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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: 17-79047677-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=79047677&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 79047677,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_030968.5",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "NM_030968.5",
          "protein_id": "NP_112230.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000579760.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_030968.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000579760.6",
          "protein_id": "ENSP00000463922.1",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_030968.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000579760.6"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000580474.1",
          "protein_id": "ENSP00000463108.1",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000580474.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000581774.5",
          "protein_id": "ENSP00000462481.2",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000581774.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "NM_153372.3",
          "protein_id": "NP_699203.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_153372.3"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "NM_198593.4",
          "protein_id": "NP_940995.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_198593.4"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000339142.6",
          "protein_id": "ENSP00000340864.2",
          "transcript_support_level": 5,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000339142.6"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000354124.7",
          "protein_id": "ENSP00000343230.4",
          "transcript_support_level": 4,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000354124.7"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000392445.6",
          "protein_id": "ENSP00000376240.2",
          "transcript_support_level": 2,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000392445.6"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000580454.5",
          "protein_id": "ENSP00000462990.1",
          "transcript_support_level": 5,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000580454.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000583904.5",
          "protein_id": "ENSP00000463008.1",
          "transcript_support_level": 4,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000583904.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885300.1",
          "protein_id": "ENSP00000555359.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885300.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885301.1",
          "protein_id": "ENSP00000555360.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885301.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885302.1",
          "protein_id": "ENSP00000555361.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885303.1",
          "protein_id": "ENSP00000555362.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885303.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885304.1",
          "protein_id": "ENSP00000555363.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
          "cds_end": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000885304.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885305.1",
          "protein_id": "ENSP00000555364.1",
          "transcript_support_level": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885306.1",
          "protein_id": "ENSP00000555365.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000885306.1"
        },
        {
          "aa_ref": "Y",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
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          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885307.1",
          "protein_id": "ENSP00000555366.1",
          "transcript_support_level": null,
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          "cds_start": 435,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000885307.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr",
          "transcript": "ENST00000885308.1",
          "protein_id": "ENSP00000555367.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 435,
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          "cds_length": 846,
          "cdna_start": null,
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          "cdna_length": null,
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          "cds_start": 435,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047435297.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "c.189C>T",
          "hgvs_p": "p.Tyr63Tyr",
          "transcript": "XM_017024126.1",
          "protein_id": "XP_016879615.1",
          "transcript_support_level": null,
          "aa_start": 63,
          "aa_end": null,
          "aa_length": 199,
          "cds_start": 189,
          "cds_end": null,
          "cds_length": 600,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_017024126.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "n.449C>T",
          "hgvs_p": null,
          "transcript": "ENST00000582625.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": "pseudogene",
          "feature": "ENST00000582625.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "C1QTNF1",
          "gene_hgnc_id": 14324,
          "hgvs_c": "n.760C>T",
          "hgvs_p": null,
          "transcript": "NR_049769.3",
          "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": "pseudogene",
          "feature": "NR_049769.3"
        }
      ],
      "gene_symbol": "C1QTNF1",
      "gene_hgnc_id": 14324,
      "dbsnp": "rs34874100",
      "frequency_reference_population": 0.005149465,
      "hom_count_reference_population": 386,
      "allele_count_reference_population": 8311,
      "gnomad_exomes_af": 0.00284739,
      "gnomad_genomes_af": 0.0272491,
      "gnomad_exomes_ac": 4162,
      "gnomad_genomes_ac": 4149,
      "gnomad_exomes_homalt": 178,
      "gnomad_genomes_homalt": 208,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.46000000834465027,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.019999999552965164,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.46,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.362,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.02,
      "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": -19,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -19,
          "benign_score": 19,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_030968.5",
          "gene_symbol": "C1QTNF1",
          "hgnc_id": 14324,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Tyr145Tyr"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}