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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: 3-47504433-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=47504433&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 47504433,
      "ref": "T",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_001031703.3",
      "consequences": [
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.220A>G",
          "hgvs_p": "p.Met74Val",
          "transcript": "NM_001031703.3",
          "protein_id": "NP_001026873.2",
          "transcript_support_level": null,
          "aa_start": 74,
          "aa_end": null,
          "aa_length": 266,
          "cds_start": 220,
          "cds_end": null,
          "cds_length": 801,
          "cdna_start": 342,
          "cdna_end": null,
          "cdna_length": 1352,
          "mane_select": "ENST00000296149.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.220A>G",
          "hgvs_p": "p.Met74Val",
          "transcript": "ENST00000296149.9",
          "protein_id": "ENSP00000296149.4",
          "transcript_support_level": 1,
          "aa_start": 74,
          "aa_end": null,
          "aa_length": 266,
          "cds_start": 220,
          "cds_end": null,
          "cds_length": 801,
          "cdna_start": 342,
          "cdna_end": null,
          "cdna_length": 1352,
          "mane_select": "NM_001031703.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001363957.1",
          "protein_id": "NP_001350886.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 520,
          "cdna_end": null,
          "cdna_length": 1530,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424220.1",
          "protein_id": "NP_001411149.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 258,
          "cdna_end": null,
          "cdna_length": 1268,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424222.1",
          "protein_id": "NP_001411151.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 449,
          "cdna_end": null,
          "cdna_length": 1459,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424223.1",
          "protein_id": "NP_001411152.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 728,
          "cdna_end": null,
          "cdna_length": 1738,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424224.1",
          "protein_id": "NP_001411153.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 289,
          "cdna_end": null,
          "cdna_length": 1299,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424225.1",
          "protein_id": "NP_001411154.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 377,
          "cdna_end": null,
          "cdna_length": 1387,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424226.1",
          "protein_id": "NP_001411155.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 365,
          "cdna_end": null,
          "cdna_length": 1375,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424227.1",
          "protein_id": "NP_001411156.1",
          "transcript_support_level": null,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 876,
          "cdna_end": null,
          "cdna_length": 1886,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000439305.5",
          "protein_id": "ENSP00000402399.1",
          "transcript_support_level": 2,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
          "cds_end": null,
          "cds_length": 582,
          "cdna_start": 259,
          "cdna_end": null,
          "cdna_length": 880,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000446787.5",
          "protein_id": "ENSP00000412593.1",
          "transcript_support_level": 3,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 193,
          "cds_start": 1,
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          "cds_length": 582,
          "cdna_start": 190,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000412761.5",
          "protein_id": "ENSP00000415301.1",
          "transcript_support_level": 5,
          "aa_start": 1,
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          "aa_length": 156,
          "cds_start": 1,
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          "cdna_start": 233,
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          "cdna_length": 705,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
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          "protein_coding": true,
          "strand": false,
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          ],
          "exon_rank": 4,
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          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000444760.5",
          "protein_id": "ENSP00000406130.1",
          "transcript_support_level": 5,
          "aa_start": 1,
          "aa_end": null,
          "aa_length": 150,
          "cds_start": 1,
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          "cds_length": 453,
          "cdna_start": 556,
          "cdna_end": null,
          "cdna_length": 1008,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "start_lost"
          ],
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          "exon_count": 6,
          "intron_rank": null,
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          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "NM_001424230.1",
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
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          "strand": false,
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          ],
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          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000425291.5",
          "protein_id": "ENSP00000400643.1",
          "transcript_support_level": 2,
          "aa_start": 1,
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          "aa_length": 112,
          "cds_start": 1,
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          "cds_length": 340,
          "cdna_start": 255,
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          "cdna_length": 594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000449409.5",
          "protein_id": "ENSP00000410790.1",
          "transcript_support_level": 3,
          "aa_start": 1,
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          "aa_length": 98,
          "cds_start": 1,
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          "cdna_start": 283,
          "cdna_end": null,
          "cdna_length": 579,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "start_lost"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "ENST00000414236.5",
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          "feature": null
        },
        {
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          "intron_rank": null,
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          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.1A>G",
          "hgvs_p": "p.Met1?",
          "transcript": "XM_047448390.1",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 4,
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          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.220A>G",
          "hgvs_p": "p.Met74Val",
          "transcript": "NM_001424210.1",
          "protein_id": "NP_001411139.1",
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          "aa_length": 274,
          "cds_start": 220,
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          "cds_length": 825,
          "cdna_start": 342,
          "cdna_end": null,
          "cdna_length": 1376,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "c.211A>G",
          "hgvs_p": "p.Met71Val",
          "transcript": "NM_001424211.1",
          "protein_id": "NP_001411140.1",
          "transcript_support_level": null,
          "aa_start": 71,
          "aa_end": null,
          "aa_length": 263,
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          "hgvs_p": null,
          "transcript": "ENST00000494161.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 487,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELP6",
          "gene_hgnc_id": 25976,
          "hgvs_c": "n.342A>G",
          "hgvs_p": null,
          "transcript": "NR_188162.1",
          "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": 1386,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ELP6",
      "gene_hgnc_id": 25976,
      "dbsnp": "rs150166753",
      "frequency_reference_population": 0.00009141211,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 147,
      "gnomad_exomes_af": 0.0000941053,
      "gnomad_genomes_af": 0.0000656659,
      "gnomad_exomes_ac": 137,
      "gnomad_genomes_ac": 10,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.03182908892631531,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.065,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0519,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.48,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.382,
      "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": -6,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate",
      "acmg_by_gene": [
        {
          "score": -6,
          "benign_score": 6,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001031703.3",
          "gene_symbol": "ELP6",
          "hgnc_id": 25976,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.220A>G",
          "hgvs_p": "p.Met74Val"
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}