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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: 2-119245717-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=119245717&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 119245717,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_182915.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "NM_182915.3",
"protein_id": "NP_878919.2",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 699,
"cdna_end": null,
"cdna_length": 4259,
"mane_select": "ENST00000393110.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_182915.3"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000393110.7",
"protein_id": "ENSP00000376822.2",
"transcript_support_level": 1,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 699,
"cdna_end": null,
"cdna_length": 4259,
"mane_select": "NM_182915.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393110.7"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "ENST00000393106.6",
"protein_id": "ENSP00000376818.2",
"transcript_support_level": 1,
"aa_start": 74,
"aa_end": null,
"aa_length": 488,
"cds_start": 221,
"cds_end": null,
"cds_length": 1467,
"cdna_start": 355,
"cdna_end": null,
"cdna_length": 3915,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393106.6"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "ENST00000393107.2",
"protein_id": "ENSP00000376819.2",
"transcript_support_level": 1,
"aa_start": 74,
"aa_end": null,
"aa_length": 488,
"cds_start": 221,
"cds_end": null,
"cds_length": 1467,
"cdna_start": 265,
"cdna_end": null,
"cdna_length": 1871,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393107.2"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "ENST00000409811.5",
"protein_id": "ENSP00000386510.1",
"transcript_support_level": 1,
"aa_start": 74,
"aa_end": null,
"aa_length": 457,
"cds_start": 221,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 265,
"cdna_end": null,
"cdna_length": 2103,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409811.5"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869398.1",
"protein_id": "ENSP00000539457.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 843,
"cdna_end": null,
"cdna_length": 4403,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869398.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869399.1",
"protein_id": "ENSP00000539458.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 889,
"cdna_end": null,
"cdna_length": 4446,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869399.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869400.1",
"protein_id": "ENSP00000539459.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 895,
"cdna_end": null,
"cdna_length": 4455,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869400.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869401.1",
"protein_id": "ENSP00000539460.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 704,
"cdna_end": null,
"cdna_length": 4261,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869401.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869402.1",
"protein_id": "ENSP00000539461.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 1090,
"cdna_end": null,
"cdna_length": 4647,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869402.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869403.1",
"protein_id": "ENSP00000539462.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 763,
"cdna_end": null,
"cdna_length": 4320,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869403.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869404.1",
"protein_id": "ENSP00000539463.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 758,
"cdna_end": null,
"cdna_length": 4318,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869404.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869405.1",
"protein_id": "ENSP00000539464.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 596,
"cdna_end": null,
"cdna_length": 4156,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869405.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869406.1",
"protein_id": "ENSP00000539465.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 970,
"cdna_end": null,
"cdna_length": 2455,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869406.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "ENST00000869407.1",
"protein_id": "ENSP00000539466.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 2189,
"cdna_end": null,
"cdna_length": 5749,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000869407.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "NM_001008410.2",
"protein_id": "NP_001008410.1",
"transcript_support_level": null,
"aa_start": 74,
"aa_end": null,
"aa_length": 488,
"cds_start": 221,
"cds_end": null,
"cds_length": 1467,
"cdna_start": 284,
"cdna_end": null,
"cdna_length": 3844,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001008410.2"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "NM_018234.3",
"protein_id": "NP_060704.2",
"transcript_support_level": null,
"aa_start": 74,
"aa_end": null,
"aa_length": 488,
"cds_start": 221,
"cds_end": null,
"cds_length": 1467,
"cdna_start": 352,
"cdna_end": null,
"cdna_length": 3912,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_018234.3"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "NM_138637.3",
"protein_id": "NP_619543.2",
"transcript_support_level": null,
"aa_start": 74,
"aa_end": null,
"aa_length": 457,
"cds_start": 221,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 284,
"cdna_end": null,
"cdna_length": 4076,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_138637.3"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala",
"transcript": "XM_047444895.1",
"protein_id": "XP_047300851.1",
"transcript_support_level": null,
"aa_start": 84,
"aa_end": null,
"aa_length": 498,
"cds_start": 251,
"cds_end": null,
"cds_length": 1497,
"cdna_start": 579,
"cdna_end": null,
"cdna_length": 4139,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047444895.1"
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"hgvs_c": "c.221T>C",
"hgvs_p": "p.Val74Ala",
"transcript": "XM_011511403.2",
"protein_id": "XP_011509705.1",
"transcript_support_level": null,
"aa_start": 74,
"aa_end": null,
"aa_length": 488,
"cds_start": 221,
"cds_end": null,
"cds_length": 1467,
"cdna_start": 767,
"cdna_end": null,
"cdna_length": 4327,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011511403.2"
},
{
"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": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3-AS1",
"gene_hgnc_id": 41053,
"hgvs_c": "n.1923A>G",
"hgvs_p": null,
"transcript": "ENST00000454260.1",
"protein_id": null,
"transcript_support_level": 2,
"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": 3218,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000454260.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3-AS1",
"gene_hgnc_id": 41053,
"hgvs_c": "n.1325A>G",
"hgvs_p": null,
"transcript": "ENST00000654197.1",
"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": 2588,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000654197.1"
},
{
"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": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STEAP3-AS1",
"gene_hgnc_id": 41053,
"hgvs_c": "n.1923A>G",
"hgvs_p": null,
"transcript": "NR_046721.1",
"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": 3218,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_046721.1"
}
],
"gene_symbol": "STEAP3",
"gene_hgnc_id": 24592,
"dbsnp": "rs1677396787",
"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": 0.6658402681350708,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.214,
"revel_prediction": "Benign",
"alphamissense_score": 0.4624,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.34,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 8.014,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.01,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_182915.3",
"gene_symbol": "STEAP3",
"hgnc_id": 24592,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.251T>C",
"hgvs_p": "p.Val84Ala"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000454260.1",
"gene_symbol": "STEAP3-AS1",
"hgnc_id": 41053,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.1923A>G",
"hgvs_p": null
}
],
"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
}