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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: 12-132632318-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=132632318&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 132632318,
      "ref": "G",
      "alt": "T",
      "effect": "stop_gained",
      "transcript": "ENST00000320574.10",
      "consequences": [
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.6327C>A",
          "hgvs_p": "p.Cys2109*",
          "transcript": "NM_006231.4",
          "protein_id": "NP_006222.2",
          "transcript_support_level": null,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2286,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6861,
          "cdna_start": 6354,
          "cdna_end": null,
          "cdna_length": 7823,
          "mane_select": "ENST00000320574.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.6327C>A",
          "hgvs_p": "p.Cys2109*",
          "transcript": "ENST00000320574.10",
          "protein_id": "ENSP00000322570.5",
          "transcript_support_level": 1,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2286,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6861,
          "cdna_start": 6354,
          "cdna_end": null,
          "cdna_length": 7823,
          "mane_select": "NM_006231.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.6246C>A",
          "hgvs_p": "p.Cys2082*",
          "transcript": "ENST00000535270.5",
          "protein_id": "ENSP00000445753.1",
          "transcript_support_level": 1,
          "aa_start": 2082,
          "aa_end": null,
          "aa_length": 2259,
          "cds_start": 6246,
          "cds_end": null,
          "cds_length": 6780,
          "cdna_start": 6259,
          "cdna_end": null,
          "cdna_length": 6800,
          "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": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*6078C>A",
          "hgvs_p": null,
          "transcript": "ENST00000537064.5",
          "protein_id": "ENSP00000442578.1",
          "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": 8011,
          "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": 45,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*6078C>A",
          "hgvs_p": null,
          "transcript": "ENST00000537064.5",
          "protein_id": "ENSP00000442578.1",
          "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": 8011,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.6327C>A",
          "hgvs_p": "p.Cys2109*",
          "transcript": "XM_011534795.4",
          "protein_id": "XP_011533097.1",
          "transcript_support_level": null,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2298,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6897,
          "cdna_start": 6354,
          "cdna_end": null,
          "cdna_length": 7087,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.5406C>A",
          "hgvs_p": "p.Cys1802*",
          "transcript": "XM_011534797.4",
          "protein_id": "XP_011533099.1",
          "transcript_support_level": null,
          "aa_start": 1802,
          "aa_end": null,
          "aa_length": 1991,
          "cds_start": 5406,
          "cds_end": null,
          "cds_length": 5976,
          "cdna_start": 5500,
          "cdna_end": null,
          "cdna_length": 6233,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "c.3315C>A",
          "hgvs_p": "p.Cys1105*",
          "transcript": "XM_011534802.4",
          "protein_id": "XP_011533104.1",
          "transcript_support_level": null,
          "aa_start": 1105,
          "aa_end": null,
          "aa_length": 1294,
          "cds_start": 3315,
          "cds_end": null,
          "cds_length": 3885,
          "cdna_start": 3353,
          "cdna_end": null,
          "cdna_length": 4087,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*1499C>A",
          "hgvs_p": null,
          "transcript": "ENST00000434528.5",
          "protein_id": "ENSP00000500921.1",
          "transcript_support_level": 5,
          "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": 2406,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*82C>A",
          "hgvs_p": null,
          "transcript": "ENST00000441786.3",
          "protein_id": "ENSP00000480727.1",
          "transcript_support_level": 5,
          "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": 556,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.240C>A",
          "hgvs_p": null,
          "transcript": "ENST00000534922.6",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 567,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.99C>A",
          "hgvs_p": null,
          "transcript": "ENST00000538196.1",
          "protein_id": null,
          "transcript_support_level": 4,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 551,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*3053C>A",
          "hgvs_p": null,
          "transcript": "ENST00000544870.6",
          "protein_id": "ENSP00000479927.2",
          "transcript_support_level": 3,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5435,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*3073C>A",
          "hgvs_p": null,
          "transcript": "ENST00000672002.1",
          "protein_id": "ENSP00000500233.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 5455,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 50,
          "intron_rank": null,
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          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*6533C>A",
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          "transcript": "ENST00000672742.1",
          "protein_id": "ENSP00000500279.1",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.3981C>A",
          "hgvs_p": null,
          "transcript": "ENST00000699981.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5450,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*5297C>A",
          "hgvs_p": null,
          "transcript": "ENST00000699982.1",
          "protein_id": "ENSP00000514736.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 7636,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*6001C>A",
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          "transcript": "ENST00000699983.1",
          "protein_id": "ENSP00000514737.1",
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          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*5229C>A",
          "hgvs_p": null,
          "transcript": "ENST00000699984.1",
          "protein_id": "ENSP00000514738.1",
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          "cdna_start": null,
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          "cdna_length": 7561,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*1499C>A",
          "hgvs_p": null,
          "transcript": "ENST00000434528.5",
          "protein_id": "ENSP00000500921.1",
          "transcript_support_level": 5,
          "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": 2406,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POLE",
          "gene_hgnc_id": 9177,
          "hgvs_c": "n.*82C>A",
          "hgvs_p": null,
          "transcript": "ENST00000441786.3",
          "protein_id": "ENSP00000480727.1",
          "transcript_support_level": 5,
          "aa_start": null,
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
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      "custom_annotations": null
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  "message": null
}