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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: 8-143816646-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143816646&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 143816646,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_078480.3",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1554G>A",
          "hgvs_p": "p.Glu518Glu",
          "transcript": "NM_078480.3",
          "protein_id": "NP_510965.1",
          "transcript_support_level": null,
          "aa_start": 518,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1554,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": 1566,
          "cdna_end": null,
          "cdna_length": 1868,
          "mane_select": "ENST00000526683.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1554G>A",
          "hgvs_p": "p.Glu518Glu",
          "transcript": "ENST00000526683.6",
          "protein_id": "ENSP00000434359.1",
          "transcript_support_level": 1,
          "aa_start": 518,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1554,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": 1566,
          "cdna_end": null,
          "cdna_length": 1868,
          "mane_select": "NM_078480.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1503G>A",
          "hgvs_p": "p.Glu501Glu",
          "transcript": "ENST00000349157.10",
          "protein_id": "ENSP00000322036.7",
          "transcript_support_level": 1,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1503,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": 1552,
          "cdna_end": null,
          "cdna_length": 1821,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1425G>A",
          "hgvs_p": "p.Glu475Glu",
          "transcript": "ENST00000453551.6",
          "protein_id": "ENSP00000402953.2",
          "transcript_support_level": 1,
          "aa_start": 475,
          "aa_end": null,
          "aa_length": 516,
          "cds_start": 1425,
          "cds_end": null,
          "cds_length": 1551,
          "cdna_start": 1573,
          "cdna_end": null,
          "cdna_length": 1842,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1374G>A",
          "hgvs_p": "p.Glu458Glu",
          "transcript": "ENST00000313352.11",
          "protein_id": "ENSP00000322016.7",
          "transcript_support_level": 1,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 499,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 1500,
          "cdna_start": 1535,
          "cdna_end": null,
          "cdna_length": 1804,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1665G>A",
          "hgvs_p": "p.Glu555Glu",
          "transcript": "NM_001362895.2",
          "protein_id": "NP_001349824.1",
          "transcript_support_level": null,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": 1740,
          "cdna_end": null,
          "cdna_length": 2042,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1665G>A",
          "hgvs_p": "p.Glu555Glu",
          "transcript": "NM_001362896.2",
          "protein_id": "NP_001349825.1",
          "transcript_support_level": null,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": 1903,
          "cdna_end": null,
          "cdna_length": 2205,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1665G>A",
          "hgvs_p": "p.Glu555Glu",
          "transcript": "ENST00000533162.2",
          "protein_id": "ENSP00000433403.2",
          "transcript_support_level": 3,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": 1741,
          "cdna_end": null,
          "cdna_length": 1936,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1665G>A",
          "hgvs_p": "p.Glu555Glu",
          "transcript": "ENST00000703847.1",
          "protein_id": "ENSP00000515499.1",
          "transcript_support_level": null,
          "aa_start": 555,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1665,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": 1903,
          "cdna_end": null,
          "cdna_length": 2140,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1629G>A",
          "hgvs_p": "p.Glu543Glu",
          "transcript": "ENST00000533362.2",
          "protein_id": "ENSP00000515502.1",
          "transcript_support_level": 5,
          "aa_start": 543,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1629,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": 1873,
          "cdna_end": null,
          "cdna_length": 2053,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1629G>A",
          "hgvs_p": "p.Glu543Glu",
          "transcript": "ENST00000703850.1",
          "protein_id": "ENSP00000515503.1",
          "transcript_support_level": null,
          "aa_start": 543,
          "aa_end": null,
          "aa_length": 584,
          "cds_start": 1629,
          "cds_end": null,
          "cds_length": 1755,
          "cdna_start": 1780,
          "cdna_end": null,
          "cdna_length": 1952,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1614G>A",
          "hgvs_p": "p.Glu538Glu",
          "transcript": "NM_001362897.2",
          "protein_id": "NP_001349826.1",
          "transcript_support_level": null,
          "aa_start": 538,
          "aa_end": null,
          "aa_length": 579,
          "cds_start": 1614,
          "cds_end": null,
          "cds_length": 1740,
          "cdna_start": 1689,
          "cdna_end": null,
          "cdna_length": 1991,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1554G>A",
          "hgvs_p": "p.Glu518Glu",
          "transcript": "ENST00000703866.1",
          "protein_id": "ENSP00000515511.1",
          "transcript_support_level": null,
          "aa_start": 518,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1554,
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          "cds_length": 1680,
          "cdna_start": 2401,
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          "cdna_length": 2527,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1551G>A",
          "hgvs_p": "p.Glu517Glu",
          "transcript": "NM_001271098.2",
          "protein_id": "NP_001258027.1",
          "transcript_support_level": null,
          "aa_start": 517,
          "aa_end": null,
          "aa_length": 558,
          "cds_start": 1551,
          "cds_end": null,
          "cds_length": 1677,
          "cdna_start": 1563,
          "cdna_end": null,
          "cdna_length": 1865,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1551G>A",
          "hgvs_p": "p.Glu517Glu",
          "transcript": "ENST00000527744.6",
          "protein_id": "ENSP00000436131.2",
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          "cds_start": 1551,
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          "biotype": null,
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        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1503G>A",
          "hgvs_p": "p.Glu501Glu",
          "transcript": "NM_014281.5",
          "protein_id": "NP_055096.2",
          "transcript_support_level": null,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1503,
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          "cdna_start": 1515,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1500G>A",
          "hgvs_p": "p.Glu500Glu",
          "transcript": "NM_001271096.2",
          "protein_id": "NP_001258025.1",
          "transcript_support_level": null,
          "aa_start": 500,
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          "aa_length": 541,
          "cds_start": 1500,
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          "cds_length": 1626,
          "cdna_start": 1512,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 11,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1500G>A",
          "hgvs_p": "p.Glu500Glu",
          "transcript": "ENST00000526459.6",
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        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
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          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1467G>A",
          "hgvs_p": "p.Glu489Glu",
          "transcript": "NM_001271099.2",
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          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "PUF60",
          "gene_hgnc_id": 17042,
          "hgvs_c": "c.1467G>A",
          "hgvs_p": "p.Glu489Glu",
          "transcript": "ENST00000456095.6",
          "protein_id": "ENSP00000395417.2",
          "transcript_support_level": 5,
          "aa_start": 489,
          "aa_end": null,
          "aa_length": 530,
          "cds_start": 1467,
          "cds_end": null,
          "cds_length": 1593,
          "cdna_start": 1467,
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          "cdna_length": 1736,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PUF60",
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      "gene_symbol": "PUF60",
      "gene_hgnc_id": 17042,
      "dbsnp": "rs762422632",
      "frequency_reference_population": 0.000008055731,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 13,
      "gnomad_exomes_af": 0.00000752618,
      "gnomad_genomes_af": 0.0000131411,
      "gnomad_exomes_ac": 11,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.5099999904632568,
      "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": -0.51,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.369,
      "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": -10,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -10,
          "benign_score": 10,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_078480.3",
          "gene_symbol": "PUF60",
          "hgnc_id": 17042,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1554G>A",
          "hgvs_p": "p.Glu518Glu"
        }
      ],
      "clinvar_disease": "PUF60-related disorder",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "PUF60-related disorder",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}