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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: 5-126544987-GC-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=126544987&ref=GC&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 126544987,
      "ref": "GC",
      "alt": "G",
      "effect": "frameshift_variant",
      "transcript": "NM_001182.5",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1597delG",
          "hgvs_p": "p.Ala533fs",
          "transcript": "NM_001182.5",
          "protein_id": "NP_001173.2",
          "transcript_support_level": null,
          "aa_start": 533,
          "aa_end": null,
          "aa_length": 539,
          "cds_start": 1597,
          "cds_end": null,
          "cds_length": 1620,
          "cdna_start": 1618,
          "cdna_end": null,
          "cdna_length": 4765,
          "mane_select": "ENST00000409134.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001182.5"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1597delG",
          "hgvs_p": "p.Ala533fs",
          "transcript": "ENST00000409134.8",
          "protein_id": "ENSP00000387123.3",
          "transcript_support_level": 1,
          "aa_start": 533,
          "aa_end": null,
          "aa_length": 539,
          "cds_start": 1597,
          "cds_end": null,
          "cds_length": 1620,
          "cdna_start": 1618,
          "cdna_end": null,
          "cdna_length": 4765,
          "mane_select": "NM_001182.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409134.8"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1642delG",
          "hgvs_p": "p.Ala548fs",
          "transcript": "ENST00000636879.1",
          "protein_id": "ENSP00000490811.1",
          "transcript_support_level": 5,
          "aa_start": 548,
          "aa_end": null,
          "aa_length": 554,
          "cds_start": 1642,
          "cds_end": null,
          "cds_length": 1665,
          "cdna_start": 1663,
          "cdna_end": null,
          "cdna_length": 2501,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636879.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1639delG",
          "hgvs_p": "p.Ala547fs",
          "transcript": "ENST00000939100.1",
          "protein_id": "ENSP00000609159.1",
          "transcript_support_level": null,
          "aa_start": 547,
          "aa_end": null,
          "aa_length": 553,
          "cds_start": 1639,
          "cds_end": null,
          "cds_length": 1662,
          "cdna_start": 1689,
          "cdna_end": null,
          "cdna_length": 3447,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000939100.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1627delG",
          "hgvs_p": "p.Ala543fs",
          "transcript": "ENST00000865294.1",
          "protein_id": "ENSP00000535353.1",
          "transcript_support_level": null,
          "aa_start": 543,
          "aa_end": null,
          "aa_length": 549,
          "cds_start": 1627,
          "cds_end": null,
          "cds_length": 1650,
          "cdna_start": 1641,
          "cdna_end": null,
          "cdna_length": 1871,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865294.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1618delG",
          "hgvs_p": "p.Ala540fs",
          "transcript": "ENST00000865298.1",
          "protein_id": "ENSP00000535357.1",
          "transcript_support_level": null,
          "aa_start": 540,
          "aa_end": null,
          "aa_length": 546,
          "cds_start": 1618,
          "cds_end": null,
          "cds_length": 1641,
          "cdna_start": 1618,
          "cdna_end": null,
          "cdna_length": 1849,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865298.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1594delG",
          "hgvs_p": "p.Ala532fs",
          "transcript": "ENST00000939101.1",
          "protein_id": "ENSP00000609160.1",
          "transcript_support_level": null,
          "aa_start": 532,
          "aa_end": null,
          "aa_length": 538,
          "cds_start": 1594,
          "cds_end": null,
          "cds_length": 1617,
          "cdna_start": 1643,
          "cdna_end": null,
          "cdna_length": 2506,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000939101.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1588delG",
          "hgvs_p": "p.Ala530fs",
          "transcript": "ENST00000637272.1",
          "protein_id": "ENSP00000489686.1",
          "transcript_support_level": 5,
          "aa_start": 530,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1588,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": 1609,
          "cdna_end": null,
          "cdna_length": 2554,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000637272.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1588delG",
          "hgvs_p": "p.Ala530fs",
          "transcript": "ENST00000865293.1",
          "protein_id": "ENSP00000535352.1",
          "transcript_support_level": null,
          "aa_start": 530,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 1588,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": 1609,
          "cdna_end": null,
          "cdna_length": 1839,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865293.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1558delG",
          "hgvs_p": "p.Ala520fs",
          "transcript": "ENST00000865287.1",
          "protein_id": "ENSP00000535346.1",
          "transcript_support_level": null,
          "aa_start": 520,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1558,
          "cds_end": null,
          "cds_length": 1581,
          "cdna_start": 1640,
          "cdna_end": null,
          "cdna_length": 2663,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865287.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1555delG",
          "hgvs_p": "p.Ala519fs",
          "transcript": "ENST00000865296.1",
          "protein_id": "ENSP00000535355.1",
          "transcript_support_level": null,
          "aa_start": 519,
          "aa_end": null,
          "aa_length": 525,
          "cds_start": 1555,
          "cds_end": null,
          "cds_length": 1578,
          "cdna_start": 1576,
          "cdna_end": null,
          "cdna_length": 1794,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865296.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1519delG",
