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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 22-30928105-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=30928105&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "22",
      "pos": 30928105,
      "ref": "T",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000397641.8",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2944A>C",
          "hgvs_p": "p.Thr982Pro",
          "transcript": "NM_001303256.3",
          "protein_id": "NP_001290185.1",
          "transcript_support_level": null,
          "aa_start": 982,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": 2944,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": 3829,
          "cdna_end": null,
          "cdna_length": 5657,
          "mane_select": "ENST00000397641.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2944A>C",
          "hgvs_p": "p.Thr982Pro",
          "transcript": "ENST00000397641.8",
          "protein_id": "ENSP00000380763.2",
          "transcript_support_level": 5,
          "aa_start": 982,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": 2944,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": 3829,
          "cdna_end": null,
          "cdna_length": 5657,
          "mane_select": "NM_001303256.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2758A>C",
          "hgvs_p": "p.Thr920Pro",
          "transcript": "ENST00000215862.8",
          "protein_id": "ENSP00000215862.4",
          "transcript_support_level": 1,
          "aa_start": 920,
          "aa_end": null,
          "aa_length": 970,
          "cds_start": 2758,
          "cds_end": null,
          "cds_length": 2913,
          "cdna_start": 4122,
          "cdna_end": null,
          "cdna_length": 4469,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2944A>C",
          "hgvs_p": "p.Thr982Pro",
          "transcript": "NM_001303257.2",
          "protein_id": "NP_001290186.1",
          "transcript_support_level": null,
          "aa_start": 982,
          "aa_end": null,
          "aa_length": 1029,
          "cds_start": 2944,
          "cds_end": null,
          "cds_length": 3090,
          "cdna_start": 3342,
          "cdna_end": null,
          "cdna_length": 5161,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2758A>C",
          "hgvs_p": "p.Thr920Pro",
          "transcript": "NM_014941.3",
          "protein_id": "NP_055756.1",
          "transcript_support_level": null,
          "aa_start": 920,
          "aa_end": null,
          "aa_length": 970,
          "cds_start": 2758,
          "cds_end": null,
          "cds_length": 2913,
          "cdna_start": 4208,
          "cdna_end": null,
          "cdna_length": 6036,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.427A>C",
          "hgvs_p": "p.Thr143Pro",
          "transcript": "ENST00000445980.5",
          "protein_id": "ENSP00000402602.1",
          "transcript_support_level": 5,
          "aa_start": 143,
          "aa_end": null,
          "aa_length": 190,
          "cds_start": 427,
          "cds_end": null,
          "cds_length": 573,
          "cdna_start": 428,
          "cdna_end": null,
          "cdna_length": 766,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2959A>C",
          "hgvs_p": "p.Thr987Pro",
          "transcript": "XM_011530004.3",
          "protein_id": "XP_011528306.1",
          "transcript_support_level": null,
          "aa_start": 987,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": 2959,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": 3844,
          "cdna_end": null,
          "cdna_length": 5672,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2959A>C",
          "hgvs_p": "p.Thr987Pro",
          "transcript": "XM_017028667.3",
          "protein_id": "XP_016884156.1",
          "transcript_support_level": null,
          "aa_start": 987,
          "aa_end": null,
          "aa_length": 1034,
          "cds_start": 2959,
          "cds_end": null,
          "cds_length": 3105,
          "cdna_start": 3844,
          "cdna_end": null,
          "cdna_length": 5663,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2758A>C",
          "hgvs_p": "p.Thr920Pro",
          "transcript": "XM_047441203.1",
          "protein_id": "XP_047297159.1",
          "transcript_support_level": null,
          "aa_start": 920,
          "aa_end": null,
          "aa_length": 970,
          "cds_start": 2758,
          "cds_end": null,
          "cds_length": 2913,
          "cdna_start": 3939,
          "cdna_end": null,
          "cdna_length": 5767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "T",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "c.2758A>C",
          "hgvs_p": "p.Thr920Pro",
          "transcript": "XM_047441204.1",
          "protein_id": "XP_047297160.1",
          "transcript_support_level": null,
          "aa_start": 920,
          "aa_end": null,
          "aa_length": 970,
          "cds_start": 2758,
          "cds_end": null,
          "cds_length": 2913,
          "cdna_start": 4098,
          "cdna_end": null,
          "cdna_length": 5926,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.124A>C",
          "hgvs_p": null,
          "transcript": "ENST00000429468.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 462,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.4390A>C",
          "hgvs_p": null,
          "transcript": "ENST00000674576.1",
          "protein_id": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.629A>C",
          "hgvs_p": null,
          "transcript": "ENST00000674585.1",
          "protein_id": null,
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          "cds_start": -4,
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          "cdna_length": 865,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.334A>C",
          "hgvs_p": null,
          "transcript": "ENST00000675027.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "aa_length": null,
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          "cdna_length": 1706,
          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "MORC2",
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          "hgvs_c": "n.1365A>C",
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          "transcript": "ENST00000675317.1",
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.576A>C",
          "hgvs_p": null,
          "transcript": "ENST00000675402.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_length": 923,
          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.*697A>C",
          "hgvs_p": null,
          "transcript": "ENST00000675570.1",
          "protein_id": "ENSP00000502691.1",
          "transcript_support_level": null,
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          "cdna_length": 1036,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.2786A>C",
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          "transcript": "ENST00000675601.1",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.292A>C",
          "hgvs_p": null,
          "transcript": "ENST00000675779.1",
          "protein_id": "ENSP00000502216.1",
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          "cdna_length": 811,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.696A>C",
          "hgvs_p": null,
          "transcript": "ENST00000675798.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 1043,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MORC2",
          "gene_hgnc_id": 23573,
          "hgvs_c": "n.3787A>C",
          "hgvs_p": null,
          "transcript": "ENST00000676215.1",
          "protein_id": null,
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        {
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        {
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        },
        {
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      ],
      "gene_symbol": "MORC2",
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      "dbsnp": "rs771410096",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.06293275952339172,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.042,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.355,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.51,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.847,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
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          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000397641.8",
          "gene_symbol": "MORC2",
          "hgnc_id": 23573,
          "effects": [
            "missense_variant"
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          "inheritance_mode": "AD",
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          "hgvs_p": "p.Thr982Pro"
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        {
          "score": -2,
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          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000441558.1",
          "gene_symbol": "MORC2-AS1",
          "hgnc_id": 26662,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.68-1772T>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
}