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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: 11-9787654-CTTT-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=9787654&ref=CTTT&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 9787654,
      "ref": "CTTT",
      "alt": "C",
      "effect": "conservative_inframe_deletion",
      "transcript": "ENST00000256190.13",
      "consequences": [
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5014_5016delAAA",
          "hgvs_p": "p.Lys1672del",
          "transcript": "NM_030962.4",
          "protein_id": "NP_112224.1",
          "transcript_support_level": null,
          "aa_start": 1672,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 5014,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 5166,
          "cdna_end": null,
          "cdna_length": 7450,
          "mane_select": "ENST00000256190.13",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5014_5016delAAA",
          "hgvs_p": "p.Lys1672del",
          "transcript": "ENST00000256190.13",
          "protein_id": "ENSP00000256190.8",
          "transcript_support_level": 1,
          "aa_start": 1672,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 5014,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 5166,
          "cdna_end": null,
          "cdna_length": 7450,
          "mane_select": "NM_030962.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5110_5112delAAA",
          "hgvs_p": "p.Lys1704del",
          "transcript": "NM_001386339.1",
          "protein_id": "NP_001373268.1",
          "transcript_support_level": null,
          "aa_start": 1704,
          "aa_end": null,
          "aa_length": 1881,
          "cds_start": 5110,
          "cds_end": null,
          "cds_length": 5646,
          "cdna_start": 5262,
          "cdna_end": null,
          "cdna_length": 7546,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5110_5112delAAA",
          "hgvs_p": "p.Lys1704del",
          "transcript": "ENST00000689128.1",
          "protein_id": "ENSP00000509587.1",
          "transcript_support_level": null,
          "aa_start": 1704,
          "aa_end": null,
          "aa_length": 1881,
          "cds_start": 5110,
          "cds_end": null,
          "cds_length": 5646,
          "cdna_start": 5171,
          "cdna_end": null,
          "cdna_length": 7279,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5089_5091delAAA",
          "hgvs_p": "p.Lys1697del",
          "transcript": "ENST00000675281.2",
          "protein_id": "ENSP00000502491.1",
          "transcript_support_level": null,
          "aa_start": 1697,
          "aa_end": null,
          "aa_length": 1874,
          "cds_start": 5089,
          "cds_end": null,
          "cds_length": 5625,
          "cdna_start": 5241,
          "cdna_end": null,
          "cdna_length": 7347,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5071_5073delAAA",
          "hgvs_p": "p.Lys1691del",
          "transcript": "ENST00000676387.2",
          "protein_id": "ENSP00000502779.1",
          "transcript_support_level": null,
          "aa_start": 1691,
          "aa_end": null,
          "aa_length": 1868,
          "cds_start": 5071,
          "cds_end": null,
          "cds_length": 5607,
          "cdna_start": 5211,
          "cdna_end": null,
          "cdna_length": 7167,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5050_5052delAAA",
          "hgvs_p": "p.Lys1684del",
          "transcript": "NM_001424318.1",
          "protein_id": "NP_001411247.1",
          "transcript_support_level": null,
          "aa_start": 1684,
          "aa_end": null,
          "aa_length": 1861,
          "cds_start": 5050,
          "cds_end": null,
          "cds_length": 5586,
          "cdna_start": 5596,
          "cdna_end": null,
          "cdna_length": 7880,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5050_5052delAAA",
          "hgvs_p": "p.Lys1684del",
          "transcript": "NM_001425070.1",
          "protein_id": "NP_001411999.1",
          "transcript_support_level": null,
          "aa_start": 1684,
          "aa_end": null,
          "aa_length": 1861,
          "cds_start": 5050,
          "cds_end": null,
          "cds_length": 5586,
          "cdna_start": 5396,
          "cdna_end": null,
          "cdna_length": 7680,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.5008_5010delAAA",
          "hgvs_p": "p.Lys1670del",
          "transcript": "ENST00000689940.1",
          "protein_id": "ENSP00000508452.1",
          "transcript_support_level": null,
          "aa_start": 1670,
          "aa_end": null,
          "aa_length": 1847,
          "cds_start": 5008,
          "cds_end": null,
          "cds_length": 5544,
          "cdna_start": 5168,
          "cdna_end": null,
          "cdna_length": 7452,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4951_4953delAAA",
          "hgvs_p": "p.Lys1651del",
          "transcript": "ENST00000689258.1",
          "protein_id": "ENSP00000510475.1",
          "transcript_support_level": null,
          "aa_start": 1651,
          "aa_end": null,
          "aa_length": 1828,
          "cds_start": 4951,
          "cds_end": null,
          "cds_length": 5487,
          "cdna_start": 5094,
          "cdna_end": null,
          "cdna_length": 6667,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4909_4911delAAA",
          "hgvs_p": "p.Lys1637del",
          "transcript": "NM_001425069.1",
          "protein_id": "NP_001411998.1",
          "transcript_support_level": null,
          "aa_start": 1637,
          "aa_end": null,
          "aa_length": 1814,
          "cds_start": 4909,
          "cds_end": null,
          "cds_length": 5445,
          "cdna_start": 5255,
          "cdna_end": null,
          "cdna_length": 7539,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4885_4887delAAA",
          "hgvs_p": "p.Lys1629del",
          "transcript": "NM_001386342.1",
          "protein_id": "NP_001373271.1",
          "transcript_support_level": null,
          "aa_start": 1629,
          "aa_end": null,
          "aa_length": 1806,
          "cds_start": 4885,
          "cds_end": null,
          "cds_length": 5421,
          "cdna_start": 5037,
          "cdna_end": null,
          "cdna_length": 7321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4885_4887delAAA",
          "hgvs_p": "p.Lys1629del",
          "transcript": "ENST00000692716.1",
