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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: 3-52291925-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=52291925&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 52291925,
      "ref": "A",
      "alt": "G",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "ENST00000436784.7",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.705+3A>G",
          "hgvs_p": null,
          "transcript": "NM_145262.4",
          "protein_id": "NP_660305.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 523,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1572,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3791,
          "mane_select": "ENST00000436784.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.705+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000436784.7",
          "protein_id": "ENSP00000389175.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 523,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1572,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3791,
          "mane_select": "NM_145262.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.530-335A>G",
          "hgvs_p": null,
          "transcript": "ENST00000477382.1",
          "protein_id": "ENSP00000419008.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 234,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 705,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1304,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.529+814A>G",
          "hgvs_p": null,
          "transcript": "ENST00000473032.5",
          "protein_id": "ENSP00000418951.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 205,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 618,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 935,
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.799-335A>G",
          "hgvs_p": null,
          "transcript": "ENST00000473583.1",
          "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": 1021,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.*68+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000486393.5",
          "protein_id": "ENSP00000419868.1",
          "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": 2019,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.705+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001437621.1",
          "protein_id": "NP_001424550.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 523,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1572,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3980,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.453+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000461183.5",
          "protein_id": "ENSP00000417264.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 283,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 852,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 889,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.324+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000471180.5",
          "protein_id": "ENSP00000417526.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 240,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 723,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 992,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.530-335A>G",
          "hgvs_p": null,
          "transcript": "NM_001144951.2",
          "protein_id": "NP_001138423.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 234,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 705,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3615,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.530-335A>G",
          "hgvs_p": null,
          "transcript": "NM_001437622.1",
          "protein_id": "NP_001424551.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 234,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 705,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3804,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.530-335A>G",
          "hgvs_p": null,
          "transcript": "ENST00000305690.12",
          "protein_id": "ENSP00000301965.9",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 234,
          "cds_start": -4,
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          "cds_length": 705,
          "cdna_start": null,
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          "cdna_length": 1371,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.999+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000489173.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2083,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK-AS1",
          "gene_hgnc_id": 41043,
          "hgvs_c": "n.500+1102T>C",
          "hgvs_p": null,
          "transcript": "ENST00000493616.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
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          "cdna_start": null,
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          "cdna_length": 645,
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK-AS1",
          "gene_hgnc_id": 41043,
          "hgvs_c": "n.205+1102T>C",
          "hgvs_p": null,
          "transcript": "ENST00000741311.1",
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          "cdna_start": null,
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          "cdna_length": 543,
          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK-AS1",
          "gene_hgnc_id": 41043,
          "hgvs_c": "n.91-2990T>C",
          "hgvs_p": null,
          "transcript": "ENST00000741312.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 446,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.795+3A>G",
          "hgvs_p": null,
          "transcript": "NR_026699.2",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 3793,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.377+3A>G",
          "hgvs_p": null,
          "transcript": "NR_026700.2",
          "protein_id": null,
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          "cdna_length": 2785,
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        },
        {
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          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.793+3A>G",
          "hgvs_p": null,
          "transcript": "NR_026701.2",
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          "cdna_length": 3677,
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          "biotype": null,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
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          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.617+814A>G",
          "hgvs_p": null,
          "transcript": "NR_026702.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2715,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "n.1428+3A>G",
          "hgvs_p": null,
          "transcript": "NR_199363.1",
          "protein_id": null,
          "transcript_support_level": null,
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        {
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          "protein_coding": false,
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        {
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          "exon_rank": null,
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          "transcript": "XM_017005730.2",
          "protein_id": "XP_016861219.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "protein_coding": true,
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          "exon_count": 5,
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          "gene_symbol": "GLYCTK",
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          "transcript": "XM_047447465.1",
          "protein_id": "XP_047303421.1",
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          "cdna_start": null,
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        },
        {
          "aa_ref": null,
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          "protein_coding": true,
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          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 6,
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          "gene_symbol": "GLYCTK",
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          "hgvs_c": "c.705+3A>G",
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          "transcript": "XM_047447466.1",
          "protein_id": "XP_047303422.1",
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        },
        {
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          "protein_coding": true,
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            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "gene_symbol": "GLYCTK",
          "gene_hgnc_id": 24247,
          "hgvs_c": "c.324+3A>G",
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          "transcript": "XM_047447467.1",
          "protein_id": "XP_047303423.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1113,
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        }
      ],
      "gene_symbol": "GLYCTK",
      "gene_hgnc_id": 24247,
      "dbsnp": "rs199697098",
      "frequency_reference_population": 0.000012416082,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 20,
      "gnomad_exomes_af": 0.0000102833,
      "gnomad_genomes_af": 0.000032864,
      "gnomad_exomes_ac": 15,
      "gnomad_genomes_ac": 5,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8600000143051147,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.42399999499320984,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.86,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.042,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.31,
      "spliceai_max_prediction": "Uncertain_significance",
      "dbscsnv_ada_score": 0.0361523270581425,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000436784.7",
          "gene_symbol": "GLYCTK",
          "hgnc_id": 24247,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.705+3A>G",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000493616.2",
          "gene_symbol": "GLYCTK-AS1",
          "hgnc_id": 41043,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.500+1102T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}