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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: 5-119525929-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=119525929&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 119525929,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000510025.7",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1586C>G",
          "hgvs_p": "p.Pro529Arg",
          "transcript": "NM_000414.4",
          "protein_id": "NP_000405.1",
          "transcript_support_level": null,
          "aa_start": 529,
          "aa_end": null,
          "aa_length": 736,
          "cds_start": 1586,
          "cds_end": null,
          "cds_length": 2211,
          "cdna_start": 1665,
          "cdna_end": null,
          "cdna_length": 2628,
          "mane_select": "ENST00000510025.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1586C>G",
          "hgvs_p": "p.Pro529Arg",
          "transcript": "ENST00000510025.7",
          "protein_id": "ENSP00000424940.3",
          "transcript_support_level": 2,
          "aa_start": 529,
          "aa_end": null,
          "aa_length": 736,
          "cds_start": 1586,
          "cds_end": null,
          "cds_length": 2211,
          "cdna_start": 1665,
          "cdna_end": null,
          "cdna_length": 2628,
          "mane_select": "NM_000414.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1517C>G",
          "hgvs_p": "p.Pro506Arg",
          "transcript": "ENST00000509514.6",
          "protein_id": "ENSP00000426272.2",
          "transcript_support_level": 1,
          "aa_start": 506,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 1517,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": 1617,
          "cdna_end": null,
          "cdna_length": 2566,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1661C>G",
          "hgvs_p": "p.Pro554Arg",
          "transcript": "NM_001199291.3",
          "protein_id": "NP_001186220.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 761,
          "cds_start": 1661,
          "cds_end": null,
          "cds_length": 2286,
          "cdna_start": 1918,
          "cdna_end": null,
          "cdna_length": 2881,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1661C>G",
          "hgvs_p": "p.Pro554Arg",
          "transcript": "ENST00000414835.7",
          "protein_id": "ENSP00000411960.3",
          "transcript_support_level": 2,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 761,
          "cds_start": 1661,
          "cds_end": null,
          "cds_length": 2286,
          "cdna_start": 1918,
          "cdna_end": null,
          "cdna_length": 2881,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1577C>G",
          "hgvs_p": "p.Pro526Arg",
          "transcript": "NM_001374497.1",
          "protein_id": "NP_001361426.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 733,
          "cds_start": 1577,
          "cds_end": null,
          "cds_length": 2202,
          "cdna_start": 1656,
          "cdna_end": null,
          "cdna_length": 2619,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1532C>G",
          "hgvs_p": "p.Pro511Arg",
          "transcript": "NM_001199292.2",
          "protein_id": "NP_001186221.1",
          "transcript_support_level": null,
          "aa_start": 511,
          "aa_end": null,
          "aa_length": 718,
          "cds_start": 1532,
          "cds_end": null,
          "cds_length": 2157,
          "cdna_start": 1611,
          "cdna_end": null,
          "cdna_length": 2574,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1532C>G",
          "hgvs_p": "p.Pro511Arg",
          "transcript": "ENST00000515320.5",
          "protein_id": "ENSP00000424613.1",
          "transcript_support_level": 2,
          "aa_start": 511,
          "aa_end": null,
          "aa_length": 718,
          "cds_start": 1532,
          "cds_end": null,
          "cds_length": 2157,
          "cdna_start": 1611,
          "cdna_end": null,
          "cdna_length": 2494,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1514C>G",
          "hgvs_p": "p.Pro505Arg",
          "transcript": "NM_001292027.2",
          "protein_id": "NP_001278956.1",
          "transcript_support_level": null,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 1514,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": 1730,
          "cdna_end": null,
          "cdna_length": 2693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1514C>G",
          "hgvs_p": "p.Pro505Arg",
          "transcript": "NM_001374498.1",
          "protein_id": "NP_001361427.1",
          "transcript_support_level": null,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 1514,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": 1593,
          "cdna_end": null,
          "cdna_length": 2556,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1514C>G",
          "hgvs_p": "p.Pro505Arg",
          "transcript": "ENST00000682996.1",
          "protein_id": "ENSP00000507792.1",
          "transcript_support_level": null,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 1514,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": 1614,
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          "cdna_length": 2563,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1586C>G",
          "hgvs_p": "p.Pro529Arg",
          "transcript": "ENST00000646058.1",
          "protein_id": "ENSP00000493579.1",
          "transcript_support_level": null,
          "aa_start": 529,
          "aa_end": null,
          "aa_length": 711,
          "cds_start": 1586,
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          "cdna_start": 1653,
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          "cdna_length": 2780,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
