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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: 2-47798639-GTGAAGAAGATAA-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=47798639&ref=GTGAAGAAGATAA&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 47798639,
      "ref": "GTGAAGAAGATAA",
      "alt": "G",
      "effect": "conservative_inframe_deletion",
      "transcript": "NM_000179.3",
      "consequences": [
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "NM_000179.3",
          "protein_id": "NP_000170.1",
          "transcript_support_level": null,
          "aa_start": 221,
          "aa_end": null,
          "aa_length": 1360,
          "cds_start": 661,
          "cds_end": null,
          "cds_length": 4083,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 4265,
          "mane_select": "ENST00000234420.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "ENST00000234420.11",
          "protein_id": "ENSP00000234420.5",
          "transcript_support_level": 1,
          "aa_start": 221,
          "aa_end": null,
          "aa_length": 1360,
          "cds_start": 661,
          "cds_end": null,
          "cds_length": 4083,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 4265,
          "mane_select": "NM_000179.3",
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "n.*8_*19delGAAGATAATGAA",
          "hgvs_p": null,
          "transcript": "ENST00000445503.5",
          "protein_id": "ENSP00000405294.1",
          "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": 4158,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "n.*8_*19delGAAGATAATGAA",
          "hgvs_p": null,
          "transcript": "ENST00000445503.5",
          "protein_id": "ENSP00000405294.1",
          "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": 4158,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.757_768delGAAGATAATGAA",
          "hgvs_p": "p.Glu253_Glu256del",
          "transcript": "NM_001406795.1",
          "protein_id": "NP_001393724.1",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 1392,
          "cds_start": 757,
          "cds_end": null,
          "cds_length": 4179,
          "cdna_start": 846,
          "cdna_end": null,
          "cdna_length": 4361,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.667_678delGAAGATAATGAA",
          "hgvs_p": "p.Glu223_Glu226del",
          "transcript": "NM_001406813.1",
          "protein_id": "NP_001393742.1",
          "transcript_support_level": null,
          "aa_start": 223,
          "aa_end": null,
          "aa_length": 1362,
          "cds_start": 667,
          "cds_end": null,
          "cds_length": 4089,
          "cdna_start": 756,
          "cdna_end": null,
          "cdna_length": 4271,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.667_678delGAAGATAATGAA",
          "hgvs_p": "p.Glu223_Glu226del",
          "transcript": "ENST00000700002.1",
          "protein_id": "ENSP00000514750.1",
          "transcript_support_level": null,
          "aa_start": 223,
          "aa_end": null,
          "aa_length": 1362,
          "cds_start": 667,
          "cds_end": null,
          "cds_length": 4089,
          "cdna_start": 739,
          "cdna_end": null,
          "cdna_length": 4233,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "NM_001406796.1",
          "protein_id": "NP_001393725.1",
          "transcript_support_level": null,
          "aa_start": 221,
          "aa_end": null,
          "aa_length": 1360,
          "cds_start": 661,
          "cds_end": null,
          "cds_length": 4083,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 4315,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "NM_001406809.1",
          "protein_id": "NP_001393738.1",
          "transcript_support_level": null,
          "aa_start": 221,
          "aa_end": null,
          "aa_length": 1360,
          "cds_start": 661,
          "cds_end": null,
          "cds_length": 4083,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 4318,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "EDNE",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "NM_001406808.1",
          "protein_id": "NP_001393737.1",
          "transcript_support_level": null,
          "aa_start": 221,
          "aa_end": null,
          "aa_length": 1337,
          "cds_start": 661,
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          "cds_length": 4014,
          "cdna_start": 750,
          "cdna_end": null,
          "cdna_length": 4260,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.583_594delGAAGATAATGAA",
          "hgvs_p": "p.Glu195_Glu198del",
          "transcript": "NM_001406804.1",
          "protein_id": "NP_001393733.1",
          "transcript_support_level": null,
          "aa_start": 195,
          "aa_end": null,
          "aa_length": 1334,
          "cds_start": 583,
          "cds_end": null,
          "cds_length": 4005,
          "cdna_start": 727,
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          "cdna_length": 4242,
          "mane_select": null,
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        {
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          "canonical": false,
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
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          "intron_rank": null,
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          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del",
