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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: X-154420926-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=154420926&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 154420926,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000601016.6",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.801G>A",
          "hgvs_p": "p.Thr267Thr",
          "transcript": "NM_000116.5",
          "protein_id": "NP_000107.1",
          "transcript_support_level": null,
          "aa_start": 267,
          "aa_end": null,
          "aa_length": 292,
          "cds_start": 801,
          "cds_end": null,
          "cds_length": 879,
          "cdna_start": 1106,
          "cdna_end": null,
          "cdna_length": 1906,
          "mane_select": "ENST00000601016.6",
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.801G>A",
          "hgvs_p": "p.Thr267Thr",
          "transcript": "ENST00000601016.6",
          "protein_id": "ENSP00000469981.1",
          "transcript_support_level": 1,
          "aa_start": 267,
          "aa_end": null,
          "aa_length": 292,
          "cds_start": 801,
          "cds_end": null,
          "cds_length": 879,
          "cdna_start": 1106,
          "cdna_end": null,
          "cdna_length": 1906,
          "mane_select": "NM_000116.5",
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.765G>A",
          "hgvs_p": "p.Thr255Thr",
          "transcript": "ENST00000475699.6",
          "protein_id": "ENSP00000419854.3",
          "transcript_support_level": 1,
          "aa_start": 255,
          "aa_end": null,
          "aa_length": 280,
          "cds_start": 765,
          "cds_end": null,
          "cds_length": 843,
          "cdna_start": 1056,
          "cdna_end": null,
          "cdna_length": 1632,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.711G>A",
          "hgvs_p": "p.Thr237Thr",
          "transcript": "ENST00000369776.8",
          "protein_id": "ENSP00000358791.4",
          "transcript_support_level": 1,
          "aa_start": 237,
          "aa_end": null,
          "aa_length": 262,
          "cds_start": 711,
          "cds_end": null,
          "cds_length": 789,
          "cdna_start": 796,
          "cdna_end": null,
          "cdna_length": 1596,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.711G>A",
          "hgvs_p": "p.Thr237Thr",
          "transcript": "ENST00000612460.5",
          "protein_id": "ENSP00000481037.1",
          "transcript_support_level": 1,
          "aa_start": 237,
          "aa_end": null,
          "aa_length": 262,
          "cds_start": 711,
          "cds_end": null,
          "cds_length": 789,
          "cdna_start": 1016,
          "cdna_end": null,
          "cdna_length": 1790,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.669G>A",
          "hgvs_p": "p.Thr223Thr",
          "transcript": "ENST00000613002.4",
          "protein_id": "ENSP00000478154.1",
          "transcript_support_level": 1,
          "aa_start": 223,
          "aa_end": null,
          "aa_length": 248,
          "cds_start": 669,
          "cds_end": null,
          "cds_length": 747,
          "cdna_start": 972,
          "cdna_end": null,
          "cdna_length": 1485,
          "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": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "n.683G>A",
          "hgvs_p": null,
          "transcript": "ENST00000483674.3",
          "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": 1483,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.855G>A",
          "hgvs_p": "p.Thr285Thr",
          "transcript": "NM_001440856.1",
          "protein_id": "NP_001427785.1",
          "transcript_support_level": null,
          "aa_start": 285,
          "aa_end": null,
          "aa_length": 310,
          "cds_start": 855,
          "cds_end": null,
          "cds_length": 933,
          "cdna_start": 1160,
          "cdna_end": null,
          "cdna_length": 1960,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.813G>A",
          "hgvs_p": "p.Thr271Thr",
          "transcript": "NM_001303465.2",
          "protein_id": "NP_001290394.1",
          "transcript_support_level": null,
          "aa_start": 271,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": 813,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": 1118,
          "cdna_end": null,
          "cdna_length": 1918,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.813G>A",
          "hgvs_p": "p.Thr271Thr",
          "transcript": "ENST00000616020.5",
          "protein_id": "ENSP00000483636.2",
          "transcript_support_level": 5,
          "aa_start": 271,
          "aa_end": null,
          "aa_length": 296,
          "cds_start": 813,
          "cds_end": null,
          "cds_length": 891,
          "cdna_start": 813,
          "cdna_end": null,
          "cdna_length": 891,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.765G>A",
          "hgvs_p": "p.Thr255Thr",
          "transcript": "NM_001410698.1",
          "protein_id": "NP_001397627.1",
          "transcript_support_level": null,
          "aa_start": 255,
          "aa_end": null,
          "aa_length": 280,
          "cds_start": 765,
          "cds_end": null,
          "cds_length": 843,
          "cdna_start": 1070,
          "cdna_end": null,
          "cdna_length": 1870,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.759G>A",
          "hgvs_p": "p.Thr253Thr",
          "transcript": "NM_181312.4",
          "protein_id": "NP_851829.1",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 278,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 837,
          "cdna_start": 1064,
          "cdna_end": null,
          "cdna_length": 1864,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.759G>A",
          "hgvs_p": "p.Thr253Thr",
          "transcript": "ENST00000612012.5",
          "protein_id": "ENSP00000482070.2",
          "transcript_support_level": 5,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 278,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 837,
          "cdna_start": 953,
