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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: 14-102041574-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=102041574&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 102041574,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant,splice_region_variant",
      "transcript": "ENST00000360184.10",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg",
          "transcript": "NM_001376.5",
          "protein_id": "NP_001367.2",
          "transcript_support_level": null,
          "aa_start": 3981,
          "aa_end": null,
          "aa_length": 4646,
          "cds_start": 11942,
          "cds_end": null,
          "cds_length": 13941,
          "cdna_start": 12061,
          "cdna_end": null,
          "cdna_length": 19940,
          "mane_select": "ENST00000360184.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg",
          "transcript": "ENST00000360184.10",
          "protein_id": "ENSP00000348965.4",
          "transcript_support_level": 1,
          "aa_start": 3981,
          "aa_end": null,
          "aa_length": 4646,
          "cds_start": 11942,
          "cds_end": null,
          "cds_length": 13941,
          "cdna_start": 12061,
          "cdna_end": null,
          "cdna_length": 19940,
          "mane_select": "NM_001376.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 77,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg",
          "transcript": "ENST00000681574.1",
          "protein_id": "ENSP00000505523.1",
          "transcript_support_level": null,
          "aa_start": 3981,
          "aa_end": null,
          "aa_length": 4672,
          "cds_start": 11942,
          "cds_end": null,
          "cds_length": 14019,
          "cdna_start": 12061,
          "cdna_end": null,
          "cdna_length": 14519,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg",
          "transcript": "ENST00000679720.1",
          "protein_id": "ENSP00000505938.1",
          "transcript_support_level": null,
          "aa_start": 3981,
          "aa_end": null,
          "aa_length": 4637,
          "cds_start": 11942,
          "cds_end": null,
          "cds_length": 13914,
          "cdna_start": 12061,
          "cdna_end": null,
          "cdna_length": 19903,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg",
          "transcript": "ENST00000644881.2",
          "protein_id": "ENSP00000495022.2",
          "transcript_support_level": null,
          "aa_start": 3981,
          "aa_end": null,
          "aa_length": 4604,
          "cds_start": 11942,
          "cds_end": null,
          "cds_length": 13815,
          "cdna_start": 12061,
          "cdna_end": null,
          "cdna_length": 14291,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant",
            "splice_region_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 77,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "c.11795C>G",
          "hgvs_p": "p.Thr3932Arg",
          "transcript": "ENST00000645149.2",
          "protein_id": "ENSP00000495944.2",
          "transcript_support_level": null,
          "aa_start": 3932,
          "aa_end": null,
          "aa_length": 4597,
          "cds_start": 11795,
          "cds_end": null,
          "cds_length": 13794,
          "cdna_start": 11914,
          "cdna_end": null,
          "cdna_length": 14134,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.494C>G",
          "hgvs_p": null,
          "transcript": "ENST00000556139.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 818,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.1075C>G",
          "hgvs_p": null,
          "transcript": "ENST00000556499.3",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 1416,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.1896C>G",
          "hgvs_p": null,
          "transcript": "ENST00000643437.1",
          "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": 4773,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.1771C>G",
          "hgvs_p": null,
          "transcript": "ENST00000643829.1",
          "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": 4050,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.2061C>G",
          "hgvs_p": null,
          "transcript": "ENST00000644794.1",
          "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": 4842,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 76,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.11691C>G",
          "hgvs_p": null,
          "transcript": "ENST00000645039.2",
          "protein_id": "ENSP00000495220.2",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 14031,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.188C>G",
          "hgvs_p": null,
          "transcript": "ENST00000645085.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 2397,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.2605C>G",
          "hgvs_p": null,
          "transcript": "ENST00000645697.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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        },
        {
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          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.1183C>G",
          "hgvs_p": null,
          "transcript": "ENST00000647204.2",
          "protein_id": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4235,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 44,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.5496C>G",
          "hgvs_p": null,
          "transcript": "ENST00000647366.1",
          "protein_id": null,
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          "aa_start": null,
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          "cdna_length": 7322,
          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 71,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.11942C>G",
          "hgvs_p": null,
          "transcript": "ENST00000679486.1",
          "protein_id": "ENSP00000506688.1",
          "transcript_support_level": null,
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.11767C>G",
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          "transcript": "ENST00000679629.1",
          "protein_id": "ENSP00000505589.1",
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        },
        {
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          "strand": true,
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            "non_coding_transcript_exon_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.*3024C>G",
          "hgvs_p": null,
          "transcript": "ENST00000679910.1",
          "protein_id": "ENSP00000506521.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_length": 14277,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 78,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.11942C>G",
          "hgvs_p": null,
          "transcript": "ENST00000680120.1",
          "protein_id": "ENSP00000504863.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_length": 14261,
          "mane_select": null,
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          "gene_hgnc_id": null,
          "hgvs_c": "n.203-4805G>C",
          "hgvs_p": null,
          "transcript": "ENST00000762208.1",
          "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": 657,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.-201C>G",
          "hgvs_p": null,
          "transcript": "ENST00000644239.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2298,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DYNC1H1",
          "gene_hgnc_id": 2961,
          "hgvs_c": "n.-86C>G",
          "hgvs_p": null,
          "transcript": "ENST00000644888.1",
          "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": 968,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "DYNC1H1",
      "gene_hgnc_id": 2961,
      "dbsnp": "rs138428684",
      "frequency_reference_population": 0.003975684,
      "hom_count_reference_population": 18,
      "allele_count_reference_population": 6417,
      "gnomad_exomes_af": 0.00410678,
      "gnomad_genomes_af": 0.00271771,
      "gnomad_exomes_ac": 6003,
      "gnomad_genomes_ac": 414,
      "gnomad_exomes_homalt": 17,
      "gnomad_genomes_homalt": 1,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.009332239627838135,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.6460000276565552,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": 0.243,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.4002,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.15,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 6.108,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.958525045471103,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -20,
          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000360184.10",
          "gene_symbol": "DYNC1H1",
          "hgnc_id": 2961,
          "effects": [
            "missense_variant",
            "splice_region_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.11942C>G",
          "hgvs_p": "p.Thr3981Arg"
        },
        {
          "score": -16,
          "benign_score": 16,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000553701.1",
          "gene_symbol": "ENSG00000293472",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.347-4805G>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": " autosomal dominant 13,Autosomal dominant cerebellar ataxia,Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures,Charcot-Marie-Tooth disease,Charcot-Marie-Tooth disease axonal type 2O,DYNC1H1-related disorder,Inborn genetic diseases,Intellectual disability,not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:9 B:6",
      "phenotype_combined": "not specified|not provided|Charcot-Marie-Tooth disease axonal type 2O|Autosomal dominant cerebellar ataxia|Charcot-Marie-Tooth disease|Inborn genetic diseases|Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures;Charcot-Marie-Tooth disease axonal type 2O;Intellectual disability, autosomal dominant 13|DYNC1H1-related disorder",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}