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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: 12-64495483-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=64495483&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 64495483,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant,splice_region_variant",
      "transcript": "ENST00000331710.10",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "NM_013254.4",
          "protein_id": "NP_037386.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 1621,
          "cdna_end": null,
          "cdna_length": 3022,
          "mane_select": "ENST00000331710.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "ENST00000331710.10",
          "protein_id": "ENSP00000329967.5",
          "transcript_support_level": 1,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 1621,
          "cdna_end": null,
          "cdna_length": 3022,
          "mane_select": "NM_013254.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "ENST00000650790.1",
          "protein_id": "ENSP00000498995.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 1664,
          "cdna_end": null,
          "cdna_length": 3006,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "ENST00000677641.1",
          "protein_id": "ENSP00000504637.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 728,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2187,
          "cdna_start": 1651,
          "cdna_end": null,
          "cdna_length": 3001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "ENST00000652657.1",
          "protein_id": "ENSP00000498887.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": 1629,
          "cdna_end": null,
          "cdna_length": 2944,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1420C>A",
          "hgvs_p": "p.Leu474Ile",
          "transcript": "ENST00000678180.1",
          "protein_id": "ENSP00000504132.1",
          "transcript_support_level": null,
          "aa_start": 474,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": 1420,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": 1516,
          "cdna_end": null,
          "cdna_length": 2869,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1366C>A",
          "hgvs_p": "p.Leu456Ile",
          "transcript": "ENST00000651014.1",
          "protein_id": "ENSP00000498885.1",
          "transcript_support_level": null,
          "aa_start": 456,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1366,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 1710,
          "cdna_end": null,
          "cdna_length": 3046,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1366C>A",
          "hgvs_p": "p.Leu456Ile",
          "transcript": "ENST00000676912.1",
          "protein_id": "ENSP00000503567.1",
          "transcript_support_level": null,
          "aa_start": 456,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1366,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 1569,
          "cdna_end": null,
          "cdna_length": 2956,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1264C>A",
          "hgvs_p": "p.Leu422Ile",
          "transcript": "ENST00000650762.1",
          "protein_id": "ENSP00000498758.1",
          "transcript_support_level": null,
          "aa_start": 422,
          "aa_end": null,
          "aa_length": 643,
          "cds_start": 1264,
          "cds_end": null,
          "cds_length": 1932,
          "cdna_start": 1431,
          "cdna_end": null,
          "cdna_length": 2459,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1174C>A",
          "hgvs_p": "p.Leu392Ile",
          "transcript": "ENST00000676930.1",
          "protein_id": "ENSP00000502899.1",
          "transcript_support_level": null,
          "aa_start": 392,
          "aa_end": null,
          "aa_length": 613,
          "cds_start": 1174,
          "cds_end": null,
          "cds_length": 1842,
          "cdna_start": 1262,
          "cdna_end": null,
          "cdna_length": 2649,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "XM_005268809.2",
          "protein_id": "XP_005268866.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 1829,
          "cdna_end": null,
          "cdna_length": 3230,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "c.1522C>A",
          "hgvs_p": "p.Leu508Ile",
          "transcript": "XM_005268810.2",
          "protein_id": "XP_005268867.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": 2072,
          "cdna_end": null,
          "cdna_length": 3473,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.555C>A",
          "hgvs_p": null,
          "transcript": "ENST00000541805.2",
          "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": 1380,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.428C>A",
          "hgvs_p": null,
          "transcript": "ENST00000545392.2",
          "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,
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          "cdna_length": 1781,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.1396C>A",
          "hgvs_p": null,
          "transcript": "ENST00000650708.1",
          "protein_id": "ENSP00000498667.1",
          "transcript_support_level": null,
          "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": 2751,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*1667C>A",
          "hgvs_p": null,
          "transcript": "ENST00000650786.1",
          "protein_id": "ENSP00000498280.1",
          "transcript_support_level": null,
          "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": 3244,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.1522C>A",
          "hgvs_p": null,
          "transcript": "ENST00000650997.1",
          "protein_id": "ENSP00000498341.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.1522C>A",
          "hgvs_p": null,
          "transcript": "ENST00000651262.1",
          "protein_id": "ENSP00000498461.1",
          "transcript_support_level": null,
          "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": 2902,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.*1006C>A",
          "hgvs_p": null,
          "transcript": "ENST00000651878.1",
          "protein_id": "ENSP00000499077.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3151,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TBK1",
          "gene_hgnc_id": 11584,
          "hgvs_c": "n.1522C>A",
          "hgvs_p": null,
          "transcript": "ENST00000652537.1",
          "protein_id": "ENSP00000499102.1",
          "transcript_support_level": null,
          "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": 3092,
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
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      "revel_prediction": "Benign",
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      "alphamissense_prediction": "Benign",
      "bayesdelnoaf_score": -0.42,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 4.487,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
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      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
      "acmg_by_gene": [
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          "verdict": "Benign",
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      "clinvar_disease": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 4,TBK1-related disorder,not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "Frontotemporal dementia and/or amyotrophic lateral sclerosis 4|TBK1-related disorder|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
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  ],
  "message": null
}