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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: 7-94588701-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=94588701&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 94588701,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000648936.2",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1285C>T",
          "hgvs_p": "p.Gln429*",
          "transcript": "NM_003919.3",
          "protein_id": "NP_003910.1",
          "transcript_support_level": null,
          "aa_start": 429,
          "aa_end": null,
          "aa_length": 437,
          "cds_start": 1285,
          "cds_end": null,
          "cds_length": 1314,
          "cdna_start": 1320,
          "cdna_end": null,
          "cdna_length": 1868,
          "mane_select": "ENST00000648936.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1285C>T",
          "hgvs_p": "p.Gln429*",
          "transcript": "ENST00000648936.2",
          "protein_id": "ENSP00000497130.1",
          "transcript_support_level": null,
          "aa_start": 429,
          "aa_end": null,
          "aa_length": 437,
          "cds_start": 1285,
          "cds_end": null,
          "cds_length": 1314,
          "cdna_start": 1320,
          "cdna_end": null,
          "cdna_length": 1868,
          "mane_select": "NM_003919.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1237C>T",
          "hgvs_p": "p.Gln413*",
          "transcript": "ENST00000428696.7",
          "protein_id": "ENSP00000397536.3",
          "transcript_support_level": 1,
          "aa_start": 413,
          "aa_end": null,
          "aa_length": 444,
          "cds_start": 1237,
          "cds_end": null,
          "cds_length": 1335,
          "cdna_start": 1244,
          "cdna_end": null,
          "cdna_length": 1368,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1258C>T",
          "hgvs_p": "p.Gln420*",
          "transcript": "ENST00000447873.6",
          "protein_id": "ENSP00000388734.1",
          "transcript_support_level": 1,
          "aa_start": 420,
          "aa_end": null,
          "aa_length": 428,
          "cds_start": 1258,
          "cds_end": null,
          "cds_length": 1287,
          "cdna_start": 1367,
          "cdna_end": null,
          "cdna_length": 1672,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1474C>T",
          "hgvs_p": "p.Gln492*",
          "transcript": "ENST00000647096.1",
          "protein_id": "ENSP00000494192.1",
          "transcript_support_level": null,
          "aa_start": 492,
          "aa_end": null,
          "aa_length": 500,
          "cds_start": 1474,
          "cds_end": null,
          "cds_length": 1503,
          "cdna_start": 1492,
          "cdna_end": null,
          "cdna_length": 1610,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1447C>T",
          "hgvs_p": "p.Gln483*",
          "transcript": "ENST00000645101.1",
          "protein_id": "ENSP00000494975.1",
          "transcript_support_level": null,
          "aa_start": 483,
          "aa_end": null,
          "aa_length": 491,
          "cds_start": 1447,
          "cds_end": null,
          "cds_length": 1476,
          "cdna_start": 1495,
          "cdna_end": null,
          "cdna_length": 1739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1441C>T",
          "hgvs_p": "p.Gln481*",
          "transcript": "ENST00000642707.1",
          "protein_id": "ENSP00000495270.1",
          "transcript_support_level": null,
          "aa_start": 481,
          "aa_end": null,
          "aa_length": 489,
          "cds_start": 1441,
          "cds_end": null,
          "cds_length": 1470,
          "cdna_start": 1479,
          "cdna_end": null,
          "cdna_length": 1713,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1366C>T",
          "hgvs_p": "p.Gln456*",
          "transcript": "ENST00000647351.1",
          "protein_id": "ENSP00000494556.1",
          "transcript_support_level": null,
          "aa_start": 456,
          "aa_end": null,
          "aa_length": 487,
          "cds_start": 1366,
          "cds_end": null,
          "cds_length": 1464,
          "cdna_start": 1394,
          "cdna_end": null,
          "cdna_length": 1977,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1360C>T",
          "hgvs_p": "p.Gln454*",
          "transcript": "ENST00000646943.1",
          "protein_id": "ENSP00000494666.1",
          "transcript_support_level": null,
          "aa_start": 454,
          "aa_end": null,
          "aa_length": 485,
          "cds_start": 1360,
          "cds_end": null,
          "cds_length": 1458,
          "cdna_start": 1388,
          "cdna_end": null,
          "cdna_length": 1667,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1366C>T",
          "hgvs_p": "p.Gln456*",
          "transcript": "ENST00000644122.1",
          "protein_id": "ENSP00000495236.1",
          "transcript_support_level": null,
          "aa_start": 456,
          "aa_end": null,
          "aa_length": 482,
          "cds_start": 1366,
          "cds_end": null,
          "cds_length": 1449,
          "cdna_start": 1473,
          "cdna_end": null,
          "cdna_length": 1779,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1363C>T",
          "hgvs_p": "p.Gln455*",
          "transcript": "ENST00000647334.1",
          "protein_id": "ENSP00000495114.1",
          "transcript_support_level": null,
          "aa_start": 455,
          "aa_end": null,
          "aa_length": 481,
          "cds_start": 1363,
          "cds_end": null,
          "cds_length": 1446,
          "cdna_start": 1364,
          "cdna_end": null,
          "cdna_length": 1554,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1345C>T",
          "hgvs_p": "p.Gln449*",
          "transcript": "ENST00000646265.1",
          "protein_id": "ENSP00000494587.1",
          "transcript_support_level": null,
          "aa_start": 449,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": 1345,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": 1347,
          "cdna_end": null,
          "cdna_length": 1564,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1339C>T",
          "hgvs_p": "p.Gln447*",
