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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: 12-63617303-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=63617303&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 63617303,
      "ref": "C",
      "alt": "T",
      "effect": "splice_donor_variant,intron_variant",
      "transcript": "NM_173812.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "NM_173812.5",
          "protein_id": "NP_776173.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 758,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2277,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000324472.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_173812.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000324472.9",
          "protein_id": "ENSP00000315988.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 758,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2277,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_173812.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000324472.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "n.*609+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000306389.7",
          "protein_id": "ENSP00000445878.1",
          "transcript_support_level": 1,
          "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": "nonsense_mediated_decay",
          "feature": "ENST00000306389.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000882292.1",
          "protein_id": "ENSP00000552351.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 738,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2217,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882292.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961037.1",
          "protein_id": "ENSP00000631096.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 734,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2205,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961037.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000882290.1",
          "protein_id": "ENSP00000552349.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 716,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2151,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882290.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961030.1",
          "protein_id": "ENSP00000631089.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 714,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2145,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961030.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000882291.1",
          "protein_id": "ENSP00000552350.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 696,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2091,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882291.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961035.1",
          "protein_id": "ENSP00000631094.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 692,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2079,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961035.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000882293.1",
          "protein_id": "ENSP00000552352.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 690,
          "cds_start": null,
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          "cds_length": 2073,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882293.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1068+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961032.1",
          "protein_id": "ENSP00000631091.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 684,
          "cds_start": null,
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          "cds_length": 2055,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961031.1",
          "protein_id": "ENSP00000631090.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 17,
          "intron_rank": 9,
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          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1068+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961033.1",
          "protein_id": "ENSP00000631092.1",
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          "aa_end": null,
          "aa_length": 664,
          "cds_start": null,
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          "cds_length": 1995,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000961033.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.589-34778G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961036.1",
          "protein_id": "ENSP00000631095.1",
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        {
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          "canonical": false,
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          "exon_count": 8,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.589-34778G>A",
          "hgvs_p": null,
          "transcript": "ENST00000961034.1",
          "protein_id": "ENSP00000631093.1",
          "transcript_support_level": null,
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          "aa_length": 377,
          "cds_start": null,
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          "cds_length": 1134,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000961034.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.216+1G>A",
          "hgvs_p": null,
          "transcript": "ENST00000541083.1",
          "protein_id": "ENSP00000443126.1",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 123,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000541083.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 21,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
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          "transcript": "XM_024448944.2",
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        {
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 22,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "XM_047428721.1",
          "protein_id": "XP_047284677.1",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 21,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "XM_024448945.2",
          "protein_id": "XP_024304713.1",
          "transcript_support_level": null,
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          "aa_length": 716,
          "cds_start": null,
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          "cds_length": 2151,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_024448945.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1068+1G>A",
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          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "DPY19L2",
          "gene_hgnc_id": 19414,
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null,
          "transcript": "XM_024448957.2",
          "protein_id": "XP_024304725.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 408,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1227,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_024448957.2"
        }
      ],
      "gene_symbol": "DPY19L2",
      "gene_hgnc_id": 19414,
      "dbsnp": "rs868256749",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": 0,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 0,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.11999999731779099,
      "computational_prediction_selected": "Uncertain_significance",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.9380000233650208,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.12,
      "bayesdelnoaf_prediction": "Uncertain_significance",
      "phylop100way_score": 5.195,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.78,
      "spliceai_max_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.999972537349306,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 5,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate,PM2,PP5",
      "acmg_by_gene": [
        {
          "score": 5,
          "benign_score": 0,
          "pathogenic_score": 5,
          "criteria": [
            "PVS1_Moderate",
            "PM2",
            "PP5"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_173812.5",
          "gene_symbol": "DPY19L2",
          "hgnc_id": 19414,
          "effects": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1218+1G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Spermatogenic failure 9",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Spermatogenic failure 9",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}