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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: 16-67199999-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=67199999&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 67199999,
"ref": "C",
"alt": "T",
"effect": "missense_variant,splice_region_variant",
"transcript": "NM_024712.5",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "NM_024712.5",
"protein_id": "NP_078988.3",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 720,
"cds_start": 241,
"cds_end": null,
"cds_length": 2163,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000393997.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_024712.5"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000393997.8",
"protein_id": "ENSP00000377566.3",
"transcript_support_level": 2,
"aa_start": 81,
"aa_end": null,
"aa_length": 720,
"cds_start": 241,
"cds_end": null,
"cds_length": 2163,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_024712.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393997.8"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.400C>T",
"hgvs_p": "p.Pro134Ser",
"transcript": "ENST00000652269.1",
"protein_id": "ENSP00000498602.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 773,
"cds_start": 400,
"cds_end": null,
"cds_length": 2322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000652269.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.289C>T",
"hgvs_p": "p.Pro97Ser",
"transcript": "ENST00000874722.1",
"protein_id": "ENSP00000544781.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 734,
"cds_start": 289,
"cds_end": null,
"cds_length": 2205,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874722.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000921646.1",
"protein_id": "ENSP00000591705.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 725,
"cds_start": 241,
"cds_end": null,
"cds_length": 2178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921646.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874723.1",
"protein_id": "ENSP00000544782.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 719,
"cds_start": 241,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874723.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874718.1",
"protein_id": "ENSP00000544777.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 718,
"cds_start": 241,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874718.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874720.1",
"protein_id": "ENSP00000544779.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 717,
"cds_start": 241,
"cds_end": null,
"cds_length": 2154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874720.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000921645.1",
"protein_id": "ENSP00000591704.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 712,
"cds_start": 241,
"cds_end": null,
"cds_length": 2139,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921645.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000966544.1",
"protein_id": "ENSP00000636603.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 712,
"cds_start": 241,
"cds_end": null,
"cds_length": 2139,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966544.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874719.1",
"protein_id": "ENSP00000544778.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 709,
"cds_start": 241,
"cds_end": null,
"cds_length": 2130,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874719.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874721.1",
"protein_id": "ENSP00000544780.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 699,
"cds_start": 241,
"cds_end": null,
"cds_length": 2100,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874721.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874717.1",
"protein_id": "ENSP00000544776.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 694,
"cds_start": 241,
"cds_end": null,
"cds_length": 2085,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874717.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000874716.1",
"protein_id": "ENSP00000544775.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 685,
"cds_start": 241,
"cds_end": null,
"cds_length": 2058,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874716.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000921647.1",
"protein_id": "ENSP00000591706.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 636,
"cds_start": 241,
"cds_end": null,
"cds_length": 1911,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921647.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser",
"transcript": "ENST00000966543.1",
"protein_id": "ENSP00000636602.1",
"transcript_support_level": null,
"aa_start": 81,
"aa_end": null,
"aa_length": 630,
"cds_start": 241,
"cds_end": null,
"cds_length": 1893,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966543.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.-99C>T",
"hgvs_p": null,
"transcript": "ENST00000477898.5",
"protein_id": "ENSP00000458539.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 607,
"cds_start": null,
"cds_end": null,
"cds_length": 1824,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000477898.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.-99C>T",
"hgvs_p": null,
"transcript": "ENST00000477898.5",
"protein_id": "ENSP00000458539.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 607,
"cds_start": null,
"cds_end": null,
"cds_length": 1824,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000477898.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "c.193-193C>T",
"hgvs_p": null,
"transcript": "ENST00000360833.6",
"protein_id": "ENSP00000354077.2",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": null,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360833.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "n.*101C>T",
"hgvs_p": null,
"transcript": "ENST00000571587.6",
"protein_id": "ENSP00000461166.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000571587.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "n.49C>T",
"hgvs_p": null,
"transcript": "ENST00000571638.1",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000571638.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "n.437C>T",
"hgvs_p": null,
"transcript": "XR_007064916.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_007064916.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"hgvs_c": "n.*101C>T",
"hgvs_p": null,
"transcript": "ENST00000571587.6",
"protein_id": "ENSP00000461166.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000571587.6"
}
],
"gene_symbol": "ELMO3",
"gene_hgnc_id": 17289,
"dbsnp": "rs200097822",
"frequency_reference_population": 0.000035944337,
"hom_count_reference_population": 0,
"allele_count_reference_population": 58,
"gnomad_exomes_af": 0.000019844,
"gnomad_genomes_af": 0.000190531,
"gnomad_exomes_ac": 29,
"gnomad_genomes_ac": 29,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.6708297729492188,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.863707423210144,
"splice_prediction_selected": "Benign",
"splice_source_selected": "dbscSNV1_ADA",
"revel_score": 0.561,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.5474,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.09,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 2.458,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": 0.863707430287298,
"dbscsnv_ada_prediction": "Benign",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "NM_024712.5",
"gene_symbol": "ELMO3",
"hgnc_id": 17289,
"effects": [
"missense_variant",
"splice_region_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.241C>T",
"hgvs_p": "p.Pro81Ser"
}
],
"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
}