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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: X-139596585-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=139596585&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 139596585,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "ENST00000519895.6",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2469C>T",
"hgvs_p": "p.Asp823Asp",
"transcript": "NM_001171876.2",
"protein_id": "NP_001165347.1",
"transcript_support_level": null,
"aa_start": 823,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2469,
"cds_end": null,
"cds_length": 3006,
"cdna_start": 2575,
"cdna_end": null,
"cdna_length": 3813,
"mane_select": "ENST00000519895.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2469C>T",
"hgvs_p": "p.Asp823Asp",
"transcript": "ENST00000519895.6",
"protein_id": "ENSP00000430276.1",
"transcript_support_level": 2,
"aa_start": 823,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2469,
"cds_end": null,
"cds_length": 3006,
"cdna_start": 2575,
"cdna_end": null,
"cdna_length": 3813,
"mane_select": "NM_001171876.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2289C>T",
"hgvs_p": "p.Asp763Asp",
"transcript": "ENST00000338585.6",
"protein_id": "ENSP00000342204.6",
"transcript_support_level": 1,
"aa_start": 763,
"aa_end": null,
"aa_length": 941,
"cds_start": 2289,
"cds_end": null,
"cds_length": 2826,
"cdna_start": 2289,
"cdna_end": null,
"cdna_length": 2826,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2241C>T",
"hgvs_p": "p.Asp747Asp",
"transcript": "ENST00000370576.9",
"protein_id": "ENSP00000359608.4",
"transcript_support_level": 1,
"aa_start": 747,
"aa_end": null,
"aa_length": 925,
"cds_start": 2241,
"cds_end": null,
"cds_length": 2778,
"cdna_start": 2626,
"cdna_end": null,
"cdna_length": 3864,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2241C>T",
"hgvs_p": "p.Asp747Asp",
"transcript": "ENST00000370573.8",
"protein_id": "ENSP00000359605.4",
"transcript_support_level": 1,
"aa_start": 747,
"aa_end": null,
"aa_length": 860,
"cds_start": 2241,
"cds_end": null,
"cds_length": 2583,
"cdna_start": 2241,
"cdna_end": null,
"cdna_length": 2583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.1050C>T",
"hgvs_p": "p.Asp350Asp",
"transcript": "ENST00000446225.5",
"protein_id": "ENSP00000405848.1",
"transcript_support_level": 1,
"aa_start": 350,
"aa_end": null,
"aa_length": 528,
"cds_start": 1050,
"cds_end": null,
"cds_length": 1587,
"cdna_start": 1050,
"cdna_end": null,
"cdna_length": 1916,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.750C>T",
"hgvs_p": "p.Asp250Asp",
"transcript": "ENST00000437564.5",
"protein_id": "ENSP00000403271.1",
"transcript_support_level": 1,
"aa_start": 250,
"aa_end": null,
"aa_length": 428,
"cds_start": 750,
"cds_end": null,
"cds_length": 1287,
"cdna_start": 751,
"cdna_end": null,
"cdna_length": 1988,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2550C>T",
"hgvs_p": "p.Asp850Asp",
"transcript": "ENST00000520602.6",
"protein_id": "ENSP00000427745.2",
"transcript_support_level": 5,
"aa_start": 850,
"aa_end": null,
"aa_length": 1028,
"cds_start": 2550,
"cds_end": null,
"cds_length": 3087,
"cdna_start": 2707,
"cdna_end": null,
"cdna_length": 3945,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2421C>T",
"hgvs_p": "p.Asp807Asp",
"transcript": "NM_001099855.2",
"protein_id": "NP_001093325.1",
"transcript_support_level": null,
"aa_start": 807,
"aa_end": null,
"aa_length": 985,
"cds_start": 2421,
"cds_end": null,
"cds_length": 2958,
"cdna_start": 2527,
"cdna_end": null,
"cdna_length": 3765,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2421C>T",
"hgvs_p": "p.Asp807Asp",
"transcript": "ENST00000414978.5",
"protein_id": "ENSP00000397055.1",
"transcript_support_level": 5,
"aa_start": 807,
"aa_end": null,
"aa_length": 985,
"cds_start": 2421,
"cds_end": null,
"cds_length": 2958,
"cdna_start": 2576,
"cdna_end": null,
"cdna_length": 3813,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2289C>T",
"hgvs_p": "p.Asp763Asp",
"transcript": "NM_001171879.2",
"protein_id": "NP_001165350.1",
"transcript_support_level": null,
"aa_start": 763,
"aa_end": null,
"aa_length": 941,
"cds_start": 2289,
"cds_end": null,
"cds_length": 2826,
"cdna_start": 2674,
"cdna_end": null,
"cdna_length": 3912,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2241C>T",
"hgvs_p": "p.Asp747Asp",
"transcript": "NM_005369.6",
"protein_id": "NP_005360.3",
"transcript_support_level": null,
"aa_start": 747,
"aa_end": null,
"aa_length": 925,
"cds_start": 2241,
"cds_end": null,
"cds_length": 2778,
"cdna_start": 2626,
"cdna_end": null,
"cdna_length": 3864,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2241C>T",
"hgvs_p": "p.Asp747Asp",
"transcript": "NM_001171878.2",
"protein_id": "NP_001165349.1",
"transcript_support_level": null,
"aa_start": 747,
"aa_end": null,
"aa_length": 860,
"cds_start": 2241,
"cds_end": null,
"cds_length": 2583,
"cdna_start": 2626,
"cdna_end": null,
"cdna_length": 3641,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2124C>T",
