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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: 2-37646324-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=37646324&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 37646324,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000295324.4",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_006449.5",
          "protein_id": "NP_006440.2",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 716,
          "cdna_end": null,
          "cdna_length": 5096,
          "mane_select": "ENST00000295324.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "ENST00000295324.4",
          "protein_id": "ENSP00000295324.3",
          "transcript_support_level": 1,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 716,
          "cdna_end": null,
          "cdna_length": 5096,
          "mane_select": "NM_006449.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_001270436.2",
          "protein_id": "NP_001257365.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 602,
          "cdna_end": null,
          "cdna_length": 4982,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_001270437.2",
          "protein_id": "NP_001257366.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 658,
          "cdna_end": null,
          "cdna_length": 5038,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_001270438.2",
          "protein_id": "NP_001257367.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 634,
          "cdna_end": null,
          "cdna_length": 5014,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_001371569.1",
          "protein_id": "NP_001358498.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 620,
          "cdna_end": null,
          "cdna_length": 5000,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "NM_001371570.1",
          "protein_id": "NP_001358499.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 607,
          "cdna_end": null,
          "cdna_length": 4987,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "ENST00000611976.1",
          "protein_id": "ENSP00000480549.1",
          "transcript_support_level": 3,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 765,
          "cdna_start": 682,
          "cdna_end": null,
          "cdna_length": 5124,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "ENST00000457889.1",
          "protein_id": "ENSP00000403298.1",
          "transcript_support_level": 2,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 214,
          "cds_start": 264,
          "cds_end": null,
          "cds_length": 647,
          "cdna_start": 614,
          "cdna_end": null,
          "cdna_length": 997,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3",
          "gene_hgnc_id": 16943,
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys",
          "transcript": "XM_011532482.4",
          "protein_id": "XP_011530784.1",
          "transcript_support_level": null,
          "aa_start": 88,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 264,
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          "cds_length": 765,
          "cdna_start": 2550,
          "cdna_end": null,
          "cdna_length": 6930,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
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          "gene_symbol": "CDC42EP3-AS1",
          "gene_hgnc_id": 56370,
          "hgvs_c": "n.526-352G>C",
          "hgvs_p": null,
          "transcript": "ENST00000419425.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 548,
          "mane_select": null,
          "mane_plus": null,
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        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
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          "gene_symbol": "CDC42EP3-AS1",
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          "hgvs_c": "n.105-15291G>C",
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          "transcript": "ENST00000702971.2",
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        {
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          "strand": true,
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          ],
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          "gene_symbol": "CDC42EP3-AS1",
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          "hgvs_c": "n.659-15291G>C",
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        {
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          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3-AS1",
          "gene_hgnc_id": 56370,
          "hgvs_c": "n.469+75132G>C",
          "hgvs_p": null,
          "transcript": "ENST00000751609.1",
          "protein_id": null,
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        },
        {
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        {
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          "gene_symbol": "CDC42EP3-AS1",
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          "hgvs_c": "n.282-42734G>C",
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          "transcript": "ENST00000751611.1",
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        {
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          "exon_count": 4,
          "intron_rank": 3,
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          "gene_symbol": "CDC42EP3-AS1",
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        {
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          "gene_hgnc_id": 56370,
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        {
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          "feature": null
        },
        {
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CDC42EP3-AS1",
          "gene_hgnc_id": 56370,
          "hgvs_c": "n.287-15291G>C",
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          "transcript": "ENST00000751616.1",
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          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000295324.4",
          "gene_symbol": "CDC42EP3",
          "hgnc_id": 16943,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.264C>G",
          "hgvs_p": "p.Asn88Lys"
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000419425.1",
          "gene_symbol": "CDC42EP3-AS1",
          "hgnc_id": 56370,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.526-352G>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}