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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: 18-51065563-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=51065563&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "18",
      "pos": 51065563,
      "ref": "C",
      "alt": "T",
      "effect": "stop_gained",
      "transcript": "ENST00000342988.8",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "NM_005359.6",
          "protein_id": "NP_005350.1",
          "transcript_support_level": null,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1634,
          "cdna_end": null,
          "cdna_length": 8772,
          "mane_select": "ENST00000342988.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000342988.8",
          "protein_id": "ENSP00000341551.3",
          "transcript_support_level": 5,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1634,
          "cdna_end": null,
          "cdna_length": 8772,
          "mane_select": "NM_005359.6",
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "n.3097C>T",
          "hgvs_p": null,
          "transcript": "ENST00000591126.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": 4970,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1177C>T",
          "hgvs_p": "p.Gln393*",
          "transcript": "ENST00000714264.1",
          "protein_id": "ENSP00000519545.1",
          "transcript_support_level": null,
          "aa_start": 393,
          "aa_end": null,
          "aa_length": 579,
          "cds_start": 1177,
          "cds_end": null,
          "cds_length": 1740,
          "cdna_start": 1715,
          "cdna_end": null,
          "cdna_length": 3592,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1174C>T",
          "hgvs_p": "p.Gln392*",
          "transcript": "ENST00000714270.1",
          "protein_id": "ENSP00000519551.1",
          "transcript_support_level": null,
          "aa_start": 392,
          "aa_end": null,
          "aa_length": 578,
          "cds_start": 1174,
          "cds_end": null,
          "cds_length": 1737,
          "cdna_start": 1702,
          "cdna_end": null,
          "cdna_length": 3573,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1135C>T",
          "hgvs_p": "p.Gln379*",
          "transcript": "ENST00000714261.1",
          "protein_id": "ENSP00000519542.1",
          "transcript_support_level": null,
          "aa_start": 379,
          "aa_end": null,
          "aa_length": 565,
          "cds_start": 1135,
          "cds_end": null,
          "cds_length": 1698,
          "cdna_start": 1676,
          "cdna_end": null,
          "cdna_length": 3855,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "NM_001407041.1",
          "protein_id": "NP_001393970.1",
          "transcript_support_level": null,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1219,
          "cdna_end": null,
          "cdna_length": 8357,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "NM_001407042.1",
          "protein_id": "NP_001393971.1",
          "transcript_support_level": null,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1287,
          "cdna_end": null,
          "cdna_length": 8425,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000398417.6",
          "protein_id": "ENSP00000381452.1",
          "transcript_support_level": 5,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1354,
          "cdna_end": null,
          "cdna_length": 8495,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000588860.6",
          "protein_id": "ENSP00000465878.2",
          "transcript_support_level": 4,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": 1361,
          "cdna_end": null,
          "cdna_length": 8474,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000589076.6",
          "protein_id": "ENSP00000466934.2",
          "transcript_support_level": 5,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1096,
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          "cdna_start": 1400,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000589941.2",
          "protein_id": "ENSP00000465874.2",
          "transcript_support_level": 3,
          "aa_start": 366,
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          "aa_length": 552,
          "cds_start": 1096,
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          "cdna_start": 1803,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000590061.2",
          "protein_id": "ENSP00000464772.2",
          "transcript_support_level": 4,
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          "cds_start": 1096,
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          "cdna_start": 1219,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1072C>T",
          "hgvs_p": "p.Gln358*",
          "transcript": "ENST00000714272.1",
          "protein_id": "ENSP00000519553.1",
          "transcript_support_level": null,
          "aa_start": 358,
          "aa_end": null,
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          "cds_start": 1072,
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          "cdna_start": 1599,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1066C>T",
          "hgvs_p": "p.Gln356*",
          "transcript": "ENST00000714268.1",
          "protein_id": "ENSP00000519549.1",
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          "cds_start": 1066,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "ENST00000593223.2",
          "protein_id": "ENSP00000466118.2",
          "transcript_support_level": 3,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 493,
          "cds_start": 1096,
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          "cdna_start": 1628,
          "cdna_end": null,
          "cdna_length": 4980,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.883C>T",
          "hgvs_p": "p.Gln295*",
          "transcript": "ENST00000714266.1",
          "protein_id": "ENSP00000519547.1",
          "transcript_support_level": null,
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        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
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          "exon_rank_end": null,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.808C>T",
          "hgvs_p": "p.Gln270*",
          "transcript": "ENST00000588745.5",
          "protein_id": "ENSP00000464901.1",
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          "cdna_start": 808,
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*",
          "transcript": "NM_001407043.1",
          "protein_id": "NP_001393972.1",
          "transcript_support_level": null,
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          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "n.1096C>T",
          "hgvs_p": null,
          "transcript": "ENST00000611848.2",
          "protein_id": "ENSP00000478613.2",
          "transcript_support_level": 5,
          "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": 2906,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
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          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "n.955+5647C>T",
          "hgvs_p": null,
          "transcript": "ENST00000592186.5",
          "protein_id": "ENSP00000468611.1",
          "transcript_support_level": 5,
          "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": 1306,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "SMAD4",
          "gene_hgnc_id": 6770,
          "hgvs_c": "n.1002+94C>T",
          "hgvs_p": null,
          "transcript": "ENST00000714265.1",
          "protein_id": "ENSP00000519546.1",
          "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": 8635,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SMAD4",
      "gene_hgnc_id": 6770,
      "dbsnp": "rs1060500733",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.6600000262260437,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.17000000178813934,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.66,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 7.758,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0.17,
      "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": 18,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Very_Strong",
      "acmg_by_gene": [
        {
          "score": 18,
          "benign_score": 0,
          "pathogenic_score": 18,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000342988.8",
          "gene_symbol": "SMAD4",
          "hgnc_id": 6770,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1096C>T",
          "hgvs_p": "p.Gln366*"
        }
      ],
      "clinvar_disease": "Familial thoracic aortic aneurysm and aortic dissection,Hereditary cancer-predisposing syndrome,Juvenile polyposis syndrome",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:2",
      "phenotype_combined": "Juvenile polyposis syndrome|Familial thoracic aortic aneurysm and aortic dissection;Hereditary cancer-predisposing syndrome",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}