← 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: 20-63678161-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=63678161&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 21,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1",
            "BS2"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "RTEL1",
          "hgnc_id": 15888,
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "inheritance_mode": "AD,SD,AR",
          "pathogenic_score": 0,
          "score": -21,
          "transcript": "NM_001283009.2",
          "verdict": "Benign"
        },
        {
          "benign_score": 16,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "gene_symbol": "RTEL1-TNFRSF6B",
          "hgnc_id": 44095,
          "hgvs_c": "n.936G>A",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": -16,
          "transcript": "ENST00000492259.6",
          "verdict": "Benign"
        },
        {
          "benign_score": 16,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "gene_symbol": "LOC124904954",
          "hgnc_id": null,
          "hgvs_c": "n.215C>T",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": -16,
          "transcript": "XR_007067717.1",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
      "acmg_score": -21,
      "allele_count_reference_population": 18508,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.57,
      "chr": "20",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_disease": " 3, Telomere-related, autosomal recessive 5,Dyskeratosis congenita,Pulmonary fibrosis and/or bone marrow failure,not provided",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2 B:3",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.5699999928474426,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1300,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4615,
          "cdna_start": 1261,
          "cds_end": null,
          "cds_length": 3903,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "NM_001283009.2",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000360203.11",
          "protein_coding": true,
          "protein_id": "NP_001269938.1",
          "strand": true,
          "transcript": "NM_001283009.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1300,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4615,
          "cdna_start": 1261,
          "cds_end": null,
          "cds_length": 3903,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000360203.11",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001283009.2",
          "protein_coding": true,
          "protein_id": "ENSP00000353332.5",
          "strand": true,
          "transcript": "ENST00000360203.11",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1243,
          "aa_ref": "L",
          "aa_start": 336,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4517,
          "cdna_start": 1333,
          "cds_end": null,
          "cds_length": 3732,
          "cds_start": 1008,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000508582.7",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.1008G>A",
          "hgvs_p": "p.Leu336Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000424307.2",
          "strand": true,
          "transcript": "ENST00000508582.7",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1219,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4955,
          "cdna_start": 1763,
          "cds_end": null,
          "cds_length": 3660,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000370018.7",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000359035.3",
          "strand": true,
          "transcript": "ENST00000370018.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 4824,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 35,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000492259.6",
          "gene_hgnc_id": 44095,
          "gene_symbol": "RTEL1-TNFRSF6B",
          "hgvs_c": "n.936G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000457428.1",
          "strand": true,
          "transcript": "ENST00000492259.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1329,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4697,
          "cdna_start": 1260,
          "cds_end": null,
          "cds_length": 3990,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000962502.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632561.1",
          "strand": true,
          "transcript": "ENST00000962502.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1311,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4638,
          "cdna_start": 1251,
          "cds_end": null,
          "cds_length": 3936,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000962501.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632560.1",
          "strand": true,
          "transcript": "ENST00000962501.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1306,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4648,
          "cdna_start": 1278,
          "cds_end": null,
          "cds_length": 3921,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935990.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606049.1",
          "strand": true,
          "transcript": "ENST00000935990.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1300,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4553,
          "cdna_start": 1196,
          "cds_end": null,
          "cds_length": 3903,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000897317.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000567376.1",
          "strand": true,
          "transcript": "ENST00000897317.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1300,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4629,
          "cdna_start": 1272,
          "cds_end": null,
          "cds_length": 3903,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935985.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606044.1",
          "strand": true,
          "transcript": "ENST00000935985.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1300,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5054,
          "cdna_start": 1700,
          "cds_end": null,
          "cds_length": 3903,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000935993.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606052.1",
          "strand": true,
          "transcript": "ENST00000935993.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1295,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4619,
          "cdna_start": 1279,
          "cds_end": null,
          "cds_length": 3888,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935987.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606046.1",
          "strand": true,
          "transcript": "ENST00000935987.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1295,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4611,
          "cdna_start": 1272,
          "cds_end": null,
          "cds_length": 3888,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935988.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606047.1",
          "strand": true,
          "transcript": "ENST00000935988.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1286,
          "aa_ref": "L",
          "aa_start": 298,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4591,
          "cdna_start": 1236,
          "cds_end": null,
          "cds_length": 3861,
          "cds_start": 894,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935989.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.894G>A",
          "hgvs_p": "p.Leu298Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606048.1",
          "strand": true,
          "transcript": "ENST00000935989.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1286,
          "aa_ref": "L",
          "aa_start": 298,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4580,
          "cdna_start": 1223,
          "cds_end": null,
          "cds_length": 3861,
          "cds_start": 894,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935991.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.894G>A",
          "hgvs_p": "p.Leu298Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606050.1",
          "strand": true,
          "transcript": "ENST00000935991.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1281,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4546,
          "cdna_start": 1251,
          "cds_end": null,
          "cds_length": 3846,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000935992.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606051.1",
          "strand": true,
          "transcript": "ENST00000935992.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1267,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4468,
          "cdna_start": 1210,
          "cds_end": null,