          "protein_id": "ENSP00000509545.1",
          "transcript_support_level": null,
          "aa_start": 1629,
          "aa_end": null,
          "aa_length": 1806,
          "cds_start": 4885,
          "cds_end": null,
          "cds_length": 5421,
          "cdna_start": 5039,
          "cdna_end": null,
          "cdna_length": 9215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4621_4623delAAA",
          "hgvs_p": "p.Lys1541del",
          "transcript": "ENST00000688344.1",
          "protein_id": "ENSP00000509987.1",
          "transcript_support_level": null,
          "aa_start": 1541,
          "aa_end": null,
          "aa_length": 1718,
          "cds_start": 4621,
          "cds_end": null,
          "cds_length": 5157,
          "cdna_start": 4623,
          "cdna_end": null,
          "cdna_length": 6763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "conservative_inframe_deletion"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.3718_3720delAAA",
          "hgvs_p": "p.Lys1240del",
          "transcript": "ENST00000689597.1",
          "protein_id": "ENSP00000510781.1",
          "transcript_support_level": null,
          "aa_start": 1240,
          "aa_end": null,
          "aa_length": 1312,
          "cds_start": 3718,
          "cds_end": null,
          "cds_length": 3939,
          "cdna_start": 3720,
          "cdna_end": null,
          "cdna_length": 4133,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.1498_1500delAAA",
          "hgvs_p": null,
          "transcript": "ENST00000524961.6",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": 3559,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.1550_1552delAAA",
          "hgvs_p": null,
          "transcript": "ENST00000532095.2",
          "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,
          "cdna_end": null,
          "cdna_length": 1866,
          "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": 38,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.*1322_*1324delAAA",
          "hgvs_p": null,
          "transcript": "ENST00000676324.2",
          "protein_id": "ENSP00000502578.1",
          "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": 7085,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.*707_*709delAAA",
          "hgvs_p": null,
          "transcript": "ENST00000689342.1",
          "protein_id": "ENSP00000510508.1",
          "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": 3239,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.2185_2187delAAA",
          "hgvs_p": null,
          "transcript": "ENST00000689356.1",
          "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": 4194,
          "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"
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          "canonical": false,
          "protein_coding": false,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
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        {
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          "exon_rank": null,
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          "exon_count": 2,
          "intron_rank": 1,
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        },
        {
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          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SBF2-AS1",
          "gene_hgnc_id": 27438,
          "hgvs_c": "n.281+7080_281+7082delTTT",
          "hgvs_p": null,
          "transcript": "ENST00000731161.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 551,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "SBF2-AS1",
          "gene_hgnc_id": 27438,
          "hgvs_c": "n.212-20193_212-20191delTTT",
          "hgvs_p": null,
          "transcript": "NR_036485.1",
          "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,
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          "cdna_length": 2708,
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          "feature": null
        },
        {
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          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LOC105369149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.100-3214_100-3212delTTT",
          "hgvs_p": null,
          "transcript": "NR_188521.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
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          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 475,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SBF2",
      "gene_hgnc_id": 2135,
      "dbsnp": "rs750958357",
      "frequency_reference_population": 0.00044358152,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 716,
      "gnomad_exomes_af": 0.000424129,
      "gnomad_genomes_af": 0.000630269,
      "gnomad_exomes_ac": 620,
      "gnomad_genomes_ac": 96,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 5.722,
      "phylop100way_prediction": "Uncertain_significance",
      "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": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM4_Supporting,BS1_Supporting",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 1,
          "pathogenic_score": 1,
          "criteria": [
            "PM4_Supporting",
            "BS1_Supporting"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000256190.13",
          "gene_symbol": "SBF2",
          "hgnc_id": 2135,
          "effects": [
            "conservative_inframe_deletion"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.5014_5016delAAA",
          "hgvs_p": "p.Lys1672del"
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000534671.1",
          "gene_symbol": "SBF2-AS1",
          "hgnc_id": 27438,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.235+7080_235+7082delTTT",
          "hgvs_p": null
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "NR_188521.1",
          "gene_symbol": "LOC105369149",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.100-3214_100-3212delTTT",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Charcot-Marie-Tooth disease type 4,Charcot-Marie-Tooth disease type 4B2,Inborn genetic diseases,Peripheral neuropathy,not provided,not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:9",
      "phenotype_combined": "Peripheral neuropathy|Charcot-Marie-Tooth disease type 4B2|not specified|not provided|Charcot-Marie-Tooth disease type 4|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}