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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: 17-43057069-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=43057069&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 43057069,
      "ref": "C",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000357654.9",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5260G>T",
          "hgvs_p": "p.Glu1754*",
          "transcript": "NM_007294.4",
          "protein_id": "NP_009225.1",
          "transcript_support_level": null,
          "aa_start": 1754,
          "aa_end": null,
          "aa_length": 1863,
          "cds_start": 5260,
          "cds_end": null,
          "cds_length": 5592,
          "cdna_start": 5373,
          "cdna_end": null,
          "cdna_length": 7088,
          "mane_select": "ENST00000357654.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5260G>T",
          "hgvs_p": "p.Glu1754*",
          "transcript": "ENST00000357654.9",
          "protein_id": "ENSP00000350283.3",
          "transcript_support_level": 1,
          "aa_start": 1754,
          "aa_end": null,
          "aa_length": 1863,
          "cds_start": 5260,
          "cds_end": null,
          "cds_length": 5592,
          "cdna_start": 5373,
          "cdna_end": null,
          "cdna_length": 7088,
          "mane_select": "NM_007294.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5323G>T",
          "hgvs_p": "p.Glu1775*",
          "transcript": "ENST00000471181.7",
          "protein_id": "ENSP00000418960.2",
          "transcript_support_level": 1,
          "aa_start": 1775,
          "aa_end": null,
          "aa_length": 1884,
          "cds_start": 5323,
          "cds_end": null,
          "cds_length": 5655,
          "cdna_start": 5555,
          "cdna_end": null,
          "cdna_length": 7270,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5260G>T",
          "hgvs_p": "p.Glu1754*",
          "transcript": "ENST00000470026.6",
          "protein_id": "ENSP00000419274.2",
          "transcript_support_level": 1,
          "aa_start": 1754,
          "aa_end": null,
          "aa_length": 1863,
          "cds_start": 5260,
          "cds_end": null,
          "cds_length": 5592,
          "cdna_start": 5441,
          "cdna_end": null,
          "cdna_length": 7147,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5260G>T",
          "hgvs_p": "p.Glu1754*",
          "transcript": "ENST00000494123.6",
          "protein_id": "ENSP00000419103.2",
          "transcript_support_level": 1,
          "aa_start": 1754,
          "aa_end": null,
          "aa_length": 1863,
          "cds_start": 5260,
          "cds_end": null,
          "cds_length": 5592,
          "cdna_start": 5453,
          "cdna_end": null,
          "cdna_length": 7168,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5260G>T",
          "hgvs_p": "p.Glu1754*",
          "transcript": "ENST00000618469.2",
          "protein_id": "ENSP00000478114.2",
          "transcript_support_level": 1,
          "aa_start": 1754,
          "aa_end": null,
          "aa_length": 1863,
          "cds_start": 5260,
          "cds_end": null,
          "cds_length": 5592,
          "cdna_start": 5907,
          "cdna_end": null,
          "cdna_length": 7613,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5182G>T",
          "hgvs_p": "p.Glu1728*",
          "transcript": "ENST00000477152.6",
          "protein_id": "ENSP00000419988.2",
          "transcript_support_level": 1,
          "aa_start": 1728,
          "aa_end": null,
          "aa_length": 1837,
          "cds_start": 5182,
          "cds_end": null,
          "cds_length": 5514,
          "cdna_start": 5295,
          "cdna_end": null,
          "cdna_length": 7010,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.4372G>T",
          "hgvs_p": "p.Glu1458*",
          "transcript": "ENST00000497488.2",
          "protein_id": "ENSP00000418986.2",
          "transcript_support_level": 1,
          "aa_start": 1458,
          "aa_end": null,
          "aa_length": 1567,
          "cds_start": 4372,
          "cds_end": null,
          "cds_length": 4704,
          "cdna_start": 4620,
          "cdna_end": null,
          "cdna_length": 6335,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.1948G>T",
          "hgvs_p": "p.Glu650*",
          "transcript": "ENST00000478531.6",
          "protein_id": "ENSP00000420412.2",
          "transcript_support_level": 1,
          "aa_start": 650,
          "aa_end": null,
          "aa_length": 759,
          "cds_start": 1948,
          "cds_end": null,
          "cds_length": 2280,
          "cdna_start": 2050,
          "cdna_end": null,
          "cdna_length": 3765,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.1948G>T",
          "hgvs_p": "p.Glu650*",
          "transcript": "ENST00000468300.5",
          "protein_id": "ENSP00000417148.1",
          "transcript_support_level": 1,
          "aa_start": 650,
          "aa_end": null,
          "aa_length": 699,
          "cds_start": 1948,
          "cds_end": null,
          "cds_length": 2100,
