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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: 6-135013462-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=135013462&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 12,
"criteria": [
"BP4_Strong",
"BA1"
],
"effects": [
"intron_variant"
],
"gene_symbol": "HBS1L",
"hgnc_id": 4834,
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -12,
"transcript": "NM_006620.4",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_score": -12,
"allele_count_reference_population": 80486,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -1.05,
"chr": "6",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Benign",
"computational_score_selected": -1.0499999523162842,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": null,
"aa_end": null,
"aa_length": 684,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7087,
"cdna_start": null,
"cds_end": null,
"cds_length": 2055,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_006620.4",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000367837.10",
"protein_coding": true,
"protein_id": "NP_006611.1",
"strand": false,
"transcript": "NM_006620.4",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 684,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 7087,
"cdna_start": null,
"cds_end": null,
"cds_length": 2055,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000367837.10",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_006620.4",
"protein_coding": true,
"protein_id": "ENSP00000356811.5",
"strand": false,
"transcript": "ENST00000367837.10",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 520,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2618,
"cdna_start": null,
"cds_end": null,
"cds_length": 1563,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000527578.5",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.-62-10620T>C",
"hgvs_p": null,
"intron_rank": 1,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000436256.1",
"strand": false,
"transcript": "ENST00000527578.5",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 690,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2854,
"cdna_start": null,
"cds_end": null,
"cds_length": 2073,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 19,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000949311.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619370.1",
"strand": false,
"transcript": "ENST00000949311.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 683,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2840,
"cdna_start": null,
"cds_end": null,
"cds_length": 2052,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000881131.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000551190.1",
"strand": false,
"transcript": "ENST00000881131.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 682,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2438,
"cdna_start": null,
"cds_end": null,
"cds_length": 2049,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000919570.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000589629.1",
"strand": false,
"transcript": "ENST00000919570.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 661,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2764,
"cdna_start": null,
"cds_end": null,
"cds_length": 1986,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000949313.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619372.1",
"strand": false,
"transcript": "ENST00000949313.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 642,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6961,
"cdna_start": null,
"cds_end": null,
"cds_length": 1929,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001145158.2",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.305-10620T>C",
"hgvs_p": null,
"intron_rank": 3,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001138630.1",
"strand": false,
"transcript": "NM_001145158.2",
"transcript_support_level": null
},
{
"aa_alt": null,
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"aa_length": 642,
"aa_ref": null,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2703,
"cdna_start": null,
"cds_end": null,
"cds_length": 1929,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000367826.6",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.305-10620T>C",
"hgvs_p": null,
"intron_rank": 3,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000356800.2",
"strand": false,
"transcript": "ENST00000367826.6",
"transcript_support_level": 2
},
{
"aa_alt": null,
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"aa_length": 635,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2680,
"cdna_start": null,
"cds_end": null,
"cds_length": 1908,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000949314.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619373.1",
"strand": false,
"transcript": "ENST00000949314.1",
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},
{
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"cdna_start": null,
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"cds_length": 1860,
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"consequences": [
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],
"exon_count": 17,
"exon_rank": null,
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"feature": "ENST00000415177.6",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.236-10620T>C",
"hgvs_p": null,
"intron_rank": 3,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000389826.2",
"strand": false,
"transcript": "ENST00000415177.6",
"transcript_support_level": 5
},
{
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"biotype": "protein_coding",
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"consequences": [
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],
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"feature": "ENST00000949312.1",
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"gene_symbol": "HBS1L",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000619371.1",
"strand": false,
"transcript": "ENST00000949312.1",
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},
{
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],
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"feature": "ENST00000533274.5",
"gene_hgnc_id": 4834,
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"hgvs_c": "c.41-10620T>C",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000434533.1",
"strand": false,
"transcript": "ENST00000533274.5",
"transcript_support_level": 2
},
{
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
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"cds_end": null,
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"cds_start": null,
"consequences": [
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],
"exon_count": 19,
"exon_rank": null,
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"feature": "NM_001363686.2",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.-208-2703T>C",
"hgvs_p": null,
"intron_rank": 4,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "NP_001350615.1",
"strand": false,
"transcript": "NM_001363686.2",
"transcript_support_level": null
},
{
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],
"exon_count": 6,
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"feature": "ENST00000529641.5",
"gene_hgnc_id": 4834,
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"hgvs_c": "c.-62-10620T>C",
"hgvs_p": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000436620.1",
"strand": false,
"transcript": "ENST00000529641.5",
"transcript_support_level": 5
},
{
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"biotype": "protein_coding",
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"cdna_end": null,
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"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 6,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000314674.7",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.647-10620T>C",
"hgvs_p": null,
"intron_rank": 5,
"intron_rank_end": null,
"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000323566.3",
"strand": false,
"transcript": "ENST00000314674.7",
"transcript_support_level": 5
},
{
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 544,
"cdna_start": null,
"cds_end": null,
"cds_length": 503,
"cds_start": null,
"consequences": [
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],
"exon_count": 5,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000529882.5",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.476-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000433030.1",
"strand": false,
"transcript": "ENST00000529882.5",
"transcript_support_level": 4
},
{
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"consequences": [
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],
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"feature": "ENST00000527507.1",
"gene_hgnc_id": 4834,
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"mane_plus": null,
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"protein_id": "ENSP00000432092.1",
"strand": false,
"transcript": "ENST00000527507.1",
"transcript_support_level": 4
},
{
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"consequences": [
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],
"exon_count": 4,
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"feature": "ENST00000524715.5",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.365-10620T>C",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000434855.1",
"strand": false,
"transcript": "ENST00000524715.5",
"transcript_support_level": 4
},
{
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"biotype": "protein_coding",
"canonical": false,
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"cdna_start": null,
"cds_end": null,
"cds_length": 1809,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 16,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047418093.1",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "c.431-10620T>C",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047274049.1",
"strand": false,
"transcript": "XM_047418093.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1600,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000526100.5",
"gene_hgnc_id": 4834,
"gene_symbol": "HBS1L",
"hgvs_c": "n.188-16041T>C",
"hgvs_p": null,
"intron_rank": 2,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000433161.1",
"strand": false,
"transcript": "ENST00000526100.5",
"transcript_support_level": 2
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs1014021",
"effect": "intron_variant",
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}
]
}