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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: 2-178616626-GCG-CAA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=178616626&ref=GCG&alt=CAA&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "missense_variant",
            "splice_region_variant"
          ],
          "gene_symbol": "TTN",
          "hgnc_id": 12403,
          "hgvs_c": "c.48163_48165delCGCinsTTG",
          "hgvs_p": "p.Arg16055Leu",
          "inheritance_mode": "AD,AR",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "NM_001267550.2",
          "verdict": "Uncertain_significance"
        },
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "gene_symbol": "ENSG00000271141",
          "hgnc_id": null,
          "hgvs_c": "n.46_48delGCGinsCAA",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "ENST00000605334.1",
          "verdict": "Uncertain_significance"
        },
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "TTN-AS1",
          "hgnc_id": 44124,
          "hgvs_c": "n.1571+1252_1571+1254delGCGinsCAA",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "ENST00000456053.5",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_score": 0,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "CAA",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "2",
      "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": 35991,
          "aa_ref": "R",
          "aa_start": 16055,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 109224,
          "cdna_start": 48390,
          "cds_end": null,
          "cds_length": 107976,
          "cds_start": 48163,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 363,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001267550.2",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.48163_48165delCGCinsTTG",
          "hgvs_p": "p.Arg16055Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000589042.5",
          "protein_coding": true,
          "protein_id": "NP_001254479.2",
          "strand": false,
          "transcript": "NM_001267550.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35991,
          "aa_ref": "R",
          "aa_start": 16055,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 109224,
          "cdna_start": 48390,
          "cds_end": null,
          "cds_length": 107976,
          "cds_start": 48163,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 363,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000589042.5",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.48163_48165delCGCinsTTG",
          "hgvs_p": "p.Arg16055Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001267550.2",
          "protein_coding": true,
          "protein_id": "ENSP00000467141.1",
          "strand": false,
          "transcript": "ENST00000589042.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35939,
          "aa_ref": "R",
          "aa_start": 16003,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 109068,
          "cdna_start": 48234,
          "cds_end": null,
          "cds_length": 107820,
          "cds_start": 48007,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 361,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000446966.2",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.48007_48009delCGCinsTTG",
          "hgvs_p": "p.Arg16003Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000408004.2",
          "strand": false,
          "transcript": "ENST00000446966.2",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35899,
          "aa_ref": "R",
          "aa_start": 15963,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 108948,
          "cdna_start": 48114,
          "cds_end": null,
          "cds_length": 107700,
          "cds_start": 47887,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 361,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000436599.2",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.47887_47889delCGCinsTTG",
          "hgvs_p": "p.Arg15963Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000405517.2",
          "strand": false,
          "transcript": "ENST00000436599.2",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35805,
          "aa_ref": "R",
          "aa_start": 15869,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 108666,
          "cdna_start": 47832,
          "cds_end": null,
          "cds_length": 107418,
          "cds_start": 47605,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 356,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000426232.6",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.47605_47607delCGCinsTTG",
          "hgvs_p": "p.Arg15869Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000392336.2",
          "strand": false,
          "transcript": "ENST00000426232.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35991,
          "aa_ref": "R",
          "aa_start": 16055,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 109488,
          "cdna_start": 48654,
          "cds_end": null,
          "cds_length": 107976,
          "cds_start": 48163,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 365,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000412264.2",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.48163_48165delCGCinsTTG",
          "hgvs_p": "p.Arg16055Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000394672.2",
          "strand": false,
          "transcript": "ENST00000412264.2",
          "transcript_support_level": 3
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35963,
          "aa_ref": "R",
          "aa_start": 16027,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 109140,
          "cdna_start": 48306,
          "cds_end": null,
          "cds_length": 107892,
          "cds_start": 48079,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 362,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000425332.3",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.48079_48081delCGCinsTTG",
          "hgvs_p": "p.Arg16027Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000396805.3",
          "strand": false,
          "transcript": "ENST00000425332.3",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 35853,
          "aa_ref": "R",
          "aa_start": 15917,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 108810,
          "cdna_start": 47976,
          "cds_end": null,
          "cds_length": 107562,
