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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: 11-68537848-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=68537848&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 68537848,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001352354.2",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001164161.2",
"protein_id": "NP_001157633.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000393800.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001164161.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000393800.7",
"protein_id": "ENSP00000377389.2",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001164161.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393800.7"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000393801.7",
"protein_id": "ENSP00000377390.3",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 879,
"cds_start": 184,
"cds_end": null,
"cds_length": 2640,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393801.7"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000524904.5",
"protein_id": "ENSP00000433058.1",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 867,
"cds_start": 184,
"cds_end": null,
"cds_length": 2604,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000524904.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000524845.5",
"protein_id": "ENSP00000431415.1",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 844,
"cds_start": 184,
"cds_end": null,
"cds_length": 2535,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000524845.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000265636.9",
"protein_id": "ENSP00000265636.4",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 793,
"cds_start": 184,
"cds_end": null,
"cds_length": 2382,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000265636.9"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000529710.5",
"protein_id": "ENSP00000437329.1",
"transcript_support_level": 1,
"aa_start": 62,
"aa_end": null,
"aa_length": 791,
"cds_start": 184,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000529710.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000871875.1",
"protein_id": "ENSP00000541934.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 904,
"cds_start": 184,
"cds_end": null,
"cds_length": 2715,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871875.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352354.2",
"protein_id": "NP_001339283.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 889,
"cds_start": 184,
"cds_end": null,
"cds_length": 2670,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352354.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352356.2",
"protein_id": "NP_001339285.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 889,
"cds_start": 184,
"cds_end": null,
"cds_length": 2670,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352356.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000929898.1",
"protein_id": "ENSP00000599957.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 880,
"cds_start": 184,
"cds_end": null,
"cds_length": 2643,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929898.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001164160.2",
"protein_id": "NP_001157632.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 879,
"cds_start": 184,
"cds_end": null,
"cds_length": 2640,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001164160.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352364.2",
"protein_id": "NP_001339293.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 879,
"cds_start": 184,
"cds_end": null,
"cds_length": 2640,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352364.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352379.2",
"protein_id": "NP_001339308.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 879,
"cds_start": 184,
"cds_end": null,
"cds_length": 2640,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352379.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000953359.1",
"protein_id": "ENSP00000623418.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 879,
"cds_start": 184,
"cds_end": null,
"cds_length": 2640,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953359.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352368.2",
"protein_id": "NP_001339297.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352368.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352372.2",
"protein_id": "NP_001339301.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352372.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352375.2",
"protein_id": "NP_001339304.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352375.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "NM_001352377.2",
"protein_id": "NP_001339306.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001352377.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000871853.1",
"protein_id": "ENSP00000541912.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871853.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000871854.1",
"protein_id": "ENSP00000541913.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
"cds_start": 184,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871854.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu",
"transcript": "ENST00000871863.1",
"protein_id": "ENSP00000541922.1",
"transcript_support_level": null,
"aa_start": 62,
"aa_end": null,
"aa_length": 873,
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"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "c.*159A>T",
"hgvs_p": null,
"transcript": "ENST00000528635.5",
"protein_id": "ENSP00000436789.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 7,
"cds_start": null,
"cds_end": null,
"cds_length": 25,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000528635.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"hgvs_c": "n.*179A>T",
"hgvs_p": null,
"transcript": "ENST00000530427.5",
"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": "ENST00000530427.5"
}
],
"gene_symbol": "PPP6R3",
"gene_hgnc_id": 1173,
"dbsnp": "rs140917558",
"frequency_reference_population": 0.0000024786618,
"hom_count_reference_population": 0,
"allele_count_reference_population": 4,
"gnomad_exomes_af": 0.00000136844,
"gnomad_genomes_af": 0.0000131358,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3236241340637207,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.249,
"revel_prediction": "Benign",
"alphamissense_score": 0.3154,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.21,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 7.416,
"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_001352354.2",
"gene_symbol": "PPP6R3",
"hgnc_id": 1173,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.184A>T",
"hgvs_p": "p.Ile62Leu"
}
],
"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
}