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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: 2-85848001-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=85848001&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 85848001,
      "ref": "G",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000638572.2",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.522C>G",
          "hgvs_p": "p.Leu174Leu",
          "transcript": "NM_003896.4",
          "protein_id": "NP_003887.3",
          "transcript_support_level": null,
          "aa_start": 174,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 522,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 607,
          "cdna_end": null,
          "cdna_length": 4366,
          "mane_select": "ENST00000638572.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.522C>G",
          "hgvs_p": "p.Leu174Leu",
          "transcript": "ENST00000638572.2",
          "protein_id": "ENSP00000491316.1",
          "transcript_support_level": 1,
          "aa_start": 174,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 522,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 607,
          "cdna_end": null,
          "cdna_length": 4366,
          "mane_select": "NM_003896.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.453C>G",
          "hgvs_p": "p.Leu151Leu",
          "transcript": "ENST00000393808.8",
          "protein_id": "ENSP00000377397.3",
          "transcript_support_level": 1,
          "aa_start": 151,
          "aa_end": null,
          "aa_length": 395,
          "cds_start": 453,
          "cds_end": null,
          "cds_length": 1188,
          "cdna_start": 506,
          "cdna_end": null,
          "cdna_length": 2236,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000393805.6",
          "protein_id": "ENSP00000377394.1",
          "transcript_support_level": 1,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 614,
          "cdna_end": null,
          "cdna_length": 2344,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "n.1576C>G",
          "hgvs_p": null,
          "transcript": "ENST00000461206.1",
          "protein_id": null,
          "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": 3487,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "n.*686C>G",
          "hgvs_p": null,
          "transcript": "ENST00000640378.1",
          "protein_id": "ENSP00000492030.1",
          "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": 2407,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "n.*686C>G",
          "hgvs_p": null,
          "transcript": "ENST00000640378.1",
          "protein_id": "ENSP00000492030.1",
          "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": 2407,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "5_prime_UTR_premature_start_codon_gain_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.-383C>G",
          "hgvs_p": null,
          "transcript": "NM_001354247.1",
          "protein_id": "NP_001341176.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 177,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 534,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4064,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.579C>G",
          "hgvs_p": "p.Leu193Leu",
          "transcript": "ENST00000640418.1",
          "protein_id": "ENSP00000492098.1",
          "transcript_support_level": 5,
          "aa_start": 193,
          "aa_end": null,
          "aa_length": 437,
          "cds_start": 579,
          "cds_end": null,
          "cds_length": 1314,
          "cdna_start": 776,
          "cdna_end": null,
          "cdna_length": 2467,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.519C>G",
          "hgvs_p": "p.Leu173Leu",
          "transcript": "ENST00000639305.1",
          "protein_id": "ENSP00000492244.1",
          "transcript_support_level": 5,
          "aa_start": 173,
          "aa_end": null,
          "aa_length": 406,
          "cds_start": 519,
          "cds_end": null,
          "cds_length": 1221,
          "cdna_start": 520,
          "cdna_end": null,
          "cdna_length": 2160,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.453C>G",
          "hgvs_p": "p.Leu151Leu",
          "transcript": "NM_001042437.2",
          "protein_id": "NP_001035902.1",
          "transcript_support_level": null,
          "aa_start": 151,
          "aa_end": null,
          "aa_length": 395,
          "cds_start": 453,
          "cds_end": null,
          "cds_length": 1188,
          "cdna_start": 506,
          "cdna_end": null,
          "cdna_length": 4265,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "NM_001354227.2",
          "protein_id": "NP_001341156.1",
          "transcript_support_level": null,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 794,
          "cdna_end": null,
          "cdna_length": 4553,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "NM_001354229.2",
          "protein_id": "NP_001341158.1",
          "transcript_support_level": null,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 738,
          "cdna_end": null,
          "cdna_length": 4497,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "NM_001354238.1",
          "protein_id": "NP_001341167.1",
          "transcript_support_level": null,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 583,
          "cdna_end": null,
          "cdna_length": 2329,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000638986.1",
          "protein_id": "ENSP00000491853.1",
          "transcript_support_level": 5,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 658,
          "cdna_end": null,
          "cdna_length": 2331,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000639432.1",
          "protein_id": "ENSP00000491828.1",
          "transcript_support_level": 5,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 614,
          "cdna_end": null,
          "cdna_length": 2297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000640322.1",
          "protein_id": "ENSP00000491564.1",
          "transcript_support_level": 5,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 639,
          "cdna_end": null,
          "cdna_length": 2368,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000640982.1",
          "protein_id": "ENSP00000492299.1",
          "transcript_support_level": 5,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 782,
          "cdna_end": null,
          "cdna_length": 2465,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.438C>G",
          "hgvs_p": "p.Leu146Leu",
          "transcript": "ENST00000640992.1",
          "protein_id": "ENSP00000492753.1",
          "transcript_support_level": 5,
          "aa_start": 146,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 438,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 609,
          "cdna_end": null,
          "cdna_length": 2292,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "c.402C>G",
          "hgvs_p": "p.Leu134Leu",
          "transcript": "ENST00000377332.8",
          "protein_id": "ENSP00000366549.4",
          "transcript_support_level": 5,
          "aa_start": 134,
          "aa_end": null,
          "aa_length": 378,
          "cds_start": 402,
          "cds_end": null,
          "cds_length": 1137,
          "cdna_start": 455,
          "cdna_end": null,
          "cdna_length": 2165,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "n.*210C>G",
          "hgvs_p": null,
          "transcript": "XR_007084231.1",
          "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": 1290,
          "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": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ST3GAL5",
          "gene_hgnc_id": 10872,
          "hgvs_c": "n.*210C>G",
          "hgvs_p": null,
          "transcript": "XR_007084237.1",
          "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": 1257,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ST3GAL5",
      "gene_hgnc_id": 10872,
      "dbsnp": "rs766829186",
      "frequency_reference_population": 0.000012996838,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 19,
      "gnomad_exomes_af": 0.0000129968,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 19,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8399999737739563,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": 0.2492,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.84,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.016,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -7,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -7,
          "benign_score": 7,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000638572.2",
          "gene_symbol": "ST3GAL5",
          "hgnc_id": 10872,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.522C>G",
          "hgvs_p": "p.Leu174Leu"
        }
      ],
      "clinvar_disease": "GM3 synthase deficiency",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "GM3 synthase deficiency",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}