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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: 1-45331137-TGTAGGAAACACAAGGAAGTACAACAAAGACAACAAAG-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=45331137&ref=TGTAGGAAACACAAGGAAGTACAACAAAGACAACAAAG&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 45331137,
      "ref": "TGTAGGAAACACAAGGAAGTACAACAAAGACAACAAAG",
      "alt": "T",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001128425.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1476+8_1476+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "NM_001128425.2",
          "protein_id": "NP_001121897.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 549,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1650,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "ENST00000710952.2",
          "biotype": "protein_coding",
          "feature": "NM_001128425.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1476+8_1476+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000710952.2",
          "protein_id": "ENSP00000518552.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 549,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1650,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "NM_001128425.2",
          "biotype": "protein_coding",
          "feature": "ENST00000710952.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1392+8_1392+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "NM_001048174.2",
          "protein_id": "NP_001041639.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000456914.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001048174.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1392+8_1392+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000456914.7",
          "protein_id": "ENSP00000407590.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 521,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1566,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001048174.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000456914.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1467+8_1467+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000372098.7",
          "protein_id": "ENSP00000361170.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 546,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1641,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372098.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1437+8_1437+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000372110.7",
          "protein_id": "ENSP00000361182.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372110.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1434+8_1434+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000372115.7",
          "protein_id": "ENSP00000361187.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372115.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1425+8_1425+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000448481.5",
          "protein_id": "ENSP00000409718.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 532,
          "cds_start": null,
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          "cds_length": 1599,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000448481.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "MUTYH",
          "gene_hgnc_id": 7527,
          "hgvs_c": "c.1395+8_1395+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000354383.10",
          "protein_id": "ENSP00000346354.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 522,
          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 14,
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          "gene_symbol": "MUTYH",
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          "hgvs_c": "c.1392+8_1392+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000355498.6",
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          "aa_start": null,
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          "aa_length": 521,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
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        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
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          "exon_count": 17,
          "intron_rank": 15,
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          "gene_symbol": "MUTYH",
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          "hgvs_c": "c.1392+8_1392+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
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        {
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          "consequences": [
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          "intron_rank": 14,
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          "gene_symbol": "MUTYH",
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          "hgvs_c": "n.*1205+8_*1205+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null,
          "transcript": "ENST00000475516.5",
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          "biotype": "nonsense_mediated_decay",
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        {
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          "consequences": [
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            "intron_variant"
          ],
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          "gene_symbol": "MUTYH",
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          "hgvs_c": "n.1980+8_1980+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
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        {
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          "gene_symbol": "MUTYH",
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          "gene_symbol": "MUTYH",
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          "transcript": "NM_001407083.1",
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          "biotype": "protein_coding",
          "feature": "NM_001407083.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "intron_rank": 14,
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          "gene_symbol": "MUTYH",
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        {
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          "hgvs_c": "n.*1626_*1662delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
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          "transcript": "ENST00000672593.1",
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000672593.1"
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      ],
      "gene_symbol": "MUTYH",
      "gene_hgnc_id": 7527,
      "dbsnp": "rs765210829",
      "frequency_reference_population": 0.0000018620217,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 3,
      "gnomad_exomes_af": 0.00000137077,
      "gnomad_genomes_af": 0.00000657367,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 3.467,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP6_Moderate",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001128425.2",
          "gene_symbol": "MUTYH",
          "hgnc_id": 7527,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.1476+8_1476+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000671898.1",
          "gene_symbol": "ENSG00000288208",
          "hgnc_id": null,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.1980+8_1980+44delCTTTGTTGTCTTTGTTGTACTTCCTTGTGTTTCCTAC",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Familial adenomatous polyposis 2",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Familial adenomatous polyposis 2",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}