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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: 21-34834561-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=34834561&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "21",
      "pos": 34834561,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_001754.5",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
          "hgvs_p": "p.Ser218Arg",
          "transcript": "NM_001754.5",
          "protein_id": "NP_001745.2",
          "transcript_support_level": null,
          "aa_start": 218,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": 654,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": 848,
          "cdna_end": null,
          "cdna_length": 5971,
          "mane_select": "ENST00000675419.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
          "hgvs_p": "p.Ser218Arg",
          "transcript": "ENST00000675419.1",
          "protein_id": "ENSP00000501943.1",
          "transcript_support_level": null,
          "aa_start": 218,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": 654,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": 848,
          "cdna_end": null,
          "cdna_length": 5971,
          "mane_select": "NM_001754.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
          "hgvs_p": "p.Ser218Arg",
          "transcript": "ENST00000300305.7",
          "protein_id": "ENSP00000300305.3",
          "transcript_support_level": 1,
          "aa_start": 218,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": 654,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": 1099,
          "cdna_end": null,
          "cdna_length": 6222,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.573C>G",
          "hgvs_p": "p.Ser191Arg",
          "transcript": "ENST00000344691.8",
          "protein_id": "ENSP00000340690.4",
          "transcript_support_level": 1,
          "aa_start": 191,
          "aa_end": null,
          "aa_length": 453,
          "cds_start": 573,
          "cds_end": null,
          "cds_length": 1362,
          "cdna_start": 2151,
          "cdna_end": null,
          "cdna_length": 7274,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.573C>G",
          "hgvs_p": "p.Ser191Arg",
          "transcript": "ENST00000358356.9",
          "protein_id": "ENSP00000351123.5",
          "transcript_support_level": 1,
          "aa_start": 191,
          "aa_end": null,
          "aa_length": 250,
          "cds_start": 573,
          "cds_end": null,
          "cds_length": 753,
          "cdna_start": 2151,
          "cdna_end": null,
          "cdna_length": 2720,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "n.190C>G",
          "hgvs_p": null,
          "transcript": "ENST00000469087.1",
          "protein_id": null,
          "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": 1790,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "n.*244C>G",
          "hgvs_p": null,
          "transcript": "ENST00000482318.5",
          "protein_id": "ENSP00000477067.1",
          "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": 1710,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "n.*244C>G",
          "hgvs_p": null,
          "transcript": "ENST00000482318.5",
          "protein_id": "ENSP00000477067.1",
          "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": 1710,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.573C>G",
          "hgvs_p": "p.Ser191Arg",
          "transcript": "NM_001001890.3",
          "protein_id": "NP_001001890.1",
          "transcript_support_level": null,
          "aa_start": 191,
          "aa_end": null,
          "aa_length": 453,
          "cds_start": 573,
          "cds_end": null,
          "cds_length": 1362,
          "cdna_start": 2160,
          "cdna_end": null,
          "cdna_length": 7283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.618C>G",
          "hgvs_p": "p.Ser206Arg",
          "transcript": "ENST00000399237.6",
          "protein_id": "ENSP00000382182.2",
          "transcript_support_level": 5,
          "aa_start": 206,
          "aa_end": null,
          "aa_length": 255,
          "cds_start": 618,
          "cds_end": null,
          "cds_length": 769,
          "cdna_start": 671,
          "cdna_end": null,
          "cdna_length": 822,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.573C>G",
          "hgvs_p": "p.Ser191Arg",
          "transcript": "NM_001122607.2",
          "protein_id": "NP_001116079.1",
          "transcript_support_level": null,
          "aa_start": 191,
          "aa_end": null,
          "aa_length": 250,
          "cds_start": 573,
          "cds_end": null,
          "cds_length": 753,
          "cdna_start": 2160,
          "cdna_end": null,
          "cdna_length": 2729,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
          "hgvs_p": "p.Ser218Arg",
          "transcript": "XM_011529766.3",
          "protein_id": "XP_011528068.1",
          "transcript_support_level": null,
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          "cds_start": 654,
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          "cdna_start": 935,
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          "mane_select": null,
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        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
          "hgvs_p": "p.Ser218Arg",
          "transcript": "XM_047441007.1",
          "protein_id": "XP_047296963.1",
          "transcript_support_level": null,
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          "cdna_start": 1057,
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          "feature": null
        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.618C>G",
          "hgvs_p": "p.Ser206Arg",
          "transcript": "XM_005261068.4",
          "protein_id": "XP_005261125.1",
          "transcript_support_level": null,
          "aa_start": 206,
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          "cds_start": 618,
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          "cdna_start": 641,
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          "cdna_length": 5764,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
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          ],
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          "intron_rank": null,
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          "gene_symbol": "RUNX1",
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          "hgvs_c": "c.615C>G",
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        {
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          ],
          "exon_rank": 5,
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          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.615C>G",
          "hgvs_p": "p.Ser205Arg",
          "transcript": "XM_047441009.1",
          "protein_id": "XP_047296965.1",
          "transcript_support_level": null,
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          "cdna_start": 1018,
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        },
        {
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          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.615C>G",
          "hgvs_p": "p.Ser205Arg",
          "transcript": "XM_047441010.1",
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          "mane_select": null,
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        },
        {
          "aa_ref": "S",
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          "strand": false,
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          ],
          "exon_rank": 7,
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          "intron_rank": null,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.654C>G",
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        {
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          ],
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          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.532+24913C>G",
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        },
        {
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          ],
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          "exon_count": 8,
          "intron_rank": 6,
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          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.613+24913C>G",
          "hgvs_p": null,
          "transcript": "XM_005261069.5",
          "protein_id": "XP_005261126.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5779,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "RUNX1",
          "gene_hgnc_id": 10471,
          "hgvs_c": "c.613+24913C>G",
          "hgvs_p": null,
          "transcript": "XM_047441011.1",
          "protein_id": "XP_047296967.1",
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      "gnomad_exomes_af": null,
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      "phylop100way_prediction": "Uncertain_significance",
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      "acmg_by_gene": [
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          "verdict": "Uncertain_significance",
          "transcript": "NM_001754.5",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  ],
  "message": null
}