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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: 6-107154674-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=107154674&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 107154674,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_020381.4",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1145C>T",
"hgvs_p": "p.Ser382Leu",
"transcript": "NM_020381.4",
"protein_id": "NP_065114.3",
"transcript_support_level": null,
"aa_start": 382,
"aa_end": null,
"aa_length": 399,
"cds_start": 1145,
"cds_end": null,
"cds_length": 1200,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000369037.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_020381.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1145C>T",
"hgvs_p": "p.Ser382Leu",
"transcript": "ENST00000369037.9",
"protein_id": "ENSP00000358033.4",
"transcript_support_level": 1,
"aa_start": 382,
"aa_end": null,
"aa_length": 399,
"cds_start": 1145,
"cds_end": null,
"cds_length": 1200,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_020381.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000369037.9"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1343C>T",
"hgvs_p": "p.Ser448Leu",
"transcript": "ENST00000900080.1",
"protein_id": "ENSP00000570139.1",
"transcript_support_level": null,
"aa_start": 448,
"aa_end": null,
"aa_length": 465,
"cds_start": 1343,
"cds_end": null,
"cds_length": 1398,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900080.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1208C>T",
"hgvs_p": "p.Ser403Leu",
"transcript": "ENST00000962908.1",
"protein_id": "ENSP00000632967.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 420,
"cds_start": 1208,
"cds_end": null,
"cds_length": 1263,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000962908.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1073C>T",
"hgvs_p": "p.Ser358Leu",
"transcript": "ENST00000900085.1",
"protein_id": "ENSP00000570144.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 375,
"cds_start": 1073,
"cds_end": null,
"cds_length": 1128,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900085.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1013C>T",
"hgvs_p": "p.Ser338Leu",
"transcript": "ENST00000900079.1",
"protein_id": "ENSP00000570138.1",
"transcript_support_level": null,
"aa_start": 338,
"aa_end": null,
"aa_length": 355,
"cds_start": 1013,
"cds_end": null,
"cds_length": 1068,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900079.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1010C>T",
"hgvs_p": "p.Ser337Leu",
"transcript": "ENST00000900083.1",
"protein_id": "ENSP00000570142.1",
"transcript_support_level": null,
"aa_start": 337,
"aa_end": null,
"aa_length": 354,
"cds_start": 1010,
"cds_end": null,
"cds_length": 1065,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900083.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.971C>T",
"hgvs_p": "p.Ser324Leu",
"transcript": "ENST00000900082.1",
"protein_id": "ENSP00000570141.1",
"transcript_support_level": null,
"aa_start": 324,
"aa_end": null,
"aa_length": 341,
"cds_start": 971,
"cds_end": null,
"cds_length": 1026,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900082.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.878C>T",
"hgvs_p": "p.Ser293Leu",
"transcript": "ENST00000934234.1",
"protein_id": "ENSP00000604293.1",
"transcript_support_level": null,
"aa_start": 293,
"aa_end": null,
"aa_length": 310,
"cds_start": 878,
"cds_end": null,
"cds_length": 933,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000934234.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.839C>T",
"hgvs_p": "p.Ser280Leu",
"transcript": "ENST00000900081.1",
"protein_id": "ENSP00000570140.1",
"transcript_support_level": null,
"aa_start": 280,
"aa_end": null,
"aa_length": 297,
"cds_start": 839,
"cds_end": null,
"cds_length": 894,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900081.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.836C>T",
"hgvs_p": "p.Ser279Leu",
"transcript": "ENST00000900084.1",
"protein_id": "ENSP00000570143.1",
"transcript_support_level": null,
"aa_start": 279,
"aa_end": null,
"aa_length": 296,
"cds_start": 836,
"cds_end": null,
"cds_length": 891,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900084.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.704C>T",
"hgvs_p": "p.Ser235Leu",
"transcript": "ENST00000900086.1",
"protein_id": "ENSP00000570145.1",
"transcript_support_level": null,
"aa_start": 235,
"aa_end": null,
"aa_length": 252,
"cds_start": 704,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900086.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1343C>T",
"hgvs_p": "p.Ser448Leu",
"transcript": "XM_011535956.4",
"protein_id": "XP_011534258.1",
"transcript_support_level": null,
"aa_start": 448,
"aa_end": null,
"aa_length": 465,
"cds_start": 1343,
"cds_end": null,
"cds_length": 1398,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535956.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1211C>T",
"hgvs_p": "p.Ser404Leu",
"transcript": "XM_011535957.4",
