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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: 15-42410651-G-GCAGT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=42410651&ref=G&alt=GCAGT&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 42410651,
      "ref": "G",
      "alt": "GCAGT",
      "effect": "frameshift_variant",
      "transcript": "NM_000070.3",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.2251_2254dupGTCA",
          "hgvs_p": "p.Asn752fs",
          "transcript": "NM_000070.3",
          "protein_id": "NP_000061.1",
          "transcript_support_level": null,
          "aa_start": 752,
          "aa_end": null,
          "aa_length": 821,
          "cds_start": 2255,
          "cds_end": null,
          "cds_length": 2466,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000397163.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000070.3"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.2251_2254dupGTCA",
          "hgvs_p": "p.Asn752fs",
          "transcript": "ENST00000397163.8",
          "protein_id": "ENSP00000380349.3",
          "transcript_support_level": 1,
          "aa_start": 752,
          "aa_end": null,
          "aa_length": 821,
          "cds_start": 2255,
          "cds_end": null,
          "cds_length": 2466,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000070.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000397163.8"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.2233_2236dupGTCA",
          "hgvs_p": "p.Asn746fs",
          "transcript": "ENST00000357568.8",
          "protein_id": "ENSP00000350181.3",
          "transcript_support_level": 1,
          "aa_start": 746,
          "aa_end": null,
          "aa_length": 815,
          "cds_start": 2237,
          "cds_end": null,
          "cds_length": 2448,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000357568.8"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.1975_1978dupGTCA",
          "hgvs_p": "p.Asn660fs",
          "transcript": "ENST00000349748.8",
          "protein_id": "ENSP00000183936.4",
          "transcript_support_level": 1,
          "aa_start": 660,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1979,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000349748.8"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.715_718dupGTCA",
          "hgvs_p": "p.Asn240fs",
          "transcript": "ENST00000397200.8",
          "protein_id": "ENSP00000380384.4",
          "transcript_support_level": 1,
          "aa_start": 240,
          "aa_end": null,
          "aa_length": 309,
          "cds_start": 719,
          "cds_end": null,
          "cds_length": 930,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000397200.8"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000561817.5",
          "protein_id": "ENSP00000456575.1",
          "transcript_support_level": 1,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 191,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 576,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000561817.5"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000337571.9",
          "protein_id": "ENSP00000336840.4",
          "transcript_support_level": 1,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000337571.9"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000397204.9",
          "protein_id": "ENSP00000380387.4",
          "transcript_support_level": 1,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000397204.9"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000673886.1",
          "protein_id": "ENSP00000501155.1",
          "transcript_support_level": null,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000673886.1"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000673928.1",
          "protein_id": "ENSP00000501099.1",
          "transcript_support_level": null,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000673928.1"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000674146.1",
          "protein_id": "ENSP00000501175.1",
          "transcript_support_level": null,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000674146.1"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.256_259dupGTCA",
          "hgvs_p": "p.Asn87fs",
          "transcript": "ENST00000674149.1",
          "protein_id": "ENSP00000501112.1",
          "transcript_support_level": null,
          "aa_start": 87,
          "aa_end": null,
          "aa_length": 156,
          "cds_start": 260,
          "cds_end": null,
          "cds_length": 471,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000674149.1"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.154_157dupGTCA",
          "hgvs_p": "p.Asn53fs",
          "transcript": "ENST00000673743.1",
          "protein_id": "ENSP00000500989.1",
          "transcript_support_level": null,
          "aa_start": 53,
          "aa_end": null,
          "aa_length": 122,
          "cds_start": 158,
          "cds_end": null,
          "cds_length": 369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000673743.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000258461",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*2687_*2690dupGTCA",
          "hgvs_p": null,
          "transcript": "ENST00000495723.1",
          "protein_id": "ENSP00000492063.1",
          "transcript_support_level": 2,
          "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": "ENST00000495723.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000258461",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*2687_*2690dupGTCA",
          "hgvs_p": null,
          "transcript": "ENST00000495723.1",
          "protein_id": "ENSP00000492063.1",
          "transcript_support_level": 2,
          "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": "ENST00000495723.1"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.2233_2236dupGTCA",
          "hgvs_p": "p.Asn746fs",
          "transcript": "NM_024344.2",
          "protein_id": "NP_077320.1",
          "transcript_support_level": null,
          "aa_start": 746,
          "aa_end": null,
          "aa_length": 815,
          "cds_start": 2237,
          "cds_end": null,
          "cds_length": 2448,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024344.2"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.2107_2110dupGTCA",
          "hgvs_p": "p.Asn704fs",
          "transcript": "ENST00000318023.11",
          "protein_id": "ENSP00000326281.8",
          "transcript_support_level": 5,
          "aa_start": 704,
          "aa_end": null,
          "aa_length": 773,
          "cds_start": 2111,
          "cds_end": null,
          "cds_length": 2322,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000318023.11"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.1975_1978dupGTCA",
          "hgvs_p": "p.Asn660fs",
          "transcript": "NM_173087.2",
          "protein_id": "NP_775110.1",
          "transcript_support_level": null,
          "aa_start": 660,
          "aa_end": null,
          "aa_length": 729,
          "cds_start": 1979,
          "cds_end": null,
          "cds_length": 2190,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_173087.2"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.715_718dupGTCA",
          "hgvs_p": "p.Asn240fs",
          "transcript": "NM_173088.2",
          "protein_id": "NP_775111.1",
          "transcript_support_level": null,
          "aa_start": 240,
          "aa_end": null,
          "aa_length": 309,
          "cds_start": 719,
          "cds_end": null,
          "cds_length": 930,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_173088.2"
        },
        {
          "aa_ref": "N",
          "aa_alt": "SQ?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "c.583_586dupGTCA",
          "hgvs_p": "p.Asn196fs",
          "transcript": "ENST00000569827.5",
          "protein_id": "ENSP00000454379.1",
          "transcript_support_level": 5,
          "aa_start": 196,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 587,
          "cds_end": null,
          "cds_length": 767,
          "cdna_start": null,
          "cdna_end": null,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000565274.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "n.*563_*566dupGTCA",
          "hgvs_p": null,
          "transcript": "ENST00000673646.1",
          "protein_id": "ENSP00000501007.1",
          "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": "ENST00000673646.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "n.*322_*325dupGTCA",
          "hgvs_p": null,
          "transcript": "ENST00000673705.1",
          "protein_id": "ENSP00000501021.1",
          "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": "ENST00000673705.1"
        },
        {
          "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": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CAPN3",
          "gene_hgnc_id": 1480,
          "hgvs_c": "n.*319_*320insCAGT",
          "hgvs_p": null,
          "transcript": "ENST00000673893.1",
          "protein_id": "ENSP00000500987.1",
          "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": "ENST00000673893.1"
        }
      ],
      "gene_symbol": "CAPN3",
      "gene_hgnc_id": 1480,
      "dbsnp": "rs398123147",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 7.905,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 12,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 12,
          "benign_score": 0,
          "pathogenic_score": 12,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "NM_000070.3",
          "gene_symbol": "CAPN3",
          "hgnc_id": 1480,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.2251_2254dupGTCA",
          "hgvs_p": "p.Asn752fs"
        },
        {
          "score": 5,
          "benign_score": 0,
          "pathogenic_score": 5,
          "criteria": [
            "PM2",
            "PP3",
            "PP5_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000495723.1",
          "gene_symbol": "ENSG00000258461",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.*2687_*2690dupGTCA",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}