          "cds_start": 47749,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 360,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000715174.1",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.47749_47751delCGCinsTTG",
          "hgvs_p": "p.Arg15917Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000520370.1",
          "strand": false,
          "transcript": "ENST00000715174.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 34350,
          "aa_ref": "R",
          "aa_start": 14414,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 104301,
          "cdna_start": 43467,
          "cds_end": null,
          "cds_length": 103053,
          "cds_start": 43240,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 313,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001256850.1",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.43240_43242delCGCinsTTG",
          "hgvs_p": "p.Arg14414Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001243779.1",
          "strand": false,
          "transcript": "NM_001256850.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 34350,
          "aa_ref": "R",
          "aa_start": 14414,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 104301,
          "cdna_start": 43467,
          "cds_end": null,
          "cds_length": 103053,
          "cds_start": 43240,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 313,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000591111.5",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.43240_43242delCGCinsTTG",
          "hgvs_p": "p.Arg14414Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000465570.1",
          "strand": false,
          "transcript": "ENST00000591111.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 33423,
          "aa_ref": "R",
          "aa_start": 13487,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 101520,
          "cdna_start": 40686,
          "cds_end": null,
          "cds_length": 100272,
          "cds_start": 40459,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 312,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_133378.4",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.40459_40461delCGCinsTTG",
          "hgvs_p": "p.Arg13487Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_596869.4",
          "strand": false,
          "transcript": "NM_133378.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 33423,
          "aa_ref": "R",
          "aa_start": 13487,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 101520,
          "cdna_start": 40686,
          "cds_end": null,
          "cds_length": 100272,
          "cds_start": 40459,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 312,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000342992.11",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.40459_40461delCGCinsTTG",
          "hgvs_p": "p.Arg13487Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000343764.6",
          "strand": false,
          "transcript": "ENST00000342992.11",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 27118,
          "aa_ref": "R",
          "aa_start": 7182,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 82605,
          "cdna_start": 21771,
          "cds_end": null,
          "cds_length": 81357,
          "cds_start": 21544,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 192,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_133437.4",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.21544_21546delCGCinsTTG",
          "hgvs_p": "p.Arg7182Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_597681.4",
          "strand": false,
          "transcript": "NM_133437.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 27118,
          "aa_ref": "R",
          "aa_start": 7182,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 82380,
          "cdna_start": 21546,
          "cds_end": null,
          "cds_length": 81357,
          "cds_start": 21544,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 191,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000342175.12",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.21544_21546delCGCinsTTG",
          "hgvs_p": "p.Arg7182Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000340554.6",
          "strand": false,
          "transcript": "ENST00000342175.12",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 27051,
          "aa_ref": "R",
          "aa_start": 7115,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 82404,
          "cdna_start": 21570,
          "cds_end": null,
          "cds_length": 81156,
          "cds_start": 21343,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 192,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_133432.3",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.21343_21345delCGCinsTTG",
          "hgvs_p": "p.Arg7115Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_597676.3",
          "strand": false,
          "transcript": "NM_133432.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 27051,
          "aa_ref": "R",
          "aa_start": 7115,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 82179,
          "cdna_start": 21345,
          "cds_end": null,
          "cds_length": 81156,
          "cds_start": 21343,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 191,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000359218.11",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.21343_21345delCGCinsTTG",
          "hgvs_p": "p.Arg7115Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000352154.5",
          "strand": false,
          "transcript": "ENST00000359218.11",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 26926,
          "aa_ref": "R",
          "aa_start": 6990,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 82029,
          "cdna_start": 21195,
          "cds_end": null,
          "cds_length": 80781,
          "cds_start": 20968,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_count": 191,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_003319.4",
          "gene_hgnc_id": 12403,
          "gene_symbol": "TTN",
          "hgvs_c": "c.20968_20970delCGCinsTTG",
          "hgvs_p": "p.Arg6990Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_003310.4",
          "strand": false,
          "transcript": "NM_003319.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": 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.