_end": null,
          "cdna_length": 4921,
          "mane_select": "NM_000352.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4674G>T",
          "hgvs_p": "p.Ala1558Ala",
          "transcript": "NM_001351295.2",
          "protein_id": "NP_001338224.1",
          "transcript_support_level": null,
          "aa_start": 1558,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 4674,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 4743,
          "cdna_end": null,
          "cdna_length": 5374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4674G>T",
          "hgvs_p": "p.Ala1558Ala",
          "transcript": "ENST00000644772.1",
          "protein_id": "ENSP00000494321.1",
          "transcript_support_level": null,
          "aa_start": 1558,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 4674,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 4705,
          "cdna_end": null,
          "cdna_length": 5336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4611G>T",
          "hgvs_p": "p.Ala1537Ala",
          "transcript": "NM_001287174.3",
          "protein_id": "NP_001274103.1",
          "transcript_support_level": null,
          "aa_start": 1537,
          "aa_end": null,
          "aa_length": 1582,
          "cds_start": 4611,
          "cds_end": null,
          "cds_length": 4749,
          "cdna_start": 4680,
          "cdna_end": null,
          "cdna_length": 4924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4611G>T",
          "hgvs_p": "p.Ala1537Ala",
          "transcript": "ENST00000302539.9",
          "protein_id": "ENSP00000303960.4",
          "transcript_support_level": 5,
          "aa_start": 1537,
          "aa_end": null,
          "aa_length": 1582,
          "cds_start": 4611,
          "cds_end": null,
          "cds_length": 4749,
          "cdna_start": 4680,
          "cdna_end": null,
          "cdna_length": 4924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4608G>T",
          "hgvs_p": "p.Ala1536Ala",
          "transcript": "NM_001351296.2",
          "protein_id": "NP_001338225.1",
          "transcript_support_level": null,
          "aa_start": 1536,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4608,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4677,
          "cdna_end": null,
          "cdna_length": 5308,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4608G>T",
          "hgvs_p": "p.Ala1536Ala",
          "transcript": "ENST00000643260.1",
          "protein_id": "ENSP00000494450.1",
          "transcript_support_level": null,
          "aa_start": 1536,
          "aa_end": null,
          "aa_length": 1581,
          "cds_start": 4608,
          "cds_end": null,
          "cds_length": 4746,
          "cdna_start": 4677,
          "cdna_end": null,
          "cdna_length": 4903,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4605G>T",
          "hgvs_p": "p.Ala1535Ala",
          "transcript": "NM_001351297.2",
          "protein_id": "NP_001338226.1",
          "transcript_support_level": null,
          "aa_start": 1535,
          "aa_end": null,
          "aa_length": 1580,
          "cds_start": 4605,
          "cds_end": null,
          "cds_length": 4743,
          "cdna_start": 4674,
          "cdna_end": null,
          "cdna_length": 5305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4605G>T",
          "hgvs_p": "p.Ala1535Ala",
          "transcript": "ENST00000642271.1",
          "protein_id": "ENSP00000493749.1",
          "transcript_support_level": null,
          "aa_start": 1535,
          "aa_end": null,
          "aa_length": 1580,
          "cds_start": 4605,
          "cds_end": null,
          "cds_length": 4743,
          "cdna_start": 4640,
          "cdna_end": null,
          "cdna_length": 4866,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4575G>T",
          "hgvs_p": "p.Ala1525Ala",
          "transcript": "ENST00000646902.1",
          "protein_id": "ENSP00000494101.1",
          "transcript_support_level": null,
          "aa_start": 1525,
          "aa_end": null,
          "aa_length": 1570,
          "cds_start": 4575,
          "cds_end": null,
          "cds_length": 4713,
          "cdna_start": 4643,
          "cdna_end": null,
          "cdna_length": 4874,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4491G>T",
          "hgvs_p": "p.Ala1497Ala",
          "transcript": "ENST00000683136.1",
          "protein_id": "ENSP00000507768.1",
          "transcript_support_level": null,
          "aa_start": 1497,
          "aa_end": null,
          "aa_length": 1542,
          "cds_start": 4491,
          "cds_end": null,
          "cds_length": 4629,
          "cdna_start": 4587,
          "cdna_end": null,
          "cdna_length": 4819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4449G>T",
          "hgvs_p": "p.Ala1483Ala",
          "transcript": "ENST00000684571.1",
          "protein_id": "ENSP00000506935.1",
