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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: 19-11447525-AGAGGAGGAGGAGGAGGAG-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=11447525&ref=AGAGGAGGAGGAGGAGGAG&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 11447525,
      "ref": "AGAGGAGGAGGAGGAGGAG",
      "alt": "A",
      "effect": "disruptive_inframe_deletion",
      "transcript": "NM_001289103.2",
      "consequences": [
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "NM_001289104.2",
          "protein_id": "NP_001276033.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000677123.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001289104.2"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000677123.1",
          "protein_id": "ENSP00000503163.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001289104.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000677123.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000592741.5",
          "protein_id": "ENSP00000466134.1",
          "transcript_support_level": 1,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000592741.5"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000589838.5",
          "protein_id": "ENSP00000465461.1",
          "transcript_support_level": 1,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 528,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1587,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000589838.5"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.987_1004delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu330_Glu335del",
          "transcript": "ENST00000951516.1",
          "protein_id": "ENSP00000621575.1",
          "transcript_support_level": null,
          "aa_start": 329,
          "aa_end": null,
          "aa_length": 547,
          "cds_start": 987,
          "cds_end": null,
          "cds_length": 1644,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000951516.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.993_1010delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu332_Glu337del",
          "transcript": "ENST00000852995.1",
          "protein_id": "ENSP00000523054.1",
          "transcript_support_level": null,
          "aa_start": 331,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 993,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852995.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.975_992delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu326_Glu331del",
          "transcript": "ENST00000852993.1",
          "protein_id": "ENSP00000523052.1",
          "transcript_support_level": null,
          "aa_start": 325,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 975,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852993.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "NM_001289103.2",
          "protein_id": "NP_001276032.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001289103.2"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000852989.1",
          "protein_id": "ENSP00000523048.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852989.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000852990.1",
          "protein_id": "ENSP00000523049.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852990.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000852997.1",
          "protein_id": "ENSP00000523056.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852997.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853001.1",
          "protein_id": "ENSP00000523060.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000853001.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853002.1",
          "protein_id": "ENSP00000523061.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000853002.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853003.1",
          "protein_id": "ENSP00000523062.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000853003.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853004.1",
          "protein_id": "ENSP00000523063.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000853004.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853008.1",
          "protein_id": "ENSP00000523067.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1608,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000853008.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000916401.1",
          "protein_id": "ENSP00000586460.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 535,
          "cds_start": 951,
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          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000916401.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "ENST00000853007.1",
          "protein_id": "ENSP00000523066.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 534,
          "cds_start": 951,
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          "cds_length": 1605,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000853007.1"
        },
        {
          "aa_ref": "EEEEEEE",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del",
          "transcript": "NM_001379608.1",
          "protein_id": "NP_001366537.1",
          "transcript_support_level": null,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 528,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1587,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001379608.1"
        },
        {
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          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "n.142_159delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": null,
          "transcript": "ENST00000585540.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": "retained_intron",
          "feature": "ENST00000585540.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "n.198_215delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": null,
          "transcript": "ENST00000592445.1",
          "protein_id": null,
          "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": "retained_intron",
          "feature": "ENST00000592445.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRKCSH",
          "gene_hgnc_id": 9411,
          "hgvs_c": "n.-39_-22delGAGGAGGAGGAGGAGGAG",
          "hgvs_p": null,
          "transcript": "ENST00000586486.1",
          "protein_id": "ENSP00000465948.1",
          "transcript_support_level": 1,
          "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": "ENST00000586486.1"
        }
      ],
      "gene_symbol": "PRKCSH",
      "gene_hgnc_id": 9411,
      "dbsnp": "rs3217229",
      "frequency_reference_population": 0.000006688158,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000668816,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 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": 3.273,
      "phylop100way_prediction": "Benign",
      "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": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP3",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 1,
          "pathogenic_score": 0,
          "criteria": [
            "BP3"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001289103.2",
          "gene_symbol": "PRKCSH",
          "hgnc_id": 9411,
          "effects": [
            "disruptive_inframe_deletion"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.951_968delGGAGGAGGAGGAGGAGGA",
          "hgvs_p": "p.Glu318_Glu323del"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}