← 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: X-5892907-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=5892907&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 5892907,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000381095.8",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_181332.3",
          "protein_id": "NP_851849.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2993,
          "cdna_end": null,
          "cdna_length": 5858,
          "mane_select": "ENST00000381095.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "ENST00000381095.8",
          "protein_id": "ENSP00000370485.3",
          "transcript_support_level": 1,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2993,
          "cdna_end": null,
          "cdna_length": 5858,
          "mane_select": "NM_181332.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "ENST00000538097.6",
          "protein_id": "ENSP00000439203.3",
          "transcript_support_level": 1,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 2421,
          "cdna_end": null,
          "cdna_length": 3124,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "ENST00000275857.10",
          "protein_id": "ENSP00000275857.6",
          "transcript_support_level": 1,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2825,
          "cdna_end": null,
          "cdna_length": 5454,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001282145.2",
          "protein_id": "NP_001269074.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3300,
          "cdna_end": null,
          "cdna_length": 6165,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001282146.2",
          "protein_id": "NP_001269075.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2874,
          "cdna_end": null,
          "cdna_length": 5739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001441322.1",
          "protein_id": "NP_001428251.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2888,
          "cdna_end": null,
          "cdna_length": 5753,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001441323.1",
          "protein_id": "NP_001428252.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2736,
          "cdna_end": null,
          "cdna_length": 5601,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001441324.1",
          "protein_id": "NP_001428253.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3061,
          "cdna_end": null,
          "cdna_length": 5926,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_001441325.1",
          "protein_id": "NP_001428254.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3066,
          "cdna_end": null,
          "cdna_length": 5931,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "NM_020742.4",
          "protein_id": "NP_065793.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2825,
          "cdna_end": null,
          "cdna_length": 5690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "ENST00000381092.1",
          "protein_id": "ENSP00000370482.1",
          "transcript_support_level": 2,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3048,
          "cdna_end": null,
          "cdna_length": 3750,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "ENST00000381093.6",
          "protein_id": "ENSP00000370483.3",
          "transcript_support_level": 2,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2990,
          "cdna_end": null,
          "cdna_length": 5865,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_005274564.4",
          "protein_id": "XP_005274621.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 3053,
          "cdna_end": null,
          "cdna_length": 5918,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_005274565.3",
          "protein_id": "XP_005274622.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 2934,
          "cdna_end": null,
          "cdna_length": 5799,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_005274566.5",
          "protein_id": "XP_005274623.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 2796,
          "cdna_end": null,
          "cdna_length": 5661,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_006724504.3",
          "protein_id": "XP_006724567.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 2930,
          "cdna_end": null,
          "cdna_length": 5795,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_011545547.3",
          "protein_id": "XP_011543849.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 2948,
          "cdna_end": null,
          "cdna_length": 5813,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2421G>A",
          "hgvs_p": "p.Thr807Thr",
          "transcript": "XM_011545548.3",
          "protein_id": "XP_011543850.1",
          "transcript_support_level": null,
          "aa_start": 807,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 2421,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 3178,
          "cdna_end": null,
          "cdna_length": 6043,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "XM_017029693.2",
          "protein_id": "XP_016885182.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3116,
          "cdna_end": null,
          "cdna_length": 5981,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "XM_047442281.1",
          "protein_id": "XP_047298237.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 3115,
          "cdna_end": null,
          "cdna_length": 5980,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr",
          "transcript": "XM_047442282.1",
          "protein_id": "XP_047298238.1",
          "transcript_support_level": null,
          "aa_start": 787,
          "aa_end": null,
          "aa_length": 816,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": 2961,
          "cdna_end": null,
          "cdna_length": 5826,
          "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": "NLGN4X",
          "gene_hgnc_id": 14287,
          "hgvs_c": "n.277+10170G>A",
          "hgvs_p": null,
          "transcript": "ENST00000477079.1",
          "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": 600,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "NLGN4X",
      "gene_hgnc_id": 14287,
      "dbsnp": "rs374449420",
      "frequency_reference_population": 0.000009097849,
      "hom_count_reference_population": 6,
      "allele_count_reference_population": 11,
      "gnomad_exomes_af": 0.00000910539,
      "gnomad_genomes_af": 0.00000902307,
      "gnomad_exomes_ac": 10,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.4399999976158142,
      "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": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.44,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.094,
      "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_Moderate,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -7,
          "benign_score": 7,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000381095.8",
          "gene_symbol": "NLGN4X",
          "hgnc_id": 14287,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.2361G>A",
          "hgvs_p": "p.Thr787Thr"
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}