          "transcript_support_level": null,
          "aa_start": 1483,
          "aa_end": null,
          "aa_length": 1528,
          "cds_start": 4449,
          "cds_end": null,
          "cds_length": 4587,
          "cdna_start": 4490,
          "cdna_end": null,
          "cdna_length": 4722,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.4359G>T",
          "hgvs_p": "p.Ala1453Ala",
          "transcript": "ENST00000647015.1",
          "protein_id": "ENSP00000495389.1",
          "transcript_support_level": null,
          "aa_start": 1453,
          "aa_end": null,
          "aa_length": 1498,
          "cds_start": 4359,
          "cds_end": null,
          "cds_length": 4497,
          "cdna_start": 4427,
          "cdna_end": null,
          "cdna_length": 4642,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.2661G>T",
          "hgvs_p": "p.Ala887Ala",
          "transcript": "ENST00000642579.1",
          "protein_id": "ENSP00000496714.1",
          "transcript_support_level": null,
          "aa_start": 887,
          "aa_end": null,
          "aa_length": 932,
          "cds_start": 2661,
          "cds_end": null,
          "cds_length": 2799,
          "cdna_start": 2662,
          "cdna_end": null,
          "cdna_length": 2893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "c.1197G>T",
          "hgvs_p": "p.Ala399Ala",
          "transcript": "ENST00000528374.2",
          "protein_id": "ENSP00000433638.2",
          "transcript_support_level": 5,
          "aa_start": 399,
          "aa_end": null,
          "aa_length": 444,
          "cds_start": 1197,
          "cds_end": null,
          "cds_length": 1335,
          "cdna_start": 1199,
          "cdna_end": null,
          "cdna_length": 1443,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.4209G>T",
          "hgvs_p": null,
          "transcript": "ENST00000524561.2",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 4441,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.503G>T",
          "hgvs_p": null,
          "transcript": "ENST00000525022.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.543G>T",
          "hgvs_p": null,
          "transcript": "ENST00000526037.6",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 775,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.*295G>T",
          "hgvs_p": null,
          "transcript": "ENST00000526168.5",
          "protein_id": "ENSP00000437233.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
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          "cdna_start": null,
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        },
        {
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          "protein_coding": false,
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            "intron_variant"
          ],
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          "exon_count": 23,
          "intron_rank": 22,
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          "transcript": "ENST00000643925.1",
          "protein_id": "ENSP00000495697.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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        },
        {
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 31,
          "intron_rank": 30,
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          "gene_symbol": "ABCC8",
          "gene_hgnc_id": 59,
          "hgvs_c": "n.*3203-717G>T",
          "hgvs_p": null,
          "transcript": "ENST00000644757.1",
          "protein_id": "ENSP00000495085.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_length": 5025,
          "mane_select": null,
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      ],
      "gene_symbol": "ABCC8",
      "gene_hgnc_id": 59,
      "dbsnp": "rs1439464815",
      "frequency_reference_population": 6.8406376e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84064e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.28999999165534973,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.8740000128746033,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.29,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.299,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.68,
      "spliceai_max_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.999655408763165,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 3,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3",
      "acmg_by_gene": [
        {
          "score": 3,
          "benign_score": 0,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PP3"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000389817.8",
          "gene_symbol": "ABCC8",
          "hgnc_id": 59,
          "effects": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD,Unknown,SD",
          "hgvs_c": "c.4608G>T",
          "hgvs_p": "p.Ala1536Ala"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}