"protein_id": "XP_011534259.1",
"transcript_support_level": null,
"aa_start": 404,
"aa_end": null,
"aa_length": 421,
"cds_start": 1211,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535957.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1208C>T",
"hgvs_p": "p.Ser403Leu",
"transcript": "XM_011535958.4",
"protein_id": "XP_011534260.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 420,
"cds_start": 1208,
"cds_end": null,
"cds_length": 1263,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535958.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1037C>T",
"hgvs_p": "p.Ser346Leu",
"transcript": "XM_047419096.1",
"protein_id": "XP_047275052.1",
"transcript_support_level": null,
"aa_start": 346,
"aa_end": null,
"aa_length": 363,
"cds_start": 1037,
"cds_end": null,
"cds_length": 1092,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419096.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1013C>T",
"hgvs_p": "p.Ser338Leu",
"transcript": "XM_011535959.4",
"protein_id": "XP_011534261.1",
"transcript_support_level": null,
"aa_start": 338,
"aa_end": null,
"aa_length": 355,
"cds_start": 1013,
"cds_end": null,
"cds_length": 1068,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535959.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.1010C>T",
"hgvs_p": "p.Ser337Leu",
"transcript": "XM_047419097.1",
"protein_id": "XP_047275053.1",
"transcript_support_level": null,
"aa_start": 337,
"aa_end": null,
"aa_length": 354,
"cds_start": 1010,
"cds_end": null,
"cds_length": 1065,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419097.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.935C>T",
"hgvs_p": "p.Ser312Leu",
"transcript": "XM_011535960.4",
"protein_id": "XP_011534262.1",
"transcript_support_level": null,
"aa_start": 312,
"aa_end": null,
"aa_length": 329,
"cds_start": 935,
"cds_end": null,
"cds_length": 990,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535960.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.887C>T",
"hgvs_p": "p.Ser296Leu",
"transcript": "XM_047419098.1",
"protein_id": "XP_047275054.1",
"transcript_support_level": null,
"aa_start": 296,
"aa_end": null,
"aa_length": 313,
"cds_start": 887,
"cds_end": null,
"cds_length": 942,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419098.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.878C>T",
"hgvs_p": "p.Ser293Leu",
"transcript": "XM_047419099.1",
"protein_id": "XP_047275055.1",
"transcript_support_level": null,
"aa_start": 293,
"aa_end": null,
"aa_length": 310,
"cds_start": 878,
"cds_end": null,
"cds_length": 933,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419099.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.839C>T",
"hgvs_p": "p.Ser280Leu",
"transcript": "XM_011535961.4",
"protein_id": "XP_011534263.1",
"transcript_support_level": null,
"aa_start": 280,
"aa_end": null,
"aa_length": 297,
"cds_start": 839,
"cds_end": null,
"cds_length": 894,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535961.4"
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.803C>T",
"hgvs_p": "p.Ser268Leu",
"transcript": "XM_047419100.1",
"protein_id": "XP_047275056.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 285,
"cds_start": 803,
"cds_end": null,
"cds_length": 858,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419100.1"
},
{
"aa_ref": "S",
"aa_alt": "L",
"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": "PDSS2",
"gene_hgnc_id": 23041,
"hgvs_c": "c.704C>T",
"hgvs_p": "p.Ser235Leu",
"transcript": "XM_047419101.1",
"protein_id": "XP_047275057.1",
"transcript_support_level": null,
"aa_start": 235,
"aa_end": null,
"aa_length": 252,
"cds_start": 704,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047419101.1"
}
],
"gene_symbol": "PDSS2",
"gene_hgnc_id": 23041,
"dbsnp": "rs118203956",
"frequency_reference_population": 0.000021685415,
"hom_count_reference_population": 0,
"allele_count_reference_population": 35,
"gnomad_exomes_af": 0.0000218907,
"gnomad_genomes_af": 0.0000197138,
"gnomad_exomes_ac": 32,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8626240491867065,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.737,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.5801,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.3,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 8.174,
"phylop100way_prediction": "Pathogenic",
"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": "Uncertain_significance",
"acmg_criteria": "PM2,PP3_Moderate,PP5",
"acmg_by_gene": [
{
"score": 5,
"benign_score": 0,
"pathogenic_score": 5,
"criteria": [
"PM2",
"PP3_Moderate",
"PP5"
],
"verdict": "Uncertain_significance",
"transcript": "NM_020381.4",
"gene_symbol": "PDSS2",
"hgnc_id": 23041,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1145C>T",
"hgvs_p": "p.Ser382Leu"
}
],
"clinvar_disease": " 3, primary,Coenzyme Q10 deficiency,Nephrotic syndrome,not provided,not specified",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "LP:1 US:2 O:1",
"phenotype_combined": "Coenzyme Q10 deficiency, primary, 3|Nephrotic syndrome|not specified|not provided",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}