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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: 17-82037630-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=82037630&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 82037630,
      "ref": "C",
      "alt": "T",
      "effect": "splice_donor_variant,intron_variant",
      "transcript": "NM_016286.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "NM_016286.4",
          "protein_id": "NP_057370.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 244,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000306869.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_016286.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000306869.7",
          "protein_id": "ENSP00000303356.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 244,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_016286.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000306869.7"
        },
        {
          "aa_ref": "G",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.53G>A",
          "hgvs_p": "p.Gly18Asp",
          "transcript": "ENST00000579155.1",
          "protein_id": "ENSP00000462226.1",
          "transcript_support_level": 5,
          "aa_start": 18,
          "aa_end": null,
          "aa_length": 140,
          "cds_start": 53,
          "cds_end": null,
          "cds_length": 423,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000579155.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859713.1",
          "protein_id": "ENSP00000529772.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 261,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000859713.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859716.1",
          "protein_id": "ENSP00000529775.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 258,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 777,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000859716.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859702.1",
          "protein_id": "ENSP00000529761.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000859702.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859705.1",
          "protein_id": "ENSP00000529764.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 252,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 759,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000859705.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000938655.1",
          "protein_id": "ENSP00000608714.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 251,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 756,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000938655.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859708.1",
          "protein_id": "ENSP00000529767.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 249,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000859708.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859721.1",
          "protein_id": "ENSP00000529780.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 249,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "NM_001195218.1",
          "protein_id": "NP_001182147.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 729,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001195218.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 1,
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          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859704.1",
          "protein_id": "ENSP00000529763.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
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          "exon_count": 8,
          "intron_rank": 1,
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          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859710.1",
          "protein_id": "ENSP00000529769.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859718.1",
          "protein_id": "ENSP00000529777.1",
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        {
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          "intron_rank": 1,
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          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
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          "transcript": "ENST00000859717.1",
          "protein_id": "ENSP00000529776.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000859717.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859720.1",
          "protein_id": "ENSP00000529779.1",
          "transcript_support_level": null,
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          "cds_start": null,
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
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          "transcript": "ENST00000859706.1",
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          ],
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          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.46+1G>A",
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          "protein_id": "ENSP00000464507.1",
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        {
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          "consequences": [
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            "intron_variant"
          ],
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          "intron_rank": 1,
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          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
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          "aa_start": null,
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          "cds_start": null,
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          "cds_length": 671,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000582900.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DCXR",
          "gene_hgnc_id": 18985,
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000859709.1",
          "protein_id": "ENSP00000529768.1",
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          "aa_start": null,
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          "cds_start": null,
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      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": 0.1424,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.24,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 3.491,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.98,
      "spliceai_max_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.999989917668626,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "NM_016286.4",
          "gene_symbol": "DCXR",
          "hgnc_id": 18985,
          "effects": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.52+1G>A",
          "hgvs_p": null
        },
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PP3_Strong"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000582558.3",
          "gene_symbol": "DCXR-DT",
          "hgnc_id": 54083,
          "effects": [
            "upstream_gene_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-212C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Essential pentosuria",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "Essential pentosuria",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}