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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: 4-128871735-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=128871735&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 128871735,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "NM_199320.4",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "NM_199320.4",
          "protein_id": "NP_955352.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000226319.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_199320.4"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000226319.11",
          "protein_id": "ENSP00000226319.6",
          "transcript_support_level": 5,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_199320.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000226319.11"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2101C>G",
          "hgvs_p": "p.Leu701Val",
          "transcript": "ENST00000947587.1",
          "protein_id": "ENSP00000617646.1",
          "transcript_support_level": null,
          "aa_start": 701,
          "aa_end": null,
          "aa_length": 875,
          "cds_start": 2101,
          "cds_end": null,
          "cds_length": 2628,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000947587.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2074C>G",
          "hgvs_p": "p.Leu692Val",
          "transcript": "ENST00000887597.1",
          "protein_id": "ENSP00000557656.1",
          "transcript_support_level": null,
          "aa_start": 692,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": 2074,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000887597.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2074C>G",
          "hgvs_p": "p.Leu692Val",
          "transcript": "ENST00000933993.1",
          "protein_id": "ENSP00000604052.1",
          "transcript_support_level": null,
          "aa_start": 692,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": 2074,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000933993.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2074C>G",
          "hgvs_p": "p.Leu692Val",
          "transcript": "ENST00000933995.1",
          "protein_id": "ENSP00000604054.1",
          "transcript_support_level": null,
          "aa_start": 692,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": 2074,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000933995.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2074C>G",
          "hgvs_p": "p.Leu692Val",
          "transcript": "ENST00000947588.1",
          "protein_id": "ENSP00000617647.1",
          "transcript_support_level": null,
          "aa_start": 692,
          "aa_end": null,
          "aa_length": 866,
          "cds_start": 2074,
          "cds_end": null,
          "cds_length": 2601,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000947588.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "NM_001287439.2",
          "protein_id": "NP_001274368.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001287439.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "NM_001287440.2",
          "protein_id": "NP_001274369.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001287440.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "NM_001287442.1",
          "protein_id": "NP_001274371.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001287442.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "NM_001287443.1",
          "protein_id": "NP_001274372.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001287443.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000512960.5",
          "protein_id": "ENSP00000425730.1",
          "transcript_support_level": 2,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000512960.5"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000610919.4",
          "protein_id": "ENSP00000483219.1",
          "transcript_support_level": 5,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000610919.4"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000611140.4",
          "protein_id": "ENSP00000482212.1",
          "transcript_support_level": 5,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000611140.4"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887598.1",
          "protein_id": "ENSP00000557657.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
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          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000887598.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887600.1",
          "protein_id": "ENSP00000557659.1",
          "transcript_support_level": null,
          "aa_start": 668,
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          "aa_length": 842,
          "cds_start": 2002,
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          "biotype": "protein_coding",
          "feature": "ENST00000887600.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887601.1",
          "protein_id": "ENSP00000557660.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
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          "protein_coding": true,
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          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887603.1",
          "protein_id": "ENSP00000557662.1",
          "transcript_support_level": null,
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          "cds_start": 2002,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "L",
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          "strand": true,
          "consequences": [
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          ],
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887604.1",
          "protein_id": "ENSP00000557663.1",
          "transcript_support_level": null,
          "aa_start": 668,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000887604.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JADE1",
          "gene_hgnc_id": 30027,
          "hgvs_c": "c.2002C>G",
          "hgvs_p": "p.Leu668Val",
          "transcript": "ENST00000887605.1",
          "protein_id": "ENSP00000557664.1",
          "transcript_support_level": null,
          "aa_start": 668,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": 2002,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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      "acmg_classification": "Benign",
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            "BP4_Strong"
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          "verdict": "Likely_benign",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}