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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: 19-19193985-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=19193985&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 19193985,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_003721.4",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_003721.4",
          "protein_id": "NP_003712.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 260,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 783,
          "cdna_start": 485,
          "cdna_end": null,
          "cdna_length": 1376,
          "mane_select": "ENST00000303088.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000303088.9",
          "protein_id": "ENSP00000305071.2",
          "transcript_support_level": 1,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 260,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 783,
          "cdna_start": 485,
          "cdna_end": null,
          "cdna_length": 1376,
          "mane_select": "NM_003721.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000407360.7",
          "protein_id": "ENSP00000384572.3",
          "transcript_support_level": 1,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 260,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 783,
          "cdna_start": 385,
          "cdna_end": null,
          "cdna_length": 1212,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000456252.7",
          "protein_id": "ENSP00000409138.2",
          "transcript_support_level": 1,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 238,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 717,
          "cdna_start": 500,
          "cdna_end": null,
          "cdna_length": 1325,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000392324.8",
          "protein_id": "ENSP00000376138.3",
          "transcript_support_level": 1,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 237,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 714,
          "cdna_start": 237,
          "cdna_end": null,
          "cdna_length": 1059,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370238.1",
          "protein_id": "NP_001357167.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 285,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 858,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370237.1",
          "protein_id": "NP_001357166.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 284,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 855,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1176,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370233.1",
          "protein_id": "NP_001357162.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 260,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 783,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1104,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370235.1",
          "protein_id": "NP_001357164.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 259,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 780,
          "cdna_start": 464,
          "cdna_end": null,
          "cdna_length": 1352,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370236.1",
          "protein_id": "NP_001357165.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 259,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 780,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1101,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001278727.2",
          "protein_id": "NP_001265656.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 238,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 717,
          "cdna_start": 485,
          "cdna_end": null,
          "cdna_length": 1310,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001370234.1",
          "protein_id": "NP_001357163.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 238,
          "cds_start": 39,
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          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1038,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_001278728.2",
          "protein_id": "NP_001265657.1",
          "transcript_support_level": null,
          "aa_start": 13,
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          "cds_start": 39,
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          "cds_length": 714,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 1035,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "NM_134440.3",
          "protein_id": "NP_604389.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 237,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 714,
          "cdna_start": 485,
          "cdna_end": null,
          "cdna_length": 1307,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
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          "exon_count": 6,
          "intron_rank": null,
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          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000540981.5",
          "protein_id": "ENSP00000440325.2",
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          "cdna_start": 307,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000593273.5",
          "protein_id": "ENSP00000466913.1",
          "transcript_support_level": 3,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 144,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 435,
          "cdna_start": 469,
          "cdna_end": null,
          "cdna_length": 865,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "ENST00000421262.7",
          "protein_id": "ENSP00000393159.3",
          "transcript_support_level": 5,
          "aa_start": 13,
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          "aa_length": 82,
          "cds_start": 39,
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          "cds_length": 250,
          "cdna_start": 645,
          "cdna_end": null,
          "cdna_length": 856,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
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          "intron_rank": null,
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          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "XM_047439586.1",
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          "biotype": null,
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "XM_047439587.1",
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
          "hgvs_p": "p.Thr13Thr",
          "transcript": "XM_047439588.1",
          "protein_id": "XP_047295544.1",
          "transcript_support_level": null,
          "aa_start": 13,
          "aa_end": null,
          "aa_length": 285,
          "cds_start": 39,
          "cds_end": null,
          "cds_length": 858,
          "cdna_start": 207,
          "cdna_end": null,
          "cdna_length": 1173,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RFXANK",
          "gene_hgnc_id": 9987,
          "hgvs_c": "c.39C>A",
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      "gene_symbol": "RFXANK",
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      "dbsnp": "rs763281760",
      "frequency_reference_population": 0.0000074344653,
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      "allele_count_reference_population": 12,
      "gnomad_exomes_af": 0.00000410427,
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      "gnomad_exomes_ac": 6,
      "gnomad_genomes_ac": 6,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6700000166893005,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.67,
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      "phylop100way_score": 0.84,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "mitotip_score": null,
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      "acmg_score": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
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          "verdict": "Likely_benign",
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      "clinvar_disease": "MHC class II deficiency",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "MHC class II deficiency",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}