          "transcript": "ENST00000642441.1",
          "protein_id": "ENSP00000495994.1",
          "transcript_support_level": null,
          "aa_start": 447,
          "aa_end": null,
          "aa_length": 478,
          "cds_start": 1339,
          "cds_end": null,
          "cds_length": 1437,
          "cdna_start": 1390,
          "cdna_end": null,
          "cdna_length": 1592,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1333C>T",
          "hgvs_p": "p.Gln445*",
          "transcript": "ENST00000644116.1",
          "protein_id": "ENSP00000495276.1",
          "transcript_support_level": null,
          "aa_start": 445,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1333,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1382,
          "cdna_end": null,
          "cdna_length": 1577,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1393C>T",
          "hgvs_p": "p.Gln465*",
          "transcript": "NM_001346713.2",
          "protein_id": "NP_001333642.1",
          "transcript_support_level": null,
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          "cds_start": 1393,
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          "cdna_start": 1428,
          "cdna_end": null,
          "cdna_length": 1976,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1324C>T",
          "hgvs_p": "p.Gln442*",
          "transcript": "ENST00000644375.1",
          "protein_id": "ENSP00000494315.1",
          "transcript_support_level": null,
          "aa_start": 442,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 1324,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 1436,
          "cdna_end": null,
          "cdna_length": 1715,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1393C>T",
          "hgvs_p": "p.Gln465*",
          "transcript": "ENST00000646489.1",
          "protein_id": "ENSP00000496268.1",
          "transcript_support_level": null,
          "aa_start": 465,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 1393,
          "cds_end": null,
          "cds_length": 1422,
          "cdna_start": 1435,
          "cdna_end": null,
          "cdna_length": 1733,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1393C>T",
          "hgvs_p": "p.Gln465*",
          "transcript": "ENST00000415788.3",
          "protein_id": "ENSP00000405313.2",
          "transcript_support_level": 2,
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          "cds_start": 1393,
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          "cds_length": 1416,
          "cdna_start": 1481,
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          "biotype": null,
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        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1366C>T",
          "hgvs_p": "p.Gln456*",
          "transcript": "NM_001346715.2",
          "protein_id": "NP_001333644.1",
          "transcript_support_level": null,
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          "aa_length": 464,
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          "cdna_start": 1401,
          "cdna_end": null,
          "cdna_length": 1949,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
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          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1366C>T",
          "hgvs_p": "p.Gln456*",
          "transcript": "ENST00000643272.1",
          "protein_id": "ENSP00000494488.1",
          "transcript_support_level": null,
          "aa_start": 456,
          "aa_end": null,
          "aa_length": 464,
          "cds_start": 1366,
          "cds_end": null,
          "cds_length": 1395,
          "cdna_start": 1433,
          "cdna_end": null,
          "cdna_length": 1677,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.1366C>T",
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          "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": 5045,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CASD1",
          "gene_hgnc_id": 16014,
          "hgvs_c": "n.2403+34126G>A",
          "hgvs_p": null,
          "transcript": "XR_007060139.1",
          "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": 4519,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CASD1",
          "gene_hgnc_id": 16014,
          "hgvs_c": "n.2403+34126G>A",
          "hgvs_p": null,
          "transcript": "XR_007060140.1",
          "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": 4533,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SGCE",
          "gene_hgnc_id": 10808,
          "hgvs_c": "c.*7C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643020.1",
          "protein_id": "ENSP00000494457.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 400,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1203,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1204,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SGCE",
      "gene_hgnc_id": 10808,
      "dbsnp": "rs371568101",
      "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": 0.6499999761581421,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.23000000417232513,
      "splice_prediction_selected": "Uncertain_significance",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.65,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 6.871,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.23,
      "spliceai_max_prediction": "Uncertain_significance",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate,PM2",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PVS1_Moderate",
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000648936.2",
          "gene_symbol": "SGCE",
          "hgnc_id": 10808,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1285C>T",
          "hgvs_p": "p.Gln429*"
        },
        {
          "score": 6,
          "benign_score": 0,
          "pathogenic_score": 6,
          "criteria": [
            "PM2",
            "PP3_Strong"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "XR_007060138.1",
          "gene_symbol": "CASD1",
          "hgnc_id": 16014,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "n.2403+34126G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}