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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: 21-36937021-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=36937021&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "21",
"pos": 36937021,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000674895.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile",
"transcript": "NM_001352514.2",
"protein_id": "NP_001339443.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 873,
"cds_start": 865,
"cds_end": null,
"cds_length": 2622,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 8273,
"mane_select": "ENST00000674895.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile",
"transcript": "ENST00000674895.3",
"protein_id": "ENSP00000502087.2",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 873,
"cds_start": 865,
"cds_end": null,
"cds_length": 2622,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 8273,
"mane_select": "NM_001352514.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "ENST00000336648.8",
"protein_id": "ENSP00000338387.3",
"transcript_support_level": 1,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 895,
"cdna_end": null,
"cdna_length": 6010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "ENST00000399120.5",
"protein_id": "ENSP00000382071.1",
"transcript_support_level": 1,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 1655,
"cdna_end": null,
"cdna_length": 6466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_000411.8",
"protein_id": "NP_000402.3",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 870,
"cdna_end": null,
"cdna_length": 8247,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001242784.3",
"protein_id": "NP_001229713.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 1851,
"cdna_end": null,
"cdna_length": 9228,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001242785.2",
"protein_id": "NP_001229714.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 1027,
"cdna_end": null,
"cdna_length": 8405,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001352515.2",
"protein_id": "NP_001339444.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 724,
"cdna_end": null,
"cdna_length": 8101,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001352516.2",
"protein_id": "NP_001339445.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 927,
"cdna_end": null,
"cdna_length": 8304,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001352517.1",
"protein_id": "NP_001339446.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 881,
"cdna_end": null,
"cdna_length": 8259,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "NM_001352518.2",
"protein_id": "NP_001339447.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 740,
"cdna_end": null,
"cdna_length": 8117,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "ENST00000612277.4",
"protein_id": "ENSP00000479939.1",
"transcript_support_level": 5,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 997,
"cdna_end": null,
"cdna_length": 6112,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "ENST00000675307.1",
"protein_id": "ENSP00000501750.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 819,
"cdna_end": null,
"cdna_length": 4757,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.709G>A",
"hgvs_p": "p.Val237Ile",
"transcript": "XM_047440752.1",
"protein_id": "XP_047296708.1",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 821,
"cds_start": 709,
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"cdna_start": 4197,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile",
"transcript": "XM_047440753.1",
"protein_id": "XP_047296709.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 751,
"cds_start": 865,
"cds_end": null,
"cds_length": 2256,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 2527,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "XM_047440754.1",
"protein_id": "XP_047296710.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 726,
"cds_start": 424,
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"cdna_start": 555,
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"cdna_length": 7933,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.253G>A",
"hgvs_p": "p.Val85Ile",
"transcript": "XM_024452065.2",
"protein_id": "XP_024307833.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 669,
"cds_start": 253,
"cds_end": null,
"cds_length": 2010,
"cdna_start": 561,
"cdna_end": null,
"cdna_length": 7939,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile",
"transcript": "XM_011529540.3",
"protein_id": "XP_011527842.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 636,
"cds_start": 865,
"cds_end": null,
"cds_length": 1911,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 5245,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile",
"transcript": "XM_047440755.1",
"protein_id": "XP_047296711.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 550,
"cds_start": 865,
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"cdna_start": 896,
"cdna_end": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Val142Ile",
"transcript": "XM_047440756.1",
"protein_id": "XP_047296712.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 489,
"cds_start": 424,
"cds_end": null,
"cds_length": 1470,
"cdna_start": 724,
"cdna_end": null,
"cdna_length": 5073,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "n.424G>A",
"hgvs_p": null,
"transcript": "ENST00000675057.1",
"protein_id": "ENSP00000501832.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4903,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "n.724G>A",
"hgvs_p": null,
"transcript": "NR_148020.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8326,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "n.881G>A",
"hgvs_p": null,
"transcript": "NR_148021.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8484,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.*147G>A",
"hgvs_p": null,
"transcript": "ENST00000448340.5",
"protein_id": "ENSP00000392923.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 91,
"cds_start": -4,
"cds_end": null,
"cds_length": 277,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 780,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"hgvs_c": "c.*193G>A",
"hgvs_p": null,
"transcript": "ENST00000427746.1",
"protein_id": "ENSP00000396443.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 76,
"cds_start": -4,
"cds_end": null,
"cds_length": 231,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 666,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "HLCS",
"gene_hgnc_id": 4976,
"dbsnp": "rs149291867",
"frequency_reference_population": 0.00082955934,
"hom_count_reference_population": 11,
"allele_count_reference_population": 1339,
"gnomad_exomes_af": 0.000831803,
"gnomad_genomes_af": 0.000808009,
"gnomad_exomes_ac": 1216,
"gnomad_genomes_ac": 123,
"gnomad_exomes_homalt": 10,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.003075122833251953,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.165,
"revel_prediction": "Benign",
"alphamissense_score": 0.0708,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.35,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.913,
"phylop100way_prediction": "Benign",
"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": -13,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BS1,BS2",
"acmg_by_gene": [
{
"score": -13,
"benign_score": 13,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000674895.3",
"gene_symbol": "HLCS",
"hgnc_id": 4976,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.865G>A",
"hgvs_p": "p.Val289Ile"
}
],
"clinvar_disease": "HLCS-related disorder,Holocarboxylase synthetase deficiency,Inborn genetic diseases,not provided,not specified",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:3 LB:2 B:2",
"phenotype_combined": "Holocarboxylase synthetase deficiency|not specified|HLCS-related disorder|not provided|Inborn genetic diseases",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}