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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: 16-29812298-GGAGCTGTCCGGAGGCCGGCGTCGAGGTGA-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=29812298&ref=GGAGCTGTCCGGAGGCCGGCGTCGAGGTGA&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 29812298,
      "ref": "GGAGCTGTCCGGAGGCCGGCGTCGAGGTGA",
      "alt": "G",
      "effect": "splice_donor_variant,splice_region_variant,5_prime_UTR_variant,intron_variant",
      "transcript": "NM_001256442.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_145239.3",
          "protein_id": "NP_660282.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000358758.12",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_145239.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000358758.12",
          "protein_id": "ENSP00000351608.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_145239.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358758.12"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_145239.3",
          "protein_id": "NP_660282.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000358758.12",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_145239.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000358758.12",
          "protein_id": "ENSP00000351608.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_145239.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358758.12"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_145239.3",
          "protein_id": "NP_660282.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000358758.12",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_145239.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "non_coding_transcript_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000358758.12",
          "protein_id": "ENSP00000351608.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_145239.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358758.12"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000280893",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000609618.2",
          "protein_id": "ENSP00000476774.2",
          "transcript_support_level": 5,
          "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": "ENST00000609618.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000280893",
          "gene_hgnc_id": null,
          "hgvs_c": "n.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000609618.2",
          "protein_id": "ENSP00000476774.2",
          "transcript_support_level": 5,
          "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": "ENST00000609618.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_001256442.2",
          "protein_id": "NP_001243371.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 394,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1185,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001256442.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000567659.3",
          "protein_id": "ENSP00000456226.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 394,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1185,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000567659.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_001438122.1",
          "protein_id": "NP_001425051.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001438122.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000647876.1",
          "protein_id": "ENSP00000498021.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 299,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 900,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000647876.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000636619.1",
          "protein_id": "ENSP00000489669.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 287,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 864,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636619.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000637403.1",
          "protein_id": "ENSP00000489782.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 286,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 861,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000637403.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000637565.1",
          "protein_id": "ENSP00000490207.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 155,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 468,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000637565.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "ENST00000567551.2",
          "protein_id": "ENSP00000489813.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 144,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 436,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000567551.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "XM_017022887.3",
          "protein_id": "XP_016878376.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 346,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1041,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_017022887.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "XM_017022889.3",
          "protein_id": "XP_016878378.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_017022889.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-116_-88delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null,
          "transcript": "NM_001438121.1",
          "protein_id": "NP_001425050.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 394,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1185,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001438121.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
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        {
          "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": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "MVP-DT",
          "gene_hgnc_id": 56029,
          "hgvs_c": "n.247-2154_247-2126delTCACCTCGACGCCGGCCTCCGGACAGCTC",
          "hgvs_p": null,
          "transcript": "NR_186424.1",
          "protein_id": null,
          "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": "pseudogene",
          "feature": "NR_186424.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-171_-143delGAGCTGTCCGGAGGCCGGCGTCGAGGTGA",
          "hgvs_p": null,
          "transcript": "ENST00000637064.1",
          "protein_id": "ENSP00000490826.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1023,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000637064.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PRRT2",
          "gene_hgnc_id": 30500,
          "hgvs_c": "c.-239_-211delGAGCTGTCCGGAGGCCGGCGTCGAGGTGA",
          "hgvs_p": null,
          "transcript": "ENST00000636246.1",
          "protein_id": "ENSP00000489948.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 117,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 354,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000636246.1"
        },
        {
          "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": "ENSG00000280607",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*72_*100delGAGCTGTCCGGAGGCCGGCGTCGAGGTGA",
          "hgvs_p": null,
          "transcript": "ENST00000562594.2",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": "pseudogene",
          "feature": "ENST00000562594.2"
        }
      ],
      "gene_symbol": "PRRT2",
      "gene_hgnc_id": 30500,
      "dbsnp": "rs1555502431",
      "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": 1.689,
      "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": 6,
      "acmg_classification": "Likely_pathogenic",
      "acmg_criteria": "PVS1,BP6_Moderate",
      "acmg_by_gene": [
        {
          "score": 6,
          "benign_score": 2,
          "pathogenic_score": 8,
          "criteria": [
            "PVS1",
            "BP6_Moderate"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "NM_001256442.2",
          "gene_symbol": "PRRT2",
          "hgnc_id": 30500,
          "effects": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000609618.2",
          "gene_symbol": "ENSG00000280893",
          "hgnc_id": null,
          "effects": [
            "splice_donor_variant",
            "splice_region_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-88_-66+6delGCTGTCCGGAGGCCGGCGTCGAGGTGAGA",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000569039.5",
          "gene_symbol": "MVP-DT",
          "hgnc_id": 56029,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.246-2154_246-2126delTCACCTCGACGCCGGCCTCCGGACAGCTC",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000562594.2",
          "gene_symbol": "ENSG00000280607",
          "hgnc_id": null,
          "effects": [
            "downstream_gene_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.*72_*100delGAGCTGTCCGGAGGCCGGCGTCGAGGTGA",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}