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          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1259C>G",
          "hgvs_p": "p.Pro420Arg",
          "transcript": "NM_001374499.1",
          "protein_id": "NP_001361428.1",
          "transcript_support_level": null,
          "aa_start": 420,
          "aa_end": null,
          "aa_length": 627,
          "cds_start": 1259,
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          "cds_length": 1884,
          "cdna_start": 1871,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1175C>G",
          "hgvs_p": "p.Pro392Arg",
          "transcript": "NM_001374501.1",
          "protein_id": "NP_001361430.1",
          "transcript_support_level": null,
          "aa_start": 392,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1175,
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          "cds_length": 1800,
          "cdna_start": 1853,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "P",
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          ],
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          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1175C>G",
          "hgvs_p": "p.Pro392Arg",
          "transcript": "NM_001374502.1",
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          "cds_start": 1175,
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          "cdna_start": 1858,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1175C>G",
          "hgvs_p": "p.Pro392Arg",
          "transcript": "NM_001374503.1",
          "protein_id": "NP_001361432.1",
          "transcript_support_level": null,
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          "aa_length": 599,
          "cds_start": 1175,
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          "cds_length": 1800,
          "cdna_start": 1923,
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          "cdna_length": 2886,
          "mane_select": null,
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        },
        {
          "aa_ref": "P",
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          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1175C>G",
          "hgvs_p": "p.Pro392Arg",
          "transcript": "ENST00000513628.5",
          "protein_id": "ENSP00000425993.1",
          "transcript_support_level": 2,
          "aa_start": 392,
          "aa_end": null,
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          "cds_start": 1175,
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          "cds_length": 1800,
          "cdna_start": 1420,
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        },
        {
          "aa_ref": "P",
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          ],
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          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1166C>G",
          "hgvs_p": "p.Pro389Arg",
          "transcript": "NM_001292028.2",
          "protein_id": "NP_001278957.1",
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        },
        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "HSD17B4",
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          "hgvs_p": "p.Pro382Arg",
          "transcript": "NM_001374500.1",
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          "feature": null
        },
        {
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          "strand": true,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HSD17B4",
          "gene_hgnc_id": 5213,
          "hgvs_c": "c.1145C>G",
          "hgvs_p": "p.Pro382Arg",
          "transcript": "ENST00000645099.1",
          "protein_id": "ENSP00000496091.1",
          "transcript_support_level": null,
          "aa_start": 382,
          "aa_end": null,
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          "cds_start": 1145,
          "cds_end": null,
          "cds_length": 1770,
          "cdna_start": 1480,
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          "cdna_length": 2112,
          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "P",
          "aa_alt": "R",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
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        {
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        {
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          "transcript": "ENST00000684160.1",
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      ],
      "gene_symbol": "HSD17B4",
      "gene_hgnc_id": 5213,
      "dbsnp": "rs1554068269",
      "frequency_reference_population": 0.0000013788767,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": 0.00000137888,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.9865055084228516,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.92,
      "revel_prediction": "Pathogenic",
      "alphamissense_score": 0.9337,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.36,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 6.835,
      "phylop100way_prediction": "Uncertain_significance",
      "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": 8,
      "acmg_classification": "Likely_pathogenic",
      "acmg_criteria": "PM1,PM2,PP3_Strong",
      "acmg_by_gene": [
        {
          "score": 8,
          "benign_score": 0,
          "pathogenic_score": 8,
          "criteria": [
            "PM1",
            "PM2",
            "PP3_Strong"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000510025.7",
          "gene_symbol": "HSD17B4",
          "hgnc_id": 5213,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1586C>G",
          "hgvs_p": "p.Pro529Arg"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}