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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: 4-168898684-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=168898684&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 168898684,
      "ref": "A",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000505667.6",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.2442A>C",
          "hgvs_p": "p.Thr814Thr",
          "transcript": "NM_001166108.2",
          "protein_id": "NP_001159580.1",
          "transcript_support_level": null,
          "aa_start": 814,
          "aa_end": null,
          "aa_length": 1123,
          "cds_start": 2442,
          "cds_end": null,
          "cds_length": 3372,
          "cdna_start": 2667,
          "cdna_end": null,
          "cdna_length": 5858,
          "mane_select": "ENST00000505667.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.2442A>C",
          "hgvs_p": "p.Thr814Thr",
          "transcript": "ENST00000505667.6",
          "protein_id": "ENSP00000425556.1",
          "transcript_support_level": 1,
          "aa_start": 814,
          "aa_end": null,
          "aa_length": 1123,
          "cds_start": 2442,
          "cds_end": null,
          "cds_length": 3372,
          "cdna_start": 2667,
          "cdna_end": null,
          "cdna_length": 5858,
          "mane_select": "NM_001166108.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.2391A>C",
          "hgvs_p": "p.Thr797Thr",
          "transcript": "ENST00000261509.10",
          "protein_id": "ENSP00000261509.6",
          "transcript_support_level": 1,
          "aa_start": 797,
          "aa_end": null,
          "aa_length": 1106,
          "cds_start": 2391,
          "cds_end": null,
          "cds_length": 3321,
          "cdna_start": 2602,
          "cdna_end": null,
          "cdna_length": 5809,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.930A>C",
          "hgvs_p": "p.Thr310Thr",
          "transcript": "ENST00000507735.6",
          "protein_id": "ENSP00000424016.1",
          "transcript_support_level": 1,
          "aa_start": 310,
          "aa_end": null,
          "aa_length": 672,
          "cds_start": 930,
          "cds_end": null,
          "cds_length": 2019,
          "cdna_start": 1243,
          "cdna_end": null,
          "cdna_length": 4392,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "n.708A>C",
          "hgvs_p": null,
          "transcript": "ENST00000507699.1",
          "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": 3829,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.2391A>C",
          "hgvs_p": "p.Thr797Thr",
          "transcript": "NM_016081.4",
          "protein_id": "NP_057165.3",
          "transcript_support_level": null,
          "aa_start": 797,
          "aa_end": null,
          "aa_length": 1106,
          "cds_start": 2391,
          "cds_end": null,
          "cds_length": 3321,
          "cdna_start": 2616,
          "cdna_end": null,
          "cdna_length": 5807,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.1245A>C",
          "hgvs_p": "p.Thr415Thr",
          "transcript": "NM_001166109.2",
          "protein_id": "NP_001159581.1",
          "transcript_support_level": null,
          "aa_start": 415,
          "aa_end": null,
          "aa_length": 777,
          "cds_start": 1245,
          "cds_end": null,
          "cds_length": 2334,
          "cdna_start": 1806,
          "cdna_end": null,
          "cdna_length": 4951,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.1245A>C",
          "hgvs_p": "p.Thr415Thr",
          "transcript": "ENST00000512127.5",
          "protein_id": "ENSP00000426947.1",
          "transcript_support_level": 2,
          "aa_start": 415,
          "aa_end": null,
          "aa_length": 777,
          "cds_start": 1245,
          "cds_end": null,
          "cds_length": 2334,
          "cdna_start": 1767,
          "cdna_end": null,
          "cdna_length": 2958,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.930A>C",
          "hgvs_p": "p.Thr310Thr",
          "transcript": "NM_001166110.2",
          "protein_id": "NP_001159582.1",
          "transcript_support_level": null,
          "aa_start": 310,
          "aa_end": null,
          "aa_length": 672,
          "cds_start": 930,
          "cds_end": null,
          "cds_length": 2019,
          "cdna_start": 1176,
          "cdna_end": null,
          "cdna_length": 4321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.321A>C",
          "hgvs_p": "p.Thr107Thr",
          "transcript": "NM_001367568.1",
          "protein_id": "NP_001354497.1",
          "transcript_support_level": null,
          "aa_start": 107,
          "aa_end": null,
          "aa_length": 469,
          "cds_start": 321,
          "cds_end": null,
          "cds_length": 1410,
          "cdna_start": 555,
          "cdna_end": null,
          "cdna_length": 3700,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.321A>C",
          "hgvs_p": "p.Thr107Thr",
          "transcript": "ENST00000704822.1",
          "protein_id": "ENSP00000516055.1",
          "transcript_support_level": null,
          "aa_start": 107,
          "aa_end": null,
          "aa_length": 469,
          "cds_start": 321,
          "cds_end": null,
          "cds_length": 1410,
          "cdna_start": 606,
          "cdna_end": null,
          "cdna_length": 3736,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.270A>C",
          "hgvs_p": "p.Thr90Thr",
          "transcript": "NM_001367569.1",
          "protein_id": "NP_001354498.1",
          "transcript_support_level": null,
          "aa_start": 90,
          "aa_end": null,
          "aa_length": 452,
          "cds_start": 270,
          "cds_end": null,
