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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: 19-48053037-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=48053037&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 48053037,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001159322.2",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1540A>G",
"hgvs_p": "p.Asn514Asp",
"transcript": "NM_003706.3",
"protein_id": "NP_003697.2",
"transcript_support_level": null,
"aa_start": 514,
"aa_end": null,
"aa_length": 541,
"cds_start": 1540,
"cds_end": null,
"cds_length": 1626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000599921.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003706.3"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1540A>G",
"hgvs_p": "p.Asn514Asp",
"transcript": "ENST00000599921.6",
"protein_id": "ENSP00000469473.1",
"transcript_support_level": 1,
"aa_start": 514,
"aa_end": null,
"aa_length": 541,
"cds_start": 1540,
"cds_end": null,
"cds_length": 1626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003706.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000599921.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "n.293A>G",
"hgvs_p": null,
"transcript": "ENST00000594790.1",
"protein_id": null,
"transcript_support_level": 1,
"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": "retained_intron",
"feature": "ENST00000594790.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1597A>G",
"hgvs_p": "p.Asn533Asp",
"transcript": "ENST00000887096.1",
"protein_id": "ENSP00000557155.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 560,
"cds_start": 1597,
"cds_end": null,
"cds_length": 1683,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887096.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1573A>G",
"hgvs_p": "p.Asn525Asp",
"transcript": "ENST00000887093.1",
"protein_id": "ENSP00000557152.1",
"transcript_support_level": null,
"aa_start": 525,
"aa_end": null,
"aa_length": 552,
"cds_start": 1573,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887093.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1570A>G",
"hgvs_p": "p.Asn524Asp",
"transcript": "NM_001159322.2",
"protein_id": "NP_001152794.1",
"transcript_support_level": null,
"aa_start": 524,
"aa_end": null,
"aa_length": 551,
"cds_start": 1570,
"cds_end": null,
"cds_length": 1656,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001159322.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1570A>G",
"hgvs_p": "p.Asn524Asp",
"transcript": "ENST00000599111.5",
"protein_id": "ENSP00000472546.1",
"transcript_support_level": 2,
"aa_start": 524,
"aa_end": null,
"aa_length": 551,
"cds_start": 1570,
"cds_end": null,
"cds_length": 1656,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000599111.5"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1519A>G",
"hgvs_p": "p.Asn507Asp",
"transcript": "ENST00000951724.1",
"protein_id": "ENSP00000621783.1",
"transcript_support_level": null,
"aa_start": 507,
"aa_end": null,
"aa_length": 534,
"cds_start": 1519,
"cds_end": null,
"cds_length": 1605,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951724.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1540A>G",
"hgvs_p": "p.Asn514Asp",
"transcript": "NM_001159323.2",
"protein_id": "NP_001152795.1",
"transcript_support_level": null,
"aa_start": 514,
"aa_end": null,
"aa_length": 527,
"cds_start": 1540,
"cds_end": null,
"cds_length": 1584,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001159323.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1540A>G",
"hgvs_p": "p.Asn514Asp",
"transcript": "ENST00000354276.7",
"protein_id": "ENSP00000346228.2",
"transcript_support_level": 2,
"aa_start": 514,
"aa_end": null,
"aa_length": 527,
"cds_start": 1540,
"cds_end": null,
"cds_length": 1584,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000354276.7"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1486A>G",
"hgvs_p": "p.Asn496Asp",
"transcript": "ENST00000887089.1",
"protein_id": "ENSP00000557148.1",
"transcript_support_level": null,
"aa_start": 496,
"aa_end": null,
"aa_length": 523,
"cds_start": 1486,
"cds_end": null,
"cds_length": 1572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887089.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1486A>G",
"hgvs_p": "p.Asn496Asp",
"transcript": "ENST00000887091.1",
"protein_id": "ENSP00000557150.1",
"transcript_support_level": null,
"aa_start": 496,
"aa_end": null,
"aa_length": 523,
"cds_start": 1486,
"cds_end": null,
"cds_length": 1572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887091.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1459A>G",
"hgvs_p": "p.Asn487Asp",
"transcript": "ENST00000887090.1",
"protein_id": "ENSP00000557149.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 514,
"cds_start": 1459,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887090.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1459A>G",
"hgvs_p": "p.Asn487Asp",
"transcript": "ENST00000951723.1",
"protein_id": "ENSP00000621782.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 514,
"cds_start": 1459,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951723.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1459A>G",
"hgvs_p": "p.Asn487Asp",
"transcript": "ENST00000951725.1",
"protein_id": "ENSP00000621784.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 514,
"cds_start": 1459,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951725.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1444A>G",