          "cds_length": 3804,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000897316.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000567375.1",
          "strand": true,
          "transcript": "ENST00000897316.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1243,
          "aa_ref": "L",
          "aa_start": 336,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4517,
          "cdna_start": 1333,
          "cds_end": null,
          "cds_length": 3732,
          "cds_start": 1008,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "NM_032957.5",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.1008G>A",
          "hgvs_p": "p.Leu336Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_116575.3",
          "strand": true,
          "transcript": "NM_032957.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1222,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4370,
          "cdna_start": 1249,
          "cds_end": null,
          "cds_length": 3669,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000962503.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632562.1",
          "strand": true,
          "transcript": "ENST00000962503.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 1219,
          "aa_ref": "L",
          "aa_start": 312,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4445,
          "cdna_start": 1261,
          "cds_end": null,
          "cds_length": 3660,
          "cds_start": 936,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 35,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "NM_016434.4",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.936G>A",
          "hgvs_p": "p.Leu312Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_057518.1",
          "strand": true,
          "transcript": "NM_016434.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 996,
          "aa_ref": "L",
          "aa_start": 89,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4676,
          "cdna_start": 1484,
          "cds_end": null,
          "cds_length": 2991,
          "cds_start": 267,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "NM_001283010.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.267G>A",
          "hgvs_p": "p.Leu89Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001269939.1",
          "strand": true,
          "transcript": "NM_001283010.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "L",
          "aa_end": null,
          "aa_length": 996,
          "aa_ref": "L",
          "aa_start": 89,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4162,
          "cdna_start": 980,
          "cds_end": null,
          "cds_length": 2991,
          "cds_start": 267,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 10,
          "exon_rank_end": null,
          "feature": "ENST00000318100.9",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.267G>A",
          "hgvs_p": "p.Leu89Leu",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000322287.5",
          "strand": true,
          "transcript": "ENST00000318100.9",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1305,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4651,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3918,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 34,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000935986.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.920-53G>A",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606045.1",
          "strand": true,
          "transcript": "ENST00000935986.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1305,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4642,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3918,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 34,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000962500.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "c.920-53G>A",
          "hgvs_p": null,
          "intron_rank": 10,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632559.1",
          "strand": true,
          "transcript": "ENST00000962500.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2012,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 23,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000425905.7",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.610G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000425905.7",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3474,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 32,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000482936.6",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.936G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000457868.2",
          "strand": true,
          "transcript": "ENST00000482936.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1714,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 14,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000684971.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513449.1",
          "strand": true,
          "transcript": "ENST00000684971.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2398,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 12,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000686756.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.1254G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000686756.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1891,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 22,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000687123.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513450.1",
          "strand": true,
          "transcript": "ENST00000687123.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1859,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 12,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000692658.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513448.1",
          "strand": true,
          "transcript": "ENST00000692658.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5772,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 38,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "NR_037882.1",
          "gene_hgnc_id": 44095,
          "gene_symbol": "RTEL1-TNFRSF6B",
          "hgvs_c": "n.1763G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "NR_037882.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1926,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "XR_007067717.1",
          "gene_hgnc_id": null,
          "gene_symbol": "LOC124904954",
          "hgvs_c": "n.215C>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "XR_007067717.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1714,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 14,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000684971.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513449.1",
          "strand": true,
          "transcript": "ENST00000684971.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1891,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 22,
          "exon_rank": 9,
          "exon_rank_end": null,
          "feature": "ENST00000687123.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513450.1",
          "strand": true,
          "transcript": "ENST00000687123.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1859,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 12,
          "exon_rank": 11,
          "exon_rank_end": null,
          "feature": "ENST00000692658.1",
          "gene_hgnc_id": 15888,
          "gene_symbol": "RTEL1",
          "hgvs_c": "n.*712G>A",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000513448.1",
          "strand": true,
          "transcript": "ENST00000692658.1",
          "transcript_support_level": null
        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
      "dbscsnv_ada_score": null,
      "dbsnp": "rs41302954",
      "effect": "synonymous_variant",
      "frequency_reference_population": 0.011466324,
      "gene_hgnc_id": 15888,
      "gene_symbol": "RTEL1",
      "gnomad_exomes_ac": 17066,
      "gnomad_exomes_af": 0.0116746,
      "gnomad_exomes_homalt": 122,
      "gnomad_genomes_ac": 1442,
      "gnomad_genomes_af": 0.00946716,
      "gnomad_genomes_homalt": 11,
      "gnomad_mito_heteroplasmic": null,
      "gnomad_mito_homoplasmic": null,
      "hom_count_reference_population": 133,
      "mitotip_prediction": null,
      "mitotip_score": null,
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "phenotype_combined": "Dyskeratosis congenita|Dyskeratosis congenita, autosomal recessive 5;Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3|not provided",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": -0.023,
      "pos": 63678161,
      "ref": "G",
      "revel_prediction": null,
      "revel_score": null,
      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0.009999999776482582,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "transcript": "NM_001283009.2"
    }
  ]
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.