← 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: 2-1844538-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=1844538&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 1844538,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000647738.2",
      "consequences": [
        {
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001303052.2",
          "protein_id": "NP_001289981.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7144,
          "mane_select": "ENST00000647738.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647738.2",
          "protein_id": "ENSP00000497479.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7144,
          "mane_select": "NM_001303052.2",
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000428368.7",
          "protein_id": "ENSP00000396103.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6951,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000399161.8",
          "protein_id": "ENSP00000382114.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7227,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000644820.1",
          "protein_id": "ENSP00000496210.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7269,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329844.2",
          "protein_id": "NP_001316773.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7220,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329845.1",
          "protein_id": "NP_001316774.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7010,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647694.1",
          "protein_id": "ENSP00000497722.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6804,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000650485.2",
          "protein_id": "ENSP00000497068.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7178,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2772-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000650560.1",
          "protein_id": "ENSP00000497816.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1185,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3558,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7067,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329847.2",
          "protein_id": "NP_001316776.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7105,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329848.1",
          "protein_id": "NP_001316777.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7187,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_015025.4",
          "protein_id": "NP_055840.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7138,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648316.1",
          "protein_id": "ENSP00000497870.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6912,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648928.1",
          "protein_id": "ENSP00000497017.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7322,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000649207.1",
          "protein_id": "ENSP00000496986.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7009,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329849.3",
          "protein_id": "NP_001316778.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6376,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648665.2",
          "protein_id": "ENSP00000497115.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6155,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329846.3",
          "protein_id": "NP_001316775.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1146,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3441,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6337,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647755.1",
          "protein_id": "ENSP00000496922.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1146,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3441,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6259,
          "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": 24,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329851.3",
          "protein_id": "NP_001316780.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1143,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3432,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7434,
          "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": 24,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "NM_001329852.3",
          "protein_id": "NP_001316781.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1143,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3432,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7401,
          "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": 24,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648318.1",
          "protein_id": "ENSP00000496831.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1143,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3432,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7273,
          "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": 24,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648339.1",
          "protein_id": "ENSP00000497493.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1143,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3432,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7299,
          "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": 24,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000649663.1",
          "protein_id": "ENSP00000497273.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1143,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3432,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7192,
          "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": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2712-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647618.1",
          "protein_id": "ENSP00000497024.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1127,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3384,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6336,
          "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": 16,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2268-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648753.2",
          "protein_id": "ENSP00000497206.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 981,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2946,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4927,
          "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": 15,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2262-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648931.2",
          "protein_id": "ENSP00000498210.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 972,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2919,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5916,
          "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": 15,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2325-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648943.2",
          "protein_id": "ENSP00000496971.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 941,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2826,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2828,
          "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": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.1797-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648933.1",
          "protein_id": "ENSP00000497838.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 860,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6094,
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2268-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648430.2",
          "protein_id": "ENSP00000497371.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 858,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2577,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3751,
          "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": 24,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.1797-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648627.1",
          "protein_id": "ENSP00000497309.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 824,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2475,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5368,
          "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": 15,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.1248-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000650399.2",
          "protein_id": "ENSP00000497900.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4753,
          "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": 14,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.1221-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000649840.2",
          "protein_id": "ENSP00000496783.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 668,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2007,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4737,
          "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": 12,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.741-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000649092.2",
          "protein_id": "ENSP00000497331.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3617,
          "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": 16,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.*665-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000647687.2",
          "protein_id": "ENSP00000498070.2",
          "transcript_support_level": null,
          "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": 4846,
          "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": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.1580-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648299.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 4992,
          "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": 14,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.1147-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648465.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 4653,
          "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": 13,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.1273-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648478.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 4021,
          "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": 14,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.1272-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648643.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 4792,
          "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": 10,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.*90-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648885.2",
          "protein_id": "ENSP00000497348.2",
          "transcript_support_level": null,
          "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": 1334,
          "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": 11,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "n.865-3695T>C",
          "hgvs_p": null,
          "transcript": "ENST00000648913.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 4359,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000307932",
          "gene_hgnc_id": null,
          "hgvs_c": "n.339+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000829894.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 761,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000307932",
          "gene_hgnc_id": null,
          "hgvs_c": "n.339+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000829895.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 506,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510318.2",
          "protein_id": "XP_011508620.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7213,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510319.2",
          "protein_id": "XP_011508621.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7180,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510320.4",
          "protein_id": "XP_011508622.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7262,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510321.3",
          "protein_id": "XP_011508623.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7079,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510322.3",
          "protein_id": "XP_011508624.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7097,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510323.1",
          "protein_id": "XP_011508625.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7036,
          "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": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003604.2",
          "protein_id": "XP_016859093.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7289,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003605.2",
          "protein_id": "XP_016859094.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6964,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510324.3",
          "protein_id": "XP_011508626.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7207,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2832-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003606.2",
          "protein_id": "XP_016859095.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7174,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2832-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003607.3",
          "protein_id": "XP_016859096.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7256,
          "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": 23,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003608.2",
          "protein_id": "XP_016859097.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1198,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10490,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510326.2",
          "protein_id": "XP_011508628.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1188,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3567,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7150,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2769-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003612.2",
          "protein_id": "XP_016859101.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1186,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3561,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7111,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510327.2",
          "protein_id": "XP_011508629.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1171,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3516,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6445,
          "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": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2838-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_011510328.3",
          "protein_id": "XP_011508630.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1169,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3510,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6439,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003615.2",
          "protein_id": "XP_016859104.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1150,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3453,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6382,
          "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": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003616.2",
          "protein_id": "XP_016859105.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6376,
          "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": 19,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "MYT1L",
          "gene_hgnc_id": 7623,
          "hgvs_c": "c.2544-3695T>C",
          "hgvs_p": null,
          "transcript": "XM_017003620.1",
          "protein_id": "XP_016859109.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1111,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3336,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6303,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "LOC107985838",
          "gene_hgnc_id": null,
          "hgvs_c": "n.321+3A>G",
          "hgvs_p": null,
          "transcript": "XR_007086190.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 442,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "LOC107985838",
          "gene_hgnc_id": null,
          "hgvs_c": "n.321+3A>G",
          "hgvs_p": null,
          "transcript": "XR_007086191.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 388,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MYT1L",
      "gene_hgnc_id": 7623,
      "dbsnp": "rs11127313",
      "frequency_reference_population": 0.4403266,
      "hom_count_reference_population": 15644,
      "allele_count_reference_population": 66927,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.440327,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 66927,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 15644,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -1.0099999904632568,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -1.01,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.679,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000647738.2",
          "gene_symbol": "MYT1L",
          "hgnc_id": 7623,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2775-3695T>C",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000829894.1",
          "gene_symbol": "ENSG00000307932",
          "hgnc_id": null,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.339+3A>G",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "XR_007086190.1",
          "gene_symbol": "LOC107985838",
          "hgnc_id": null,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.321+3A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}