          "cdna_end": null,
          "cdna_length": 1230,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.723G>A",
          "hgvs_p": "p.Thr241Thr",
          "transcript": "NM_001440857.1",
          "protein_id": "NP_001427786.1",
          "transcript_support_level": null,
          "aa_start": 241,
          "aa_end": null,
          "aa_length": 266,
          "cds_start": 723,
          "cds_end": null,
          "cds_length": 801,
          "cdna_start": 1028,
          "cdna_end": null,
          "cdna_length": 1828,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.720G>A",
          "hgvs_p": "p.Thr240Thr",
          "transcript": "ENST00000652390.1",
          "protein_id": "ENSP00000498858.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 265,
          "cds_start": 720,
          "cds_end": null,
          "cds_length": 798,
          "cdna_start": 720,
          "cdna_end": null,
          "cdna_length": 1102,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.711G>A",
          "hgvs_p": "p.Thr237Thr",
          "transcript": "NM_181311.4",
          "protein_id": "NP_851828.1",
          "transcript_support_level": null,
          "aa_start": 237,
          "aa_end": null,
          "aa_length": 262,
          "cds_start": 711,
          "cds_end": null,
          "cds_length": 789,
          "cdna_start": 1016,
          "cdna_end": null,
          "cdna_length": 1816,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.669G>A",
          "hgvs_p": "p.Thr223Thr",
          "transcript": "NM_181313.4",
          "protein_id": "NP_851830.1",
          "transcript_support_level": null,
          "aa_start": 223,
          "aa_end": null,
          "aa_length": 248,
          "cds_start": 669,
          "cds_end": null,
          "cds_length": 747,
          "cdna_start": 974,
          "cdna_end": null,
          "cdna_length": 1774,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.594G>A",
          "hgvs_p": "p.Thr198Thr",
          "transcript": "ENST00000652358.1",
          "protein_id": "ENSP00000498464.1",
          "transcript_support_level": null,
          "aa_start": 198,
          "aa_end": null,
          "aa_length": 223,
          "cds_start": 594,
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          "cds_length": 672,
          "cdna_start": 705,
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          "cdna_length": 832,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.588G>A",
          "hgvs_p": "p.Thr196Thr",
          "transcript": "NM_001440858.1",
          "protein_id": "NP_001427787.1",
          "transcript_support_level": null,
          "aa_start": 196,
          "aa_end": null,
          "aa_length": 221,
          "cds_start": 588,
          "cds_end": null,
          "cds_length": 666,
          "cdna_start": 893,
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          "cdna_length": 1693,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "c.483G>A",
          "hgvs_p": "p.Thr161Thr",
          "transcript": "ENST00000652354.1",
          "protein_id": "ENSP00000498734.1",
          "transcript_support_level": null,
          "aa_start": 161,
          "aa_end": null,
          "aa_length": 186,
          "cds_start": 483,
          "cds_end": null,
          "cds_length": 561,
          "cdna_start": 669,
          "cdna_end": null,
          "cdna_length": 1469,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
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          "hgvs_c": "n.1428G>A",
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          "hgvs_c": "n.1122G>A",
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        },
        {
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          "exon_rank": 10,
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          "exon_count": 10,
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          "gene_symbol": "TAFAZZIN",
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          "hgvs_c": "n.*529G>A",
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          "transcript": "ENST00000615986.4",
          "protein_id": "ENSP00000480133.1",
          "transcript_support_level": 2,
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        },
        {
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          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 9,
          "intron_rank": null,
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          "gene_symbol": "TAFAZZIN",
          "gene_hgnc_id": 11577,
          "hgvs_c": "n.*814G>A",
          "hgvs_p": null,
          "transcript": "ENST00000617701.5",
          "protein_id": "ENSP00000481645.1",
          "transcript_support_level": 3,
          "aa_start": null,
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          "cds_length": null,
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          "cdna_length": 2158,
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          "feature": null
        }
      ],
      "gene_symbol": "TAFAZZIN",
      "gene_hgnc_id": 11577,
      "dbsnp": "rs781792950",
      "frequency_reference_population": 0.000043000084,
      "hom_count_reference_population": 17,
      "allele_count_reference_population": 52,
      "gnomad_exomes_af": 0.0000455385,
      "gnomad_genomes_af": 0.0000179651,
      "gnomad_exomes_ac": 50,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9599999785423279,
      "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": -0.96,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -10.556,
      "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": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000601016.6",
          "gene_symbol": "TAFAZZIN",
          "hgnc_id": 11577,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.801G>A",
          "hgvs_p": "p.Thr267Thr"
        }
      ],
      "clinvar_disease": "3-Methylglutaconic aciduria type 2,Cardiovascular phenotype",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "3-Methylglutaconic aciduria type 2|Cardiovascular phenotype",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}