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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: 19-4839404-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=4839404&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 4839404,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_005817.5",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "NM_005817.5",
          "protein_id": "NP_005808.3",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000221957.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_005817.5"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000221957.9",
          "protein_id": "ENSP00000221957.3",
          "transcript_support_level": 1,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_005817.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000221957.9"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1090C>G",
          "hgvs_p": "p.Gln364Glu",
          "transcript": "ENST00000585479.5",
          "protein_id": "ENSP00000465596.1",
          "transcript_support_level": 1,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 433,
          "cds_start": 1090,
          "cds_end": null,
          "cds_length": 1302,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000585479.5"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000884464.1",
          "protein_id": "ENSP00000554523.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884464.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000884466.1",
          "protein_id": "ENSP00000554525.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884466.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000884467.1",
          "protein_id": "ENSP00000554526.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884467.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000928988.1",
          "protein_id": "ENSP00000599047.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000928988.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000928989.1",
          "protein_id": "ENSP00000599048.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000928989.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000958157.1",
          "protein_id": "ENSP00000628216.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000958157.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000958159.1",
          "protein_id": "ENSP00000628218.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000958159.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000958160.1",
          "protein_id": "ENSP00000628219.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000958160.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu",
          "transcript": "ENST00000958162.1",
          "protein_id": "ENSP00000628221.1",
          "transcript_support_level": null,
          "aa_start": 365,
          "aa_end": null,
          "aa_length": 434,
          "cds_start": 1093,
          "cds_end": null,
          "cds_length": 1305,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000958162.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1090C>G",
          "hgvs_p": "p.Gln364Glu",
          "transcript": "NM_001164189.2",
          "protein_id": "NP_001157661.1",
          "transcript_support_level": null,
          "aa_start": 364,
          "aa_end": null,
          "aa_length": 433,
          "cds_start": 1090,
          "cds_end": null,
          "cds_length": 1302,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001164189.2"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1084C>G",
          "hgvs_p": "p.Gln362Glu",
          "transcript": "ENST00000884463.1",
          "protein_id": "ENSP00000554522.1",
          "transcript_support_level": null,
          "aa_start": 362,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1084,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884463.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1081C>G",
          "hgvs_p": "p.Gln361Glu",
          "transcript": "ENST00000884460.1",
          "protein_id": "ENSP00000554519.1",
          "transcript_support_level": null,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 430,
          "cds_start": 1081,
          "cds_end": null,
          "cds_length": 1293,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884460.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1057C>G",
          "hgvs_p": "p.Gln353Glu",
          "transcript": "NM_001164194.2",
          "protein_id": "NP_001157666.1",
          "transcript_support_level": null,
          "aa_start": 353,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 1057,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001164194.2"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1057C>G",
          "hgvs_p": "p.Gln353Glu",
          "transcript": "ENST00000592528.5",
          "protein_id": "ENSP00000467803.1",
          "transcript_support_level": 2,
          "aa_start": 353,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 1057,
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          "cds_length": 1269,
          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000592528.5"
        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.1057C>G",
          "hgvs_p": "p.Gln353Glu",
          "transcript": "ENST00000958163.1",
          "protein_id": "ENSP00000628222.1",
          "transcript_support_level": null,
          "aa_start": 353,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 1057,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000958163.1"
        },
        {
          "aa_ref": "Q",
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          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.967C>G",
          "hgvs_p": "p.Gln323Glu",
          "transcript": "ENST00000884461.1",
          "protein_id": "ENSP00000554520.1",
          "transcript_support_level": null,
          "aa_start": 323,
          "aa_end": null,
          "aa_length": 392,
          "cds_start": 967,
          "cds_end": null,
          "cds_length": 1179,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000884461.1"
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.964C>G",
          "hgvs_p": "p.Gln322Glu",
          "transcript": "ENST00000884465.1",
          "protein_id": "ENSP00000554524.1",
          "transcript_support_level": null,
          "aa_start": 322,
          "aa_end": null,
          "aa_length": 391,
          "cds_start": 964,
          "cds_end": null,
          "cds_length": 1176,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        {
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        {
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          "gene_symbol": "PLIN3",
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          "protein_id": "ENSP00000628215.1",
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          "biotype": "protein_coding",
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        },
        {
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          "strand": false,
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            "missense_variant"
          ],
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          "exon_count": 5,
          "intron_rank": null,
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          "gene_symbol": "PLIN3",
          "gene_hgnc_id": 16893,
          "hgvs_c": "c.664C>G",
          "hgvs_p": "p.Gln222Glu",
          "transcript": "ENST00000589163.5",
          "protein_id": "ENSP00000468476.1",
          "transcript_support_level": 3,
          "aa_start": 222,
          "aa_end": null,
          "aa_length": 291,
          "cds_start": 664,
          "cds_end": null,
          "cds_length": 876,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000589163.5"
        }
      ],
      "gene_symbol": "PLIN3",
      "gene_hgnc_id": 16893,
      "dbsnp": null,
      "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": 0.1798323392868042,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.095,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0789,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.65,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.889,
      "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": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_005817.5",
          "gene_symbol": "PLIN3",
          "hgnc_id": 16893,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1093C>G",
          "hgvs_p": "p.Gln365Glu"
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}