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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: 6-348266-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=348266&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 348266,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001286555.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Val143Ile",
"transcript": "NM_001286555.3",
"protein_id": "NP_001273484.1",
"transcript_support_level": null,
"aa_start": 143,
"aa_end": null,
"aa_length": 205,
"cds_start": 427,
"cds_end": null,
"cds_length": 618,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 3075,
"mane_select": "ENST00000419235.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001286555.3"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Val143Ile",
"transcript": "ENST00000419235.7",
"protein_id": "ENSP00000397459.2",
"transcript_support_level": 2,
"aa_start": 143,
"aa_end": null,
"aa_length": 205,
"cds_start": 427,
"cds_end": null,
"cds_length": 618,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 3075,
"mane_select": "NM_001286555.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000419235.7"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Val143Ile",
"transcript": "ENST00000344450.9",
"protein_id": "ENSP00000345281.5",
"transcript_support_level": 1,
"aa_start": 143,
"aa_end": null,
"aa_length": 184,
"cds_start": 427,
"cds_end": null,
"cds_length": 555,
"cdna_start": 870,
"cdna_end": null,
"cdna_length": 1485,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000344450.9"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Val143Ile",
"transcript": "NM_020185.6",
"protein_id": "NP_064570.1",
"transcript_support_level": null,
"aa_start": 143,
"aa_end": null,
"aa_length": 184,
"cds_start": 427,
"cds_end": null,
"cds_length": 555,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 1095,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_020185.6"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.118G>A",
"hgvs_p": "p.Val40Ile",
"transcript": "ENST00000603453.5",
"protein_id": "ENSP00000474646.1",
"transcript_support_level": 4,
"aa_start": 40,
"aa_end": null,
"aa_length": 102,
"cds_start": 118,
"cds_end": null,
"cds_length": 309,
"cdna_start": 610,
"cdna_end": null,
"cdna_length": 804,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000603453.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.118G>A",
"hgvs_p": "p.Val40Ile",
"transcript": "ENST00000604971.5",
"protein_id": "ENSP00000474505.1",
"transcript_support_level": 2,
"aa_start": 40,
"aa_end": null,
"aa_length": 102,
"cds_start": 118,
"cds_end": null,
"cds_length": 309,
"cdna_start": 1231,
"cdna_end": null,
"cdna_length": 3824,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000604971.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.118G>A",
"hgvs_p": "p.Val40Ile",
"transcript": "ENST00000605315.5",
"protein_id": "ENSP00000474827.1",
"transcript_support_level": 5,
"aa_start": 40,
"aa_end": null,
"aa_length": 102,
"cds_start": 118,
"cds_end": null,
"cds_length": 309,
"cdna_start": 525,
"cdna_end": null,
"cdna_length": 867,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000605315.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.118G>A",
"hgvs_p": "p.Val40Ile",
"transcript": "ENST00000605035.5",
"protein_id": "ENSP00000475061.1",
"transcript_support_level": 2,
"aa_start": 40,
"aa_end": null,
"aa_length": 46,
"cds_start": 118,
"cds_end": null,
"cds_length": 141,
"cdna_start": 440,
"cdna_end": null,
"cdna_length": 1231,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000605035.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.118G>A",
"hgvs_p": "p.Val40Ile",
"transcript": "ENST00000605863.5",
"protein_id": "ENSP00000474000.1",
"transcript_support_level": 4,
"aa_start": 40,
"aa_end": null,
"aa_length": 46,
"cds_start": 118,
"cds_end": null,
"cds_length": 141,
"cdna_start": 321,
"cdna_end": null,
"cdna_length": 551,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000605863.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.247G>A",
"hgvs_p": "p.Val83Ile",
"transcript": "XM_011514757.3",
"protein_id": "XP_011513059.1",
"transcript_support_level": null,
"aa_start": 83,
"aa_end": null,
"aa_length": 145,
"cds_start": 247,
"cds_end": null,
"cds_length": 438,
"cdna_start": 315,
"cdna_end": null,
"cdna_length": 2910,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514757.3"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.247G>A",
"hgvs_p": "p.Val83Ile",
"transcript": "XM_017011062.2",
"protein_id": "XP_016866551.1",
"transcript_support_level": null,
"aa_start": 83,
"aa_end": null,
"aa_length": 124,
"cds_start": 247,
"cds_end": null,
"cds_length": 375,
"cdna_start": 315,
"cdna_end": null,
"cdna_length": 930,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017011062.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.349G>A",
"hgvs_p": null,
"transcript": "ENST00000603005.5",
"protein_id": null,
"transcript_support_level": 3,
"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": 352,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000603005.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.*212G>A",
"hgvs_p": null,
"transcript": "ENST00000603726.5",
"protein_id": "ENSP00000474330.1",
"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": 587,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000603726.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.*212G>A",
"hgvs_p": null,
"transcript": "ENST00000603795.5",
"protein_id": "ENSP00000475106.1",
"transcript_support_level": 3,
"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": 1166,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000603795.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.388G>A",
"hgvs_p": null,
"transcript": "ENST00000604914.5",
"protein_id": null,
"transcript_support_level": 4,
"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": 536,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000604914.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.315G>A",
"hgvs_p": null,
"transcript": "ENST00000604988.1",
"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": 503,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000604988.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.430G>A",
"hgvs_p": null,
"transcript": "NR_104473.3",
"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": 3025,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_104473.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.397G>A",
"hgvs_p": null,
"transcript": "NR_104474.3",
"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": 2992,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_104474.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.313G>A",
"hgvs_p": null,
"transcript": "NR_104475.3",
"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": 2908,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_104475.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.*212G>A",
"hgvs_p": null,
"transcript": "ENST00000603726.5",
"protein_id": "ENSP00000474330.1",
"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": 587,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000603726.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.*212G>A",
"hgvs_p": null,
"transcript": "ENST00000603795.5",
"protein_id": "ENSP00000475106.1",
"transcript_support_level": 3,
"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": 1166,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000603795.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.*72G>A",
"hgvs_p": null,
"transcript": "ENST00000603296.5",
"protein_id": "ENSP00000474082.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 74,
"cds_start": null,
"cds_end": null,
"cds_length": 226,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 405,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000603296.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "c.*34G>A",
"hgvs_p": null,
"transcript": "ENST00000603881.5",
"protein_id": "ENSP00000474450.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 17,
"cds_start": null,
"cds_end": null,
"cds_length": 56,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 465,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000603881.5"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"hgvs_c": "n.*105G>A",
"hgvs_p": null,
"transcript": "ENST00000605391.5",
"protein_id": null,
"transcript_support_level": 4,
"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": 547,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000605391.5"
}
],
"gene_symbol": "DUSP22",
"gene_hgnc_id": 16077,
"dbsnp": "rs147464089",
"frequency_reference_population": 0.0013642827,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2201,
"gnomad_exomes_af": 0.00138199,
"gnomad_genomes_af": 0.00119452,
"gnomad_exomes_ac": 2019,
"gnomad_genomes_ac": 182,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0038633346557617188,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.227,
"revel_prediction": "Benign",
"alphamissense_score": 0.1128,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.41,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.743,
"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": -5,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong,BP6",
"acmg_by_gene": [
{
"score": -5,
"benign_score": 5,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6"
],
"verdict": "Likely_benign",
"transcript": "NM_001286555.3",
"gene_symbol": "DUSP22",
"hgnc_id": 16077,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Val143Ile"
}
],
"clinvar_disease": "DUSP22-related disorder",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "DUSP22-related disorder",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}