← Back to variant description

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: 8-1763857-GCAGGGAGCCCGGCTGAGTGGCAGCCCAGGTGAGCGCT-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=1763857&ref=GCAGGGAGCCCGGCTGAGTGGCAGCCCAGGTGAGCGCT&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 1763857,
      "ref": "GCAGGGAGCCCGGCTGAGTGGCAGCCCAGGTGAGCGCT",
      "alt": "G",
      "effect": "splice_donor_variant,splice_region_variant,5_prime_UTR_variant,intron_variant",
      "transcript": "NM_018941.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "NM_018941.4",
          "protein_id": "NP_061764.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "ENST00000331222.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000331222.6",
          "protein_id": "ENSP00000328182.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "NM_018941.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KBTBD11-OT1",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-195_-159delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635855.1",
          "protein_id": "ENSP00000489726.1",
          "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": 6169,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KBTBD11-OT1",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-195_-159delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635855.1",
          "protein_id": "ENSP00000489726.1",
          "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": 6169,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "NM_018941.4",
          "protein_id": "NP_061764.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "ENST00000331222.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000331222.6",
          "protein_id": "ENSP00000328182.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "NM_018941.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "NM_018941.4",
          "protein_id": "NP_061764.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "ENST00000331222.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000331222.6",
          "protein_id": "ENSP00000328182.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7084,
          "mane_select": "NM_018941.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": null,
          "protein_coding": null,
          "strand": true,
          "consequences": [
            "gene_fusion"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "n.1763858_1763894delCAGGGAGCCCGGCTGAGTGGCAGCCCAGGTGAGCGCT",
          "hgvs_p": null,
          "transcript": null,
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": null,
          "protein_coding": null,
          "strand": false,
          "consequences": [
            "bidirectional_gene_fusion"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.1763894_1763858delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": null,
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-295_-280+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637083.1",
          "protein_id": "ENSP00000490235.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000520991.3",
          "protein_id": "ENSP00000487905.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636934.1",
          "protein_id": "ENSP00000490218.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1790,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_011534747.3",
          "protein_id": "XP_011533049.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 263,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 792,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3036,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "n.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635970.1",
          "protein_id": "ENSP00000490439.1",
          "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": 1958,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-195_-159delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635751.1",
          "protein_id": "ENSP00000489694.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1807,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-179_-143delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637156.1",
          "protein_id": "ENSP00000490458.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1897,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-179_-143delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_005266021.5",
          "protein_id": "XP_005266078.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7124,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-195_-159delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_011534745.2",
          "protein_id": "XP_011533047.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7140,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-252_-216delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_011534746.3",
          "protein_id": "XP_011533048.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7197,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-179_-143delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_047421513.1",
          "protein_id": "XP_047277469.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 263,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 792,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3076,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-124+59_-124+95delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000519254.2",
          "protein_id": "ENSP00000490016.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1769,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-295_-280+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637083.1",
          "protein_id": "ENSP00000490235.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000520991.3",
          "protein_id": "ENSP00000487905.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636934.1",
          "protein_id": "ENSP00000490218.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1790,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-123-7062_-123-7026delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000524258.2",
          "protein_id": "ENSP00000488898.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 134,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 835,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.69+540_69+576delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000517959.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 917,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.139+407_139+443delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000518822.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 1078,
          "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_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "n.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635970.1",
          "protein_id": "ENSP00000490439.1",
          "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": 1958,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.230+540_230+576delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000659375.2",
          "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": 2095,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.189+540_189+576delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000727631.1",
          "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": 900,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.155+540_155+576delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000727632.1",
          "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": 694,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.122+407_122+443delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "ENST00000727636.1",
          "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": 595,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8-AS1",
          "gene_hgnc_id": 55523,
          "hgvs_c": "n.151+540_151+576delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null,
          "transcript": "NR_134303.1",
          "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": 1117,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-123-7062_-123-7026delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_005266022.2",
          "protein_id": "XP_005266079.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7314,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-124+59_-124+95delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_005266023.2",
          "protein_id": "XP_005266080.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7106,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-123-7062_-123-7026delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_047421512.1",
          "protein_id": "XP_047277468.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7126,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_011534747.3",
          "protein_id": "XP_011533049.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 263,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 792,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3036,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-295_-280+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637083.1",
          "protein_id": "ENSP00000490235.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000520991.3",
          "protein_id": "ENSP00000487905.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636934.1",
          "protein_id": "ENSP00000490218.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1790,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN8",
          "gene_hgnc_id": 2079,
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null,
          "transcript": "XM_011534747.3",
          "protein_id": "XP_011533049.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 263,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 792,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3036,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KBTBD11-OT1",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-207_-171delCAGGGAGCCCGGCTGAGTGGCAGCCCAGGTGAGCGCT",
          "hgvs_p": null,
          "transcript": "ENST00000635855.1",
          "protein_id": "ENSP00000489726.1",
          "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": 6169,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CLN8",
      "gene_hgnc_id": 2079,
      "dbsnp": "rs1064796355",
      "frequency_reference_population": 0.0000066133193,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000661332,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "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": 1.608,
      "phylop100way_prediction": "Benign",
      "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": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Strong",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PVS1_Strong"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_018941.4",
          "gene_symbol": "CLN8",
          "hgnc_id": 2079,
          "effects": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.-139_-124+21delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000635855.1",
          "gene_symbol": "KBTBD11-OT1",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-195_-159delCTGAGTGGCAGCCCAGGTGAGCGCTCAGGGAGCCCGG",
          "hgvs_p": null
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "",
          "gene_symbol": "CLN8-AS1",
          "hgnc_id": 55523,
          "effects": [
            "bidirectional_gene_fusion"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.1763894_1763858delAGCGCTCACCTGGGCTGCCACTCAGCCGGGCTCCCTG",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}