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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-20155479-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=20155479&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 20155479,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_004586.3",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2142G>A",
          "hgvs_p": "p.Gln714Gln",
          "transcript": "NM_004586.3",
          "protein_id": "NP_004577.1",
          "transcript_support_level": null,
          "aa_start": 714,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": 2142,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000379565.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_004586.3"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2142G>A",
          "hgvs_p": "p.Gln714Gln",
          "transcript": "ENST00000379565.9",
          "protein_id": "ENSP00000368884.3",
          "transcript_support_level": 1,
          "aa_start": 714,
          "aa_end": null,
          "aa_length": 740,
          "cds_start": 2142,
          "cds_end": null,
          "cds_length": 2223,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_004586.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000379565.9"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2190G>A",
          "hgvs_p": "p.Gln730Gln",
          "transcript": "ENST00000952699.1",
          "protein_id": "ENSP00000622758.1",
          "transcript_support_level": null,
          "aa_start": 730,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 2190,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000952699.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2160G>A",
          "hgvs_p": "p.Gln720Gln",
          "transcript": "ENST00000916293.1",
          "protein_id": "ENSP00000586352.1",
          "transcript_support_level": null,
          "aa_start": 720,
          "aa_end": null,
          "aa_length": 746,
          "cds_start": 2160,
          "cds_end": null,
          "cds_length": 2241,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000916293.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2157G>A",
          "hgvs_p": "p.Gln719Gln",
          "transcript": "ENST00000952703.1",
          "protein_id": "ENSP00000622762.1",
          "transcript_support_level": null,
          "aa_start": 719,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2157,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000952703.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2148G>A",
          "hgvs_p": "p.Gln716Gln",
          "transcript": "ENST00000952700.1",
          "protein_id": "ENSP00000622759.1",
          "transcript_support_level": null,
          "aa_start": 716,
          "aa_end": null,
          "aa_length": 742,
          "cds_start": 2148,
          "cds_end": null,
          "cds_length": 2229,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000952700.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2136G>A",
          "hgvs_p": "p.Gln712Gln",
          "transcript": "ENST00000916295.1",
          "protein_id": "ENSP00000586354.1",
          "transcript_support_level": null,
          "aa_start": 712,
          "aa_end": null,
          "aa_length": 738,
          "cds_start": 2136,
          "cds_end": null,
          "cds_length": 2217,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000916295.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2133G>A",
          "hgvs_p": "p.Gln711Gln",
          "transcript": "ENST00000916291.1",
          "protein_id": "ENSP00000586350.1",
          "transcript_support_level": null,
          "aa_start": 711,
          "aa_end": null,
          "aa_length": 737,
          "cds_start": 2133,
          "cds_end": null,
          "cds_length": 2214,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000916291.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2103G>A",
          "hgvs_p": "p.Gln701Gln",
          "transcript": "ENST00000952702.1",
          "protein_id": "ENSP00000622761.1",
          "transcript_support_level": null,
          "aa_start": 701,
          "aa_end": null,
          "aa_length": 727,
          "cds_start": 2103,
          "cds_end": null,
          "cds_length": 2184,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000952702.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2085G>A",
          "hgvs_p": "p.Gln695Gln",
          "transcript": "ENST00000916294.1",
          "protein_id": "ENSP00000586353.1",
          "transcript_support_level": null,
          "aa_start": 695,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 2085,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000916294.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2061G>A",
          "hgvs_p": "p.Gln687Gln",
          "transcript": "ENST00000952698.1",
          "protein_id": "ENSP00000622757.1",
          "transcript_support_level": null,
          "aa_start": 687,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": 2061,
          "cds_end": null,
          "cds_length": 2142,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000952698.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "NM_001438340.1",
          "protein_id": "NP_001425269.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001438340.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000642835.1",
          "protein_id": "ENSP00000494769.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000642835.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000643085.1",
          "protein_id": "ENSP00000496271.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
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          "cds_length": 2139,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000643085.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000643337.1",
          "protein_id": "ENSP00000493487.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000643337.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000643402.1",
          "protein_id": "ENSP00000493862.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
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          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000643402.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000644368.1",
          "protein_id": "ENSP00000495776.1",
          "transcript_support_level": null,
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          "cds_start": 2058,
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          "biotype": "protein_coding",
          "feature": "ENST00000644368.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 25,
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          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000645270.1",
          "protein_id": "ENSP00000494967.1",
          "transcript_support_level": null,
          "aa_start": 686,
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          "aa_length": 712,
          "cds_start": 2058,
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          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000645270.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000646610.1",
          "protein_id": "ENSP00000495462.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 712,
          "cds_start": 2058,
          "cds_end": null,
          "cds_length": 2139,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000646610.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "c.2058G>A",
          "hgvs_p": "p.Gln686Gln",
          "transcript": "ENST00000647265.1",
          "protein_id": "ENSP00000494220.1",
          "transcript_support_level": null,
          "aa_start": 686,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*1514G>A",
          "hgvs_p": null,
          "transcript": "ENST00000643073.1",
          "protein_id": "ENSP00000495839.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000643073.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*1363G>A",
          "hgvs_p": null,
          "transcript": "ENST00000645268.1",
          "protein_id": "ENSP00000496226.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000645268.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*1514G>A",
          "hgvs_p": null,
          "transcript": "ENST00000643073.1",
          "protein_id": "ENSP00000495839.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000643073.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS6KA3",
          "gene_hgnc_id": 10432,
          "hgvs_c": "n.*1363G>A",
          "hgvs_p": null,
          "transcript": "ENST00000645268.1",
          "protein_id": "ENSP00000496226.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000645268.1"
        }
      ],
      "gene_symbol": "RPS6KA3",
      "gene_hgnc_id": 10432,
      "dbsnp": "rs1241566447",
      "frequency_reference_population": 0.000003308429,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 4,
      "gnomad_exomes_af": 0.00000273345,
      "gnomad_genomes_af": 0.00000896716,
      "gnomad_exomes_ac": 3,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.5600000023841858,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.019999999552965164,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.56,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.06,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.02,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_004586.3",
          "gene_symbol": "RPS6KA3",
          "hgnc_id": 10432,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,XL",
          "hgvs_c": "c.2142G>A",
          "hgvs_p": "p.Gln714Gln"
        }
      ],
      "clinvar_disease": " X-linked 19,Coffin-Lowry syndrome,Intellectual disability,RPS6KA3-related disorder",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "Coffin-Lowry syndrome;Intellectual disability, X-linked 19|RPS6KA3-related disorder",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}