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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: 17-19657830-C-CA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=19657830&ref=C&alt=CA&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 19657830,
      "ref": "C",
      "alt": "CA",
      "effect": "frameshift_variant",
      "transcript": "ENST00000176643.11",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_000382.3",
          "protein_id": "NP_000373.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 991,
          "cdna_end": null,
          "cdna_length": 3703,
          "mane_select": "ENST00000176643.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000176643.11",
          "protein_id": "ENSP00000176643.6",
          "transcript_support_level": 1,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 991,
          "cdna_end": null,
          "cdna_length": 3703,
          "mane_select": "NM_000382.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000339618.8",
          "protein_id": "ENSP00000345774.4",
          "transcript_support_level": 1,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 991,
          "cdna_end": null,
          "cdna_length": 3828,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "n.519dupA",
          "hgvs_p": null,
          "transcript": "ENST00000476965.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": 1383,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000671878.1",
          "protein_id": "ENSP00000500516.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": 961,
          "cdna_end": null,
          "cdna_length": 2060,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000672465.1",
          "protein_id": "ENSP00000500517.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": 899,
          "cdna_end": null,
          "cdna_length": 2058,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001031806.2",
          "protein_id": "NP_001026976.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 991,
          "cdna_end": null,
          "cdna_length": 3828,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001369136.1",
          "protein_id": "NP_001356065.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 900,
          "cdna_end": null,
          "cdna_length": 3737,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001369137.2",
          "protein_id": "NP_001356066.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 508,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1527,
          "cdna_start": 937,
          "cdna_end": null,
          "cdna_length": 3774,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001369138.2",
          "protein_id": "NP_001356067.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 937,
          "cdna_end": null,
          "cdna_length": 3649,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001369139.1",
          "protein_id": "NP_001356068.1",
          "transcript_support_level": null,
          "aa_start": 257,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 770,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 900,
          "cdna_end": null,
          "cdna_length": 3612,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000579855.5",
          "protein_id": "ENSP00000463637.1",
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          "cds_start": 770,
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          "cdna_start": 869,
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          "feature": null
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 6,
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          "intron_rank": null,
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          "gene_symbol": "ALDH3A2",
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          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000581518.6",
          "protein_id": "ENSP00000461916.2",
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          "cds_start": 770,
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          "cdna_start": 937,
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        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000672357.1",
          "protein_id": "ENSP00000500092.1",
          "transcript_support_level": null,
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          "aa_length": 485,
          "cds_start": 770,
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          "cdna_start": 928,
          "cdna_end": null,
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          "mane_select": null,
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
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          "strand": true,
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          ],
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          "gene_symbol": "ALDH3A2",
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          "hgvs_c": "c.622dupA",
          "hgvs_p": "p.Ile208fs",
          "transcript": "ENST00000672709.1",
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          "cds_start": 623,
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        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "NM_001369146.2",
          "protein_id": "NP_001356075.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 424,
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          "cdna_start": 937,
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          "mane_select": null,
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        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 6,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000673136.1",
          "protein_id": "ENSP00000500380.1",
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          "cdna_start": 920,
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 5,
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          "intron_rank": null,
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          "gene_symbol": "ALDH3A2",
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          "hgvs_c": "c.769dupA",
          "hgvs_p": "p.Ile257fs",
          "transcript": "ENST00000631291.2",
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.658dupA",
          "hgvs_p": "p.Ile220fs",
          "transcript": "ENST00000672567.1",
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 7,
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          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
          "gene_hgnc_id": 403,
          "hgvs_c": "c.190dupA",
          "hgvs_p": "p.Ile64fs",
          "transcript": "NM_001369148.2",
          "protein_id": "NP_001356077.1",
          "transcript_support_level": null,
          "aa_start": 64,
          "aa_end": null,
          "aa_length": 292,
          "cds_start": 191,
          "cds_end": null,
          "cds_length": 879,
          "cdna_start": 1046,
          "cdna_end": null,
          "cdna_length": 3758,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "N?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ALDH3A2",
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      "allele_count_reference_population": 1,
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      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": null,
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      "phylop100way_score": 0.723,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
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      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5",
      "acmg_by_gene": [
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          "verdict": "Pathogenic",
          "transcript": "ENST00000176643.11",
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      "clinvar_disease": "Sjögren-Larsson syndrome",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Sjögren-Larsson syndrome",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}