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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: 2-219501903-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=219501903&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 219501903,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000313597.10",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_013335.4",
          "protein_id": "NP_037467.2",
          "transcript_support_level": null,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 420,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1263,
          "cdna_start": 363,
          "cdna_end": null,
          "cdna_length": 1522,
          "mane_select": "ENST00000313597.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "ENST00000313597.10",
          "protein_id": "ENSP00000315925.6",
          "transcript_support_level": 1,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 420,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1263,
          "cdna_start": 363,
          "cdna_end": null,
          "cdna_length": 1522,
          "mane_select": "NM_013335.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "ENST00000358215.8",
          "protein_id": "ENSP00000350949.3",
          "transcript_support_level": 1,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 420,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1263,
          "cdna_start": 664,
          "cdna_end": null,
          "cdna_length": 1823,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_001438893.1",
          "protein_id": "NP_001425822.1",
          "transcript_support_level": null,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 363,
          "cdna_end": null,
          "cdna_length": 1681,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_001438894.1",
          "protein_id": "NP_001425823.1",
          "transcript_support_level": null,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 358,
          "cdna_end": null,
          "cdna_length": 1676,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_001438895.1",
          "protein_id": "NP_001425824.1",
          "transcript_support_level": null,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 674,
          "cdna_end": null,
          "cdna_length": 1992,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "ENST00000373917.7",
          "protein_id": "ENSP00000363027.3",
          "transcript_support_level": 5,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 366,
          "cdna_end": null,
          "cdna_length": 1630,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_001374294.1",
          "protein_id": "NP_001361223.1",
          "transcript_support_level": null,
          "aa_start": 99,
          "aa_end": null,
          "aa_length": 420,
          "cds_start": 295,
          "cds_end": null,
          "cds_length": 1263,
          "cdna_start": 358,
          "cdna_end": null,
          "cdna_length": 1517,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_001374295.1",
          "protein_id": "NP_001361224.1",
          "transcript_support_level": null,
          "aa_start": 99,
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          "cdna_start": 679,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_rank": 5,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "GMPPA",
          "gene_hgnc_id": 22923,
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly",
          "transcript": "NM_205847.3",
          "protein_id": "NP_995319.1",
          "transcript_support_level": null,
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          "aa_end": null,
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          "cds_start": 295,
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        {
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        {
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        {
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          "gene_symbol": "GMPPA",
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          "transcript": "ENST00000435316.6",
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        {
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        {
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      "computational_score_selected": 0.9055205583572388,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.05999999865889549,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.872,
      "revel_prediction": "Pathogenic",
      "alphamissense_score": 0.8435,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.48,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 2.52,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.06,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3_Moderate",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PM2",
            "PP3_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000313597.10",
          "gene_symbol": "GMPPA",
          "hgnc_id": 22923,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.295C>G",
          "hgvs_p": "p.Arg99Gly"
        },
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PM2",
            "PP3_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000429882.1",
          "gene_symbol": "ASIC4-AS1",
          "hgnc_id": 40960,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.182+14793G>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
}