          "hgvs_p": "p.Ala507fs",
          "transcript": "ENST00000865295.1",
          "protein_id": "ENSP00000535354.1",
          "transcript_support_level": null,
          "aa_start": 507,
          "aa_end": null,
          "aa_length": 513,
          "cds_start": 1519,
          "cds_end": null,
          "cds_length": 1542,
          "cdna_start": 1528,
          "cdna_end": null,
          "cdna_length": 1758,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865295.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1513delG",
          "hgvs_p": "p.Ala505fs",
          "transcript": "NM_001201377.2",
          "protein_id": "NP_001188306.1",
          "transcript_support_level": null,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 511,
          "cds_start": 1513,
          "cds_end": null,
          "cds_length": 1536,
          "cdna_start": 1618,
          "cdna_end": null,
          "cdna_length": 4765,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001201377.2"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1495delG",
          "hgvs_p": "p.Ala499fs",
          "transcript": "ENST00000865291.1",
          "protein_id": "ENSP00000535350.1",
          "transcript_support_level": null,
          "aa_start": 499,
          "aa_end": null,
          "aa_length": 505,
          "cds_start": 1495,
          "cds_end": null,
          "cds_length": 1518,
          "cdna_start": 1516,
          "cdna_end": null,
          "cdna_length": 1748,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865291.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1480delG",
          "hgvs_p": "p.Ala494fs",
          "transcript": "ENST00000865288.1",
          "protein_id": "ENSP00000535347.1",
          "transcript_support_level": null,
          "aa_start": 494,
          "aa_end": null,
          "aa_length": 500,
          "cds_start": 1480,
          "cds_end": null,
          "cds_length": 1503,
          "cdna_start": 1501,
          "cdna_end": null,
          "cdna_length": 2524,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865288.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1477delG",
          "hgvs_p": "p.Ala493fs",
          "transcript": "ENST00000636743.1",
          "protein_id": "ENSP00000489725.1",
          "transcript_support_level": 5,
          "aa_start": 493,
          "aa_end": null,
          "aa_length": 499,
          "cds_start": 1477,
          "cds_end": null,
          "cds_length": 1500,
          "cdna_start": 1498,
          "cdna_end": null,
          "cdna_length": 2332,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636743.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1474delG",
          "hgvs_p": "p.Ala492fs",
          "transcript": "ENST00000865292.1",
          "protein_id": "ENSP00000535351.1",
          "transcript_support_level": null,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": 1474,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": 1495,
          "cdna_end": null,
          "cdna_length": 1726,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865292.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1447delG",
          "hgvs_p": "p.Ala483fs",
          "transcript": "ENST00000960036.1",
          "protein_id": "ENSP00000630095.1",
          "transcript_support_level": null,
          "aa_start": 483,
          "aa_end": null,
          "aa_length": 489,
          "cds_start": 1447,
          "cds_end": null,
          "cds_length": 1470,
          "cdna_start": 1455,
          "cdna_end": null,
          "cdna_length": 1564,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000960036.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1417delG",
          "hgvs_p": "p.Ala473fs",
          "transcript": "ENST00000637206.1",
          "protein_id": "ENSP00000489895.1",
          "transcript_support_level": 5,
          "aa_start": 473,
          "aa_end": null,
          "aa_length": 479,
          "cds_start": 1417,
          "cds_end": null,
          "cds_length": 1440,
          "cdna_start": 1488,
          "cdna_end": null,
          "cdna_length": 2466,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000637206.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH7A1",
          "gene_hgnc_id": 877,
          "hgvs_c": "c.1405delG",
          "hgvs_p": "p.Ala469fs",
          "transcript": "NM_001202404.2",
          "protein_id": "NP_001189333.2",
          "transcript_support_level": null,
          "aa_start": 469,
          "aa_end": null,
          "aa_length": 475,
          "cds_start": 1405,
          "cds_end": null,
          "cds_length": 1428,
          "cdna_start": 1426,
          "cdna_end": null,
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          "cdna_length": 1865,
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000638008.1"
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      ],
      "gene_symbol": "ALDH7A1",
      "gene_hgnc_id": 877,
      "dbsnp": "rs387906574",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": 0.00000205706,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 3,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 6.807,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.03,
      "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": 16,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1_Moderate,PS3,PM2,PP5_Very_Strong",
      "acmg_by_gene": [
        {
          "score": 16,
          "benign_score": 0,
          "pathogenic_score": 16,
          "criteria": [
            "PVS1_Moderate",
            "PS3",
            "PM2",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "NM_001182.5",
          "gene_symbol": "ALDH7A1",
          "hgnc_id": 877,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.1597delG",
          "hgvs_p": "p.Ala533fs"
        }
      ],
      "clinvar_disease": "Abnormality of the nervous system,Pyridoxine-dependent epilepsy,not provided",
      "clinvar_classification": "Pathogenic/Likely pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:2 LP:2",
      "phenotype_combined": "Pyridoxine-dependent epilepsy|not provided|Abnormality of the nervous system",
      "pathogenicity_classification_combined": "Pathogenic/Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.