← Back to variant description

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: 15-68229523-C-CCCG (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=68229523&ref=C&alt=CCCG&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 68229523,
      "ref": "C",
      "alt": "CCCG",
      "effect": "conservative_inframe_insertion",
      "transcript": "ENST00000249806.11",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "NM_017882.3",
          "protein_id": "NP_060352.1",
          "transcript_support_level": null,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 311,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 936,
          "cdna_start": 205,
          "cdna_end": null,
          "cdna_length": 2228,
          "mane_select": "ENST00000249806.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000249806.11",
          "protein_id": "ENSP00000249806.5",
          "transcript_support_level": 1,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 311,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 936,
          "cdna_start": 205,
          "cdna_end": null,
          "cdna_length": 2228,
          "mane_select": "NM_017882.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000637667.1",
          "protein_id": "ENSP00000489843.1",
          "transcript_support_level": 1,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 250,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 755,
          "cdna_start": 180,
          "cdna_end": null,
          "cdna_length": 874,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000566347.5",
          "protein_id": "ENSP00000457783.1",
          "transcript_support_level": 1,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 248,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 747,
          "cdna_start": 195,
          "cdna_end": null,
          "cdna_length": 981,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000260007",
          "gene_hgnc_id": null,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000562767.2",
          "protein_id": "ENSP00000456336.1",
          "transcript_support_level": 3,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 92,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 279,
          "cdna_start": 195,
          "cdna_end": null,
          "cdna_length": 3389,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000638076.1",
          "protein_id": "ENSP00000490373.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2323,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000637494.1",
          "protein_id": "ENSP00000490057.1",
          "transcript_support_level": 5,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 215,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 648,
          "cdna_start": 154,
          "cdna_end": null,
          "cdna_length": 765,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000564752.1",
          "protein_id": "ENSP00000457822.1",
          "transcript_support_level": 3,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 213,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 642,
          "cdna_start": 186,
          "cdna_end": null,
          "cdna_length": 900,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000565471.6",
          "protein_id": "ENSP00000457384.1",
          "transcript_support_level": 2,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 158,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 477,
          "cdna_start": 149,
          "cdna_end": null,
          "cdna_length": 1075,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "AG",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_insertion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla",
          "transcript": "ENST00000636314.1",
          "protein_id": "ENSP00000490295.1",
          "transcript_support_level": 3,
          "aa_start": 21,
          "aa_end": null,
          "aa_length": 103,
          "cds_start": 61,
          "cds_end": null,
          "cds_length": 312,
          "cdna_start": 177,
          "cdna_end": null,
          "cdna_length": 442,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000567060.5",
          "protein_id": "ENSP00000454818.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 945,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.193_194insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636020.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 894,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636212.1",
          "protein_id": "ENSP00000489851.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1053,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000260007",
          "gene_hgnc_id": null,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637054.1",
          "protein_id": "ENSP00000490807.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3238,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637450.1",
          "protein_id": "ENSP00000490204.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 868,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000260007",
          "gene_hgnc_id": null,
          "hgvs_c": "n.61_62insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637888.1",
          "protein_id": "ENSP00000490546.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2941,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.180-10874_180-10873insCGG",
          "hgvs_p": null,
          "transcript": "NM_001411068.1",
          "protein_id": "NP_001397997.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 343,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1032,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2523,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "c.180-10874_180-10873insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000538696.5",
          "protein_id": "ENSP00000445770.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 343,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1032,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1343,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.41-15136_41-15135insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000563917.2",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 557,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.516-10874_516-10873insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000564846.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1762,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.173-10874_173-10873insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000635747.1",
          "protein_id": "ENSP00000490627.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1181,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.*104-10874_*104-10873insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000636876.1",
          "protein_id": "ENSP00000489950.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 655,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.173-10874_173-10873insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637223.1",
          "protein_id": "ENSP00000490010.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 652,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.31-15136_31-15135insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000638144.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 576,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLN6",
          "gene_hgnc_id": 2077,
          "hgvs_c": "n.-15_-14insCGG",
          "hgvs_p": null,
          "transcript": "ENST00000637823.1",
          "protein_id": "ENSP00000490011.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 717,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CLN6",
      "gene_hgnc_id": 2077,
      "dbsnp": "rs878855040",
      "frequency_reference_population": 0.000008179168,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 12,
      "gnomad_exomes_af": 0.00000836406,
      "gnomad_genomes_af": 0.00000657929,
      "gnomad_exomes_ac": 11,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "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": 0.36,
      "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": 3,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PM4_Supporting",
      "acmg_by_gene": [
        {
          "score": 3,
          "benign_score": 0,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PM4_Supporting"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000249806.11",
          "gene_symbol": "CLN6",
          "hgnc_id": 2077,
          "effects": [
            "conservative_inframe_insertion"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla"
        },
        {
          "score": 3,
          "benign_score": 0,
          "pathogenic_score": 3,
          "criteria": [
            "PM2",
            "PM4_Supporting"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000562767.2",
          "gene_symbol": "ENSG00000260007",
          "hgnc_id": null,
          "effects": [
            "conservative_inframe_insertion"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.61_62insCGG",
          "hgvs_p": "p.Leu20_Gly21insAla"
        }
      ],
      "clinvar_disease": "Neuronal ceroid lipofuscinosis",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "Neuronal ceroid lipofuscinosis",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}