"hgvs_p": "p.Asn482Asp",
"transcript": "ENST00000951720.1",
"protein_id": "ENSP00000621779.1",
"transcript_support_level": null,
"aa_start": 482,
"aa_end": null,
"aa_length": 509,
"cds_start": 1444,
"cds_end": null,
"cds_length": 1530,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951720.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1432A>G",
"hgvs_p": "p.Asn478Asp",
"transcript": "ENST00000951719.1",
"protein_id": "ENSP00000621778.1",
"transcript_support_level": null,
"aa_start": 478,
"aa_end": null,
"aa_length": 505,
"cds_start": 1432,
"cds_end": null,
"cds_length": 1518,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951719.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1405A>G",
"hgvs_p": "p.Asn469Asp",
"transcript": "ENST00000887097.1",
"protein_id": "ENSP00000557156.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 496,
"cds_start": 1405,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887097.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1405A>G",
"hgvs_p": "p.Asn469Asp",
"transcript": "ENST00000951726.1",
"protein_id": "ENSP00000621785.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 496,
"cds_start": 1405,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951726.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1399A>G",
"hgvs_p": "p.Asn467Asp",
"transcript": "ENST00000887092.1",
"protein_id": "ENSP00000557151.1",
"transcript_support_level": null,
"aa_start": 467,
"aa_end": null,
"aa_length": 494,
"cds_start": 1399,
"cds_end": null,
"cds_length": 1485,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000887092.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1378A>G",
"hgvs_p": "p.Asn460Asp",
"transcript": "ENST00000951718.1",
"protein_id": "ENSP00000621777.1",
"transcript_support_level": null,
"aa_start": 460,
"aa_end": null,
"aa_length": 487,
"cds_start": 1378,
"cds_end": null,
"cds_length": 1464,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951718.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"hgvs_c": "c.1351A>G",
"hgvs_p": "p.Asn451Asp",
"transcript": "ENST00000951722.1",
"protein_id": "ENSP00000621781.1",
"transcript_support_level": null,
"aa_start": 451,
"aa_end": null,
"aa_length": 478,
"cds_start": 1351,
"cds_end": null,
"cds_length": 1437,
"cdna_start": null,
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},
{
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],
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},
{
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"protein_coding": true,
"strand": false,
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],
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"gene_symbol": "PLA2G4C",
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},
{
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"protein_coding": true,
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],
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"biotype": "protein_coding",
"feature": "ENST00000887095.1"
},
{
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"protein_coding": true,
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"consequences": [
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],
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"gene_symbol": "PLA2G4C",
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"hgvs_c": "c.1486A>G",
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"transcript": "XM_011527431.4",
"protein_id": "XP_011525733.1",
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"feature": "XM_011527431.4"
},
{
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"consequences": [
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],
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"gene_symbol": "PLA2G4C",
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"hgvs_c": "c.1003A>G",
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"transcript": "XM_047439585.1",
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"biotype": "protein_coding",
"feature": "XM_047439585.1"
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
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"exon_count": 6,
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"gene_symbol": "PLA2G4C",
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"hgvs_c": "n.1250A>G",
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"transcript": "ENST00000596510.5",
"protein_id": null,
"transcript_support_level": 2,
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"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000596510.5"
}
],
"gene_symbol": "PLA2G4C",
"gene_hgnc_id": 9037,
"dbsnp": "rs765830693",
"frequency_reference_population": 0.0000061589753,
"hom_count_reference_population": 0,
"allele_count_reference_population": 9,
"gnomad_exomes_af": 0.00000615898,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 9,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3808930516242981,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.129,
"revel_prediction": "Benign",
"alphamissense_score": 0.8561,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.63,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.225,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001159322.2",
"gene_symbol": "PLA2G4C",
"hgnc_id": 9037,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1570A>G",
"hgvs_p": "p.Asn524Asp"
}
],
"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
}