          "cdna_start": 2142,
          "cdna_end": null,
          "cdna_length": 3273,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.733G>T",
          "hgvs_p": "p.Glu245*",
          "transcript": "ENST00000591534.5",
          "protein_id": "ENSP00000467329.1",
          "transcript_support_level": 1,
          "aa_start": 245,
          "aa_end": null,
          "aa_length": 354,
          "cds_start": 733,
          "cds_end": null,
          "cds_length": 1065,
          "cdna_start": 835,
          "cdna_end": null,
          "cdna_length": 1282,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.190G>T",
          "hgvs_p": "p.Glu64*",
          "transcript": "ENST00000586385.5",
          "protein_id": "ENSP00000465818.1",
          "transcript_support_level": 1,
          "aa_start": 64,
          "aa_end": null,
          "aa_length": 173,
          "cds_start": 190,
          "cds_end": null,
          "cds_length": 522,
          "cdna_start": 334,
          "cdna_end": null,
          "cdna_length": 781,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "n.*5043G>T",
          "hgvs_p": null,
          "transcript": "ENST00000461221.5",
          "protein_id": "ENSP00000418548.1",
          "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": 5693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "n.*5043G>T",
          "hgvs_p": null,
          "transcript": "ENST00000461221.5",
          "protein_id": "ENSP00000418548.1",
          "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": 5693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.-98-6879G>T",
          "hgvs_p": null,
          "transcript": "ENST00000591849.5",
          "protein_id": "ENSP00000465347.1",
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": 96,
          "cds_start": -4,
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          "cds_length": 291,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 563,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5326G>T",
          "hgvs_p": "p.Glu1776*",
          "transcript": "NM_001407581.1",
          "protein_id": "NP_001394510.1",
          "transcript_support_level": null,
          "aa_start": 1776,
          "aa_end": null,
          "aa_length": 1885,
          "cds_start": 5326,
          "cds_end": null,
          "cds_length": 5658,
          "cdna_start": 5439,
          "cdna_end": null,
          "cdna_length": 7154,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5326G>T",
          "hgvs_p": "p.Glu1776*",
          "transcript": "NM_001407582.1",
          "protein_id": "NP_001394511.1",
          "transcript_support_level": null,
          "aa_start": 1776,
          "aa_end": null,
          "aa_length": 1885,
          "cds_start": 5326,
          "cds_end": null,
          "cds_length": 5658,
          "cdna_start": 5528,
          "cdna_end": null,
          "cdna_length": 7243,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5326G>T",
          "hgvs_p": "p.Glu1776*",
          "transcript": "ENST00000644379.2",
          "protein_id": "ENSP00000496570.2",
          "transcript_support_level": null,
          "aa_start": 1776,
          "aa_end": null,
          "aa_length": 1885,
          "cds_start": 5326,
          "cds_end": null,
          "cds_length": 5658,
          "cdna_start": 5439,
          "cdna_end": null,
          "cdna_length": 6363,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5323G>T",
          "hgvs_p": "p.Glu1775*",
          "transcript": "NM_001407583.1",
          "protein_id": "NP_001394512.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 1884,
          "cds_start": 5323,
          "cds_end": null,
          "cds_length": 5655,
          "cdna_start": 5970,
          "cdna_end": null,
          "cdna_length": 7685,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5323G>T",
          "hgvs_p": "p.Glu1775*",
          "transcript": "NM_001407585.1",
          "protein_id": "NP_001394514.1",
          "transcript_support_level": null,
          "aa_start": 1775,
          "aa_end": null,
          "aa_length": 1884,
          "cds_start": 5323,
          "cds_end": null,
          "cds_length": 5655,
          "cdna_start": 5423,
          "cdna_end": null,
          "cdna_length": 7138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "BRCA1",
          "gene_hgnc_id": 1100,
          "hgvs_c": "c.5323G>T",
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      "acmg_classification": "Pathogenic",
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      "clinvar_disease": " 1, familial, susceptibility to,Breast-ovarian cancer,Hereditary breast ovarian cancer syndrome,Hereditary cancer-predisposing syndrome,not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "reviewed by expert panel",
      "clinvar_submissions_summary": "P:6",
      "phenotype_combined": "Hereditary breast ovarian cancer syndrome|Breast-ovarian cancer, familial, susceptibility to, 1|not provided|Hereditary cancer-predisposing syndrome",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
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  "message": null
}