          "cds_length": 1359,
          "cdna_start": 504,
          "cdna_end": null,
          "cdna_length": 3649,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.321A>C",
          "hgvs_p": "p.Thr107Thr",
          "transcript": "NM_001367570.1",
          "protein_id": "NP_001354499.1",
          "transcript_support_level": null,
          "aa_start": 107,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 321,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 555,
          "cdna_end": null,
          "cdna_length": 3746,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.270A>C",
          "hgvs_p": "p.Thr90Thr",
          "transcript": "NM_001367567.1",
          "protein_id": "NP_001354496.1",
          "transcript_support_level": null,
          "aa_start": 90,
          "aa_end": null,
          "aa_length": 399,
          "cds_start": 270,
          "cds_end": null,
          "cds_length": 1200,
          "cdna_start": 504,
          "cdna_end": null,
          "cdna_length": 3695,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
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          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.270A>C",
          "hgvs_p": "p.Thr90Thr",
          "transcript": "ENST00000393726.7",
          "protein_id": "ENSP00000377327.3",
          "transcript_support_level": 3,
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          "aa_end": null,
          "aa_length": 163,
          "cds_start": 270,
          "cds_end": null,
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          "cdna_start": 594,
          "cdna_end": null,
          "cdna_length": 817,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.270A>C",
          "hgvs_p": "p.Thr90Thr",
          "transcript": "ENST00000510998.5",
          "protein_id": "ENSP00000422135.1",
          "transcript_support_level": 4,
          "aa_start": 90,
          "aa_end": null,
          "aa_length": 89,
          "cds_start": 270,
          "cds_end": null,
          "cds_length": 272,
          "cdna_start": 543,
          "cdna_end": null,
          "cdna_length": 545,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.3318A>C",
          "hgvs_p": "p.Thr1106Thr",
          "transcript": "XM_011531768.3",
          "protein_id": "XP_011530070.1",
          "transcript_support_level": null,
          "aa_start": 1106,
          "aa_end": null,
          "aa_length": 1468,
          "cds_start": 3318,
          "cds_end": null,
          "cds_length": 4407,
          "cdna_start": 3678,
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          "cdna_length": 6823,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.3267A>C",
          "hgvs_p": "p.Thr1089Thr",
          "transcript": "XM_011531769.3",
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          "aa_end": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.3318A>C",
          "hgvs_p": "p.Thr1106Thr",
          "transcript": "XM_047449861.1",
          "protein_id": "XP_047305817.1",
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          "cds_start": 3318,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "c.3267A>C",
          "hgvs_p": "p.Thr1089Thr",
          "transcript": "XM_047449862.1",
          "protein_id": "XP_047305818.1",
          "transcript_support_level": null,
          "aa_start": 1089,
          "aa_end": null,
          "aa_length": 1398,
          "cds_start": 3267,
          "cds_end": null,
          "cds_length": 4197,
          "cdna_start": 3627,
          "cdna_end": null,
          "cdna_length": 4595,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CBR4",
          "gene_hgnc_id": 25891,
          "hgvs_c": "n.873-2932T>G",
          "hgvs_p": null,
          "transcript": "XR_001741341.2",
          "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": 1178,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "CBR4",
          "gene_hgnc_id": 25891,
          "hgvs_c": "n.873-3919T>G",
          "hgvs_p": null,
          "transcript": "XR_007057980.1",
          "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": 1018,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PALLD",
          "gene_hgnc_id": 17068,
          "hgvs_c": "n.*168A>C",
          "hgvs_p": null,
          "transcript": "ENST00000511611.1",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": 533,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PALLD",
      "gene_hgnc_id": 17068,
      "dbsnp": "rs113676921",
      "frequency_reference_population": 0.000006569698,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.0000065697,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8500000238418579,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.85,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.356,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -10,
      "acmg_classification": "Benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Very_Strong",
      "acmg_by_gene": [
        {
          "score": -10,
          "benign_score": 12,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000505667.6",
          "gene_symbol": "PALLD",
          "hgnc_id": 17068,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2442A>C",
          "hgvs_p": "p.Thr814Thr"
        },
        {
          "score": -10,
          "benign_score": 12,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000510042.5",
          "gene_symbol": "CBR4",
          "hgnc_id": 25891,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "n.*259-3919T>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Pancreatic adenocarcinoma,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "Pancreatic adenocarcinoma|not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}