"hgvs_p": "p.Asp708Asp",
"transcript": "NM_001171877.2",
"protein_id": "NP_001165348.1",
"transcript_support_level": null,
"aa_start": 708,
"aa_end": null,
"aa_length": 821,
"cds_start": 2124,
"cds_end": null,
"cds_length": 2466,
"cdna_start": 2509,
"cdna_end": null,
"cdna_length": 3524,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2124C>T",
"hgvs_p": "p.Asp708Asp",
"transcript": "ENST00000536274.5",
"protein_id": "ENSP00000438155.1",
"transcript_support_level": 2,
"aa_start": 708,
"aa_end": null,
"aa_length": 821,
"cds_start": 2124,
"cds_end": null,
"cds_length": 2466,
"cdna_start": 2447,
"cdna_end": null,
"cdna_length": 3461,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2598C>T",
"hgvs_p": "p.Asp866Asp",
"transcript": "XM_005262413.5",
"protein_id": "XP_005262470.1",
"transcript_support_level": null,
"aa_start": 866,
"aa_end": null,
"aa_length": 1044,
"cds_start": 2598,
"cds_end": null,
"cds_length": 3135,
"cdna_start": 2666,
"cdna_end": null,
"cdna_length": 3904,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2598C>T",
"hgvs_p": "p.Asp866Asp",
"transcript": "XM_017029529.2",
"protein_id": "XP_016885018.1",
"transcript_support_level": null,
"aa_start": 866,
"aa_end": null,
"aa_length": 1041,
"cds_start": 2598,
"cds_end": null,
"cds_length": 3126,
"cdna_start": 2666,
"cdna_end": null,
"cdna_length": 4172,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2469C>T",
"hgvs_p": "p.Asp823Asp",
"transcript": "XM_011531339.3",
"protein_id": "XP_011529641.1",
"transcript_support_level": null,
"aa_start": 823,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2469,
"cds_end": null,
"cds_length": 3006,
"cdna_start": 2725,
"cdna_end": null,
"cdna_length": 3963,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2469C>T",
"hgvs_p": "p.Asp823Asp",
"transcript": "XM_017029531.2",
"protein_id": "XP_016885020.1",
"transcript_support_level": null,
"aa_start": 823,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2469,
"cds_end": null,
"cds_length": 3006,
"cdna_start": 2531,
"cdna_end": null,
"cdna_length": 3769,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2598C>T",
"hgvs_p": "p.Asp866Asp",
"transcript": "XM_047442112.1",
"protein_id": "XP_047298068.1",
"transcript_support_level": null,
"aa_start": 866,
"aa_end": null,
"aa_length": 979,
"cds_start": 2598,
"cds_end": null,
"cds_length": 2940,
"cdna_start": 2666,
"cdna_end": null,
"cdna_length": 3681,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2550C>T",
"hgvs_p": "p.Asp850Asp",
"transcript": "XM_047442111.1",
"protein_id": "XP_047298067.1",
"transcript_support_level": null,
"aa_start": 850,
"aa_end": null,
"aa_length": 963,
"cds_start": 2550,
"cds_end": null,
"cds_length": 2892,
"cdna_start": 2551,
"cdna_end": null,
"cdna_length": 3566,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2289C>T",
"hgvs_p": "p.Asp763Asp",
"transcript": "XM_017029532.3",
"protein_id": "XP_016885021.1",
"transcript_support_level": null,
"aa_start": 763,
"aa_end": null,
"aa_length": 938,
"cds_start": 2289,
"cds_end": null,
"cds_length": 2817,
"cdna_start": 2674,
"cdna_end": null,
"cdna_length": 4180,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.2241C>T",
"hgvs_p": "p.Asp747Asp",
"transcript": "XM_047442113.1",
"protein_id": "XP_047298069.1",
"transcript_support_level": null,
"aa_start": 747,
"aa_end": null,
"aa_length": 922,
"cds_start": 2241,
"cds_end": null,
"cds_length": 2769,
"cdna_start": 2626,
"cdna_end": null,
"cdna_length": 4132,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"hgvs_c": "c.1263C>T",
"hgvs_p": "p.Asp421Asp",
"transcript": "XM_047442114.1",
"protein_id": "XP_047298070.1",
"transcript_support_level": null,
"aa_start": 421,
"aa_end": null,
"aa_length": 599,
"cds_start": 1263,
"cds_end": null,
"cds_length": 1800,
"cdna_start": 1466,
"cdna_end": null,
"cdna_length": 2704,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MCF2",
"gene_hgnc_id": 6940,
"dbsnp": "rs2235708",
"frequency_reference_population": 0.021330327,
"hom_count_reference_population": 8668,
"allele_count_reference_population": 25770,
"gnomad_exomes_af": 0.0193452,
"gnomad_genomes_af": 0.0408169,
"gnomad_exomes_ac": 21211,
"gnomad_genomes_ac": 4559,
"gnomad_exomes_homalt": 383,
"gnomad_genomes_homalt": 116,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.800000011920929,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.03999999910593033,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.8,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.153,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.04,
"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": -21,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
"acmg_by_gene": [
{
"score": -21,
"benign_score": 21,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000519895.6",
"gene_symbol": "MCF2",
"hgnc_id": 6940,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.2469C>T",
"hgvs_p": "p.Asp823Asp"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}