          "transcript": "NM_001406800.1",
          "protein_id": "NP_001393729.1",
          "transcript_support_level": null,
          "aa_start": 221,
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          "cds_start": 661,
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          "cdna_start": 750,
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        {
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.757_768delGAAGATAATGAA",
          "hgvs_p": "p.Glu253_Glu256del",
          "transcript": "NM_001406802.1",
          "protein_id": "NP_001393731.1",
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.493_504delGAAGATAATGAA",
          "hgvs_p": "p.Glu165_Glu168del",
          "transcript": "NM_001406826.1",
          "protein_id": "NP_001393755.1",
          "transcript_support_level": null,
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          "aa_end": null,
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          "cds_start": 493,
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        {
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          ],
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          "gene_symbol": "MSH6",
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          "hgvs_c": "c.661_672delGAAGATAATGAA",
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          "transcript": "NM_001406798.1",
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        },
        {
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.364_375delGAAGATAATGAA",
          "hgvs_p": "p.Glu122_Glu125del",
          "transcript": "NM_001406797.1",
          "protein_id": "NP_001393726.1",
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        },
        {
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          ],
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.364_375delGAAGATAATGAA",
          "hgvs_p": "p.Glu122_Glu125del",
          "transcript": "NM_001406805.1",
          "protein_id": "NP_001393734.1",
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        {
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          "transcript": "NM_001406818.1",
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        {
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          ],
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          "hgvs_c": "c.364_375delGAAGATAATGAA",
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          "transcript": "NM_001406819.1",
          "protein_id": "NP_001393748.1",
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        },
        {
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          "consequences": [
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          ],
          "exon_rank": 4,
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          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "c.364_375delGAAGATAATGAA",
          "hgvs_p": "p.Glu122_Glu125del",
          "transcript": "NM_001406820.1",
          "protein_id": "NP_001393749.1",
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          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "n.627+2581_627+2592delGAAGATAATGAA",
          "hgvs_p": null,
          "transcript": "ENST00000700003.1",
          "protein_id": "ENSP00000514751.1",
          "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": 1593,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "n.717-1194_717-1183delGAAGATAATGAA",
          "hgvs_p": null,
          "transcript": "NR_176256.1",
          "protein_id": null,
          "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": 3106,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MSH6",
          "gene_hgnc_id": 7329,
          "hgvs_c": "n.*217_*228delTGAAGAAGATAA",
          "hgvs_p": null,
          "transcript": "ENST00000700001.1",
          "protein_id": null,
          "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": 3059,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MSH6",
      "gene_hgnc_id": 7329,
      "dbsnp": "rs1553412079",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "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": 7.02,
      "phylop100way_prediction": "Uncertain_significance",
      "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": "Uncertain_significance",
      "acmg_criteria": "PM4",
      "acmg_by_gene": [
        {
          "score": 2,
          "benign_score": 0,
          "pathogenic_score": 2,
          "criteria": [
            "PM4"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_000179.3",
          "gene_symbol": "MSH6",
          "hgnc_id": 7329,
          "effects": [
            "conservative_inframe_deletion"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.661_672delGAAGATAATGAA",
          "hgvs_p": "p.Glu221_Glu224del"
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000434234.5",
          "gene_symbol": "FBXO11",
          "hgnc_id": 13590,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "n.*125-9211_*125-9200delTTATCTTCTTCA",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Hereditary cancer-predisposing syndrome,Hereditary nonpolyposis colorectal neoplasms,not provided,not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:5",
      "phenotype_combined": "Hereditary nonpolyposis colorectal neoplasms|Hereditary cancer-predisposing syndrome|not specified|not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}