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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: 22-26457915-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=26457915&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 26457915,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "NM_001349900.2",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "NM_022081.6",
"protein_id": "NP_071364.4",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000398145.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_022081.6"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000398145.7",
"protein_id": "ENSP00000381213.2",
"transcript_support_level": 1,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_022081.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000398145.7"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1884C>T",
"hgvs_p": "p.Val628Val",
"transcript": "ENST00000402105.7",
"protein_id": "ENSP00000384185.3",
"transcript_support_level": 1,
"aa_start": 628,
"aa_end": null,
"aa_length": 703,
"cds_start": 1884,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402105.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "n.*1417C>T",
"hgvs_p": null,
"transcript": "ENST00000439453.5",
"protein_id": "ENSP00000406764.1",
"transcript_support_level": 1,
"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": "nonsense_mediated_decay",
"feature": "ENST00000439453.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "n.4758C>T",
"hgvs_p": null,
"transcript": "ENST00000466781.5",
"protein_id": null,
"transcript_support_level": 1,
"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": "retained_intron",
"feature": "ENST00000466781.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "n.*1417C>T",
"hgvs_p": null,
"transcript": "ENST00000439453.5",
"protein_id": "ENSP00000406764.1",
"transcript_support_level": 1,
"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": "nonsense_mediated_decay",
"feature": "ENST00000439453.5"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val",
"transcript": "NM_001349900.2",
"protein_id": "NP_001336829.1",
"transcript_support_level": null,
"aa_start": 651,
"aa_end": null,
"aa_length": 726,
"cds_start": 1953,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349900.2"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val",
"transcript": "NM_001349901.1",
"protein_id": "NP_001336830.1",
"transcript_support_level": null,
"aa_start": 651,
"aa_end": null,
"aa_length": 726,
"cds_start": 1953,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349901.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val",
"transcript": "ENST00000422379.3",
"protein_id": "ENSP00000415081.3",
"transcript_support_level": 5,
"aa_start": 651,
"aa_end": null,
"aa_length": 726,
"cds_start": 1953,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000422379.3"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val",
"transcript": "ENST00000885020.1",
"protein_id": "ENSP00000555079.1",
"transcript_support_level": null,
"aa_start": 651,
"aa_end": null,
"aa_length": 726,
"cds_start": 1953,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885020.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val",
"transcript": "ENST00000885021.1",
"protein_id": "ENSP00000555080.1",
"transcript_support_level": null,
"aa_start": 651,
"aa_end": null,
"aa_length": 726,
"cds_start": 1953,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885021.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "NM_001349896.1",
"protein_id": "NP_001336825.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349896.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "NM_001349898.2",
"protein_id": "NP_001336827.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349898.2"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "NM_001349899.2",
"protein_id": "NP_001336828.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349899.2"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000336873.9",
"protein_id": "ENSP00000338457.5",
"transcript_support_level": 5,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000336873.9"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000473782.2",
"protein_id": "ENSP00000514223.1",
"transcript_support_level": 2,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000473782.2"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000885018.1",
"protein_id": "ENSP00000555077.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885018.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000885019.1",
"protein_id": "ENSP00000555078.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885019.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000940090.1",
"protein_id": "ENSP00000610149.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000940090.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "ENST00000940092.1",
"protein_id": "ENSP00000610151.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 708,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000940092.1"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1884C>T",
"hgvs_p": "p.Val628Val",
"transcript": "NM_152841.2",
"protein_id": "NP_690054.1",
"transcript_support_level": null,
"aa_start": 628,
"aa_end": null,
"aa_length": 703,
"cds_start": 1884,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_152841.2"
},
{
"aa_ref": "V",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "c.1899C>T",
"hgvs_p": "p.Val633Val",
"transcript": "NM_001410832.1",
"protein_id": "NP_001397761.1",
"transcript_support_level": null,
"aa_start": 633,
"aa_end": null,
"aa_length": 680,
"cds_start": 1899,
"cds_end": null,
"cds_length": 2043,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001410832.1"
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"canonical": false,
"protein_coding": false,
"strand": false,
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"exon_count": 8,
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{
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],
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"exon_count": 13,
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"gene_symbol": "HPS4",
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"hgvs_c": "n.*1058-4511C>T",
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"transcript": "ENST00000699249.1",
"protein_id": "ENSP00000514236.1",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000699249.1"
},
{
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"protein_coding": false,
"strand": false,
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"intron_variant"
],
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"exon_count": 13,
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"gene_symbol": "HPS4",
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"hgvs_c": "n.2291-4511C>T",
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"transcript": "XR_001755364.2",
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"biotype": "pseudogene",
"feature": "XR_001755364.2"
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{
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"strand": false,
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"intron_variant"
],
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"exon_count": 14,
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"gene_symbol": "HPS4",
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"hgvs_c": "n.2356-4511C>T",
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"biotype": "pseudogene",
"feature": "XR_007067988.1"
},
{
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"intron_variant"
],
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"exon_count": 13,
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"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"hgvs_c": "n.2302-4511C>T",
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"transcript": "XR_007067989.1",
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"biotype": "pseudogene",
"feature": "XR_007067989.1"
}
],
"gene_symbol": "HPS4",
"gene_hgnc_id": 15844,
"dbsnp": "rs35993959",
"frequency_reference_population": 0.0026521075,
"hom_count_reference_population": 92,
"allele_count_reference_population": 4281,
"gnomad_exomes_af": 0.0014393,
"gnomad_genomes_af": 0.0142883,
"gnomad_exomes_ac": 2104,
"gnomad_genomes_ac": 2177,
"gnomad_exomes_homalt": 39,
"gnomad_genomes_homalt": 53,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.3799999952316284,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.38,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.628,
"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": -19,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BS1,BS2",
"acmg_by_gene": [
{
"score": -19,
"benign_score": 19,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Very_Strong",
"BP7",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001349900.2",
"gene_symbol": "HPS4",
"hgnc_id": 15844,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1953C>T",
"hgvs_p": "p.Val651Val"
}
],
"clinvar_disease": "Hermansky-Pudlak syndrome,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2 B:4",
"phenotype_combined": "not specified|Hermansky-Pudlak syndrome|not provided",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}