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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: 1-37997453-CG-TA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=37997453&ref=CG&alt=TA&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PP3"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "FHL3",
          "hgnc_id": 3704,
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "inheritance_mode": "AD",
          "pathogenic_score": 1,
          "score": 1,
          "transcript": "NM_004468.5",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PP3",
      "acmg_score": 1,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "TA",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "1",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": null,
      "computational_score_selected": null,
      "computational_source_selected": null,
      "consequences": [
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1656,
          "cdna_start": 973,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_004468.5",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000373016.4",
          "protein_coding": true,
          "protein_id": "NP_004459.2",
          "strand": false,
          "transcript": "NM_004468.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 1656,
          "cdna_start": 973,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000373016.4",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_004468.5",
          "protein_coding": true,
          "protein_id": "ENSP00000362107.3",
          "strand": false,
          "transcript": "ENST00000373016.4",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1468,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 5,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000485803.5",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "n.784_785delCGinsTA",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000485803.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1662,
          "cdna_start": 973,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000850578.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000520866.1",
          "strand": false,
          "transcript": "ENST00000850578.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1559,
          "cdna_start": 876,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882670.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552729.1",
          "strand": false,
          "transcript": "ENST00000882670.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1592,
          "cdna_start": 904,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882671.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552730.1",
          "strand": false,
          "transcript": "ENST00000882671.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1605,
          "cdna_start": 919,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 7,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882672.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552731.1",
          "strand": false,
          "transcript": "ENST00000882672.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1663,
          "cdna_start": 1537,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882674.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552733.1",
          "strand": false,
          "transcript": "ENST00000882674.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5182,
          "cdna_start": 2123,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 5,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882675.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552734.1",
          "strand": false,
          "transcript": "ENST00000882675.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2699,
          "cdna_start": 2016,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000938707.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000608766.1",
          "strand": false,
          "transcript": "ENST00000938707.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1639,
          "cdna_start": 949,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956053.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626112.1",
          "strand": false,
          "transcript": "ENST00000956053.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1605,
          "cdna_start": 919,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956054.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626113.1",
          "strand": false,
          "transcript": "ENST00000956054.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1650,
          "cdna_start": 970,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 7,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956055.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626114.1",
          "strand": false,
          "transcript": "ENST00000956055.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1537,
          "cdna_start": 851,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956056.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626115.1",
          "strand": false,
          "transcript": "ENST00000956056.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 280,
          "aa_ref": "P",
          "aa_start": 265,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1974,
          "cdna_start": 1288,
          "cds_end": null,
          "cds_length": 843,
          "cds_start": 794,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956059.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.794_795delCGinsTA",
          "hgvs_p": "p.Pro265Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626118.1",
          "strand": false,
          "transcript": "ENST00000956059.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 279,
          "aa_ref": "P",
          "aa_start": 264,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1577,
          "cdna_start": 888,
          "cds_end": null,
          "cds_length": 840,
          "cds_start": 791,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000938708.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.791_792delCGinsTA",
          "hgvs_p": "p.Pro264Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000608767.1",
          "strand": false,
          "transcript": "ENST00000938708.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 279,
          "aa_ref": "P",
          "aa_start": 264,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1625,
          "cdna_start": 945,
          "cds_end": null,
          "cds_length": 840,
          "cds_start": 791,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000956058.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.791_792delCGinsTA",
          "hgvs_p": "p.Pro264Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000626117.1",
          "strand": false,
          "transcript": "ENST00000956058.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 264,
          "aa_ref": "P",
          "aa_start": 249,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1606,
          "cdna_start": 925,
          "cds_end": null,
          "cds_length": 795,
          "cds_start": 746,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000882673.1",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.746_747delCGinsTA",
          "hgvs_p": "p.Pro249Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000552732.1",
          "strand": false,
          "transcript": "ENST00000882673.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 172,
          "aa_ref": "P",
          "aa_start": 157,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1480,
          "cdna_start": 797,
          "cds_end": null,
          "cds_length": 519,
          "cds_start": 470,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 5,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001243878.2",
          "gene_hgnc_id": 3704,
          "gene_symbol": "FHL3",
          "hgvs_c": "c.470_471delCGinsTA",
          "hgvs_p": "p.Pro157Leu",
          "intron_rank": null,
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}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.