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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: 14-65076553-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=65076553&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 65076553,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_002382.5",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.406G>T",
"hgvs_p": "p.Gly136Trp",
"transcript": "NM_002382.5",
"protein_id": "NP_002373.3",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 160,
"cds_start": 406,
"cds_end": null,
"cds_length": 483,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000358664.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002382.5"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.406G>T",
"hgvs_p": "p.Gly136Trp",
"transcript": "ENST00000358664.9",
"protein_id": "ENSP00000351490.4",
"transcript_support_level": 1,
"aa_start": 136,
"aa_end": null,
"aa_length": 160,
"cds_start": 406,
"cds_end": null,
"cds_length": 483,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002382.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000358664.9"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.379G>T",
"hgvs_p": "p.Gly127Trp",
"transcript": "ENST00000358402.8",
"protein_id": "ENSP00000351175.4",
"transcript_support_level": 1,
"aa_start": 127,
"aa_end": null,
"aa_length": 151,
"cds_start": 379,
"cds_end": null,
"cds_length": 456,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000358402.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.*1250G>T",
"hgvs_p": null,
"transcript": "ENST00000284165.10",
"protein_id": "ENSP00000284165.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 134,
"cds_start": null,
"cds_end": null,
"cds_length": 405,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000284165.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "n.*179G>T",
"hgvs_p": null,
"transcript": "ENST00000394606.6",
"protein_id": "ENSP00000378104.2",
"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": "nonsense_mediated_decay",
"feature": "ENST00000394606.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "n.*195G>T",
"hgvs_p": null,
"transcript": "ENST00000553928.5",
"protein_id": "ENSP00000451907.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000553928.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "n.*179G>T",
"hgvs_p": null,
"transcript": "ENST00000394606.6",
"protein_id": "ENSP00000378104.2",
"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": "nonsense_mediated_decay",
"feature": "ENST00000394606.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "n.*195G>T",
"hgvs_p": null,
"transcript": "ENST00000553928.5",
"protein_id": "ENSP00000451907.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000553928.5"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.460G>T",
"hgvs_p": "p.Gly154Trp",
"transcript": "ENST00000937808.1",
"protein_id": "ENSP00000607867.1",
"transcript_support_level": null,
"aa_start": 154,
"aa_end": null,
"aa_length": 178,
"cds_start": 460,
"cds_end": null,
"cds_length": 537,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000937808.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.406G>T",
"hgvs_p": "p.Gly136Trp",
"transcript": "NM_001407094.1",
"protein_id": "NP_001394023.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 160,
"cds_start": 406,
"cds_end": null,
"cds_length": 483,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407094.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.379G>T",
"hgvs_p": "p.Gly127Trp",
"transcript": "NM_001407095.1",
"protein_id": "NP_001394024.1",
"transcript_support_level": null,
"aa_start": 127,
"aa_end": null,
"aa_length": 151,
"cds_start": 379,
"cds_end": null,
"cds_length": 456,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407095.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.379G>T",
"hgvs_p": "p.Gly127Trp",
"transcript": "NM_145112.3",
"protein_id": "NP_660087.1",
"transcript_support_level": null,
"aa_start": 127,
"aa_end": null,
"aa_length": 151,
"cds_start": 379,
"cds_end": null,
"cds_length": 456,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_145112.3"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.298G>T",
"hgvs_p": "p.Gly100Trp",
"transcript": "NM_001407098.1",
"protein_id": "NP_001394027.1",
"transcript_support_level": null,
"aa_start": 100,
"aa_end": null,
"aa_length": 124,
"cds_start": 298,
"cds_end": null,
"cds_length": 375,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407098.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.298G>T",
"hgvs_p": "p.Gly100Trp",
"transcript": "ENST00000555419.5",
"protein_id": "ENSP00000452405.1",
"transcript_support_level": 5,
"aa_start": 100,
"aa_end": null,
"aa_length": 124,
"cds_start": 298,
"cds_end": null,
"cds_length": 375,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000555419.5"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.238G>T",
"hgvs_p": "p.Gly80Trp",
"transcript": "ENST00000937807.1",
"protein_id": "ENSP00000607866.1",
"transcript_support_level": null,
"aa_start": 80,
"aa_end": null,
"aa_length": 104,
"cds_start": 238,
"cds_end": null,
"cds_length": 315,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000937807.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.217G>T",
"hgvs_p": "p.Gly73Trp",
"transcript": "NM_001320415.2",
"protein_id": "NP_001307344.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 97,
"cds_start": 217,
"cds_end": null,
"cds_length": 294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001320415.2"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.217G>T",
"hgvs_p": "p.Gly73Trp",
"transcript": "NM_001407105.1",
"protein_id": "NP_001394034.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 97,
"cds_start": 217,
"cds_end": null,
"cds_length": 294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407105.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.217G>T",
"hgvs_p": "p.Gly73Trp",
"transcript": "NM_001407106.1",
"protein_id": "NP_001394035.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 97,
"cds_start": 217,
"cds_end": null,
"cds_length": 294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407106.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.217G>T",
"hgvs_p": "p.Gly73Trp",
"transcript": "NM_001407107.1",
"protein_id": "NP_001394036.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 97,
"cds_start": 217,
"cds_end": null,
"cds_length": 294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407107.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.217G>T",
"hgvs_p": "p.Gly73Trp",
"transcript": "ENST00000557277.5",
"protein_id": "ENSP00000450955.1",
"transcript_support_level": 3,
"aa_start": 73,
"aa_end": null,
"aa_length": 97,
"cds_start": 217,
"cds_end": null,
"cds_length": 294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000557277.5"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.205G>T",
"hgvs_p": "p.Gly69Trp",
"transcript": "NM_001407111.1",
"protein_id": "NP_001394040.1",
"transcript_support_level": null,
"aa_start": 69,
"aa_end": null,
"aa_length": 93,
"cds_start": 205,
"cds_end": null,
"cds_length": 282,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407111.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "c.205G>T",
"hgvs_p": "p.Gly69Trp",
"transcript": "NM_001407112.1",
"protein_id": "NP_001394041.1",
"transcript_support_level": null,
"aa_start": 69,
"aa_end": null,
"aa_length": 93,
"cds_start": 205,
"cds_end": null,
"cds_length": 282,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407112.1"
},
{
"aa_ref": "G",
"aa_alt": "W",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
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{
"aa_ref": null,
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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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAX",
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"hgvs_c": "n.453G>T",
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"transcript": "NR_176282.1",
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"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,
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"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_176282.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 2,
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"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"hgvs_c": "n.145-6184G>T",
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"transcript": "ENST00000651648.1",
"protein_id": "ENSP00000498863.1",
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"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": "ENST00000651648.1"
}
],
"gene_symbol": "MAX",
"gene_hgnc_id": 6913,
"dbsnp": "rs140490467",
"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": 0.3530954122543335,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.569,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.9352,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.21,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 5.7,
"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": 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_002382.5",
"gene_symbol": "MAX",
"hgnc_id": 6913,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.406G>T",
"hgvs_p": "p.Gly136Trp"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}