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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: 3-69203748-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=69203748&ref=C&alt=T&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": "FRMD4B",
"hgnc_id": 24886,
"hgvs_c": "c.877-4974G>A",
"hgvs_p": null,
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -12,
"transcript": "NM_015123.3",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_score": -12,
"allele_count_reference_population": 13032,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.86,
"chr": "3",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.8600000143051147,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1034,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6283,
"cdna_start": null,
"cds_end": null,
"cds_length": 3105,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 23,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_015123.3",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.877-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000398540.8",
"protein_coding": true,
"protein_id": "NP_055938.2",
"strand": false,
"transcript": "NM_015123.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1034,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 6283,
"cdna_start": null,
"cds_end": null,
"cds_length": 3105,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 23,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000398540.8",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.877-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_015123.3",
"protein_coding": true,
"protein_id": "ENSP00000381549.3",
"strand": false,
"transcript": "ENST00000398540.8",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1014,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4793,
"cdna_start": null,
"cds_end": null,
"cds_length": 3045,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 23,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000863518.1",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.877-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000533577.1",
"strand": false,
"transcript": "ENST00000863518.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1063,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6375,
"cdna_start": null,
"cds_end": null,
"cds_length": 3192,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 24,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017005989.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.877-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016861478.1",
"strand": false,
"transcript": "XM_017005989.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1018,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6258,
"cdna_start": null,
"cds_end": null,
"cds_length": 3057,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 24,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017005990.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.742-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016861479.1",
"strand": false,
"transcript": "XM_017005990.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1009,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6365,
"cdna_start": null,
"cds_end": null,
"cds_length": 3030,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017005991.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.715-4974G>A",
"hgvs_p": null,
"intron_rank": 12,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016861480.1",
"strand": false,
"transcript": "XM_017005991.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1009,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6172,
"cdna_start": null,
"cds_end": null,
"cds_length": 3030,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 24,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017005992.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.715-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016861481.1",
"strand": false,
"transcript": "XM_017005992.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1009,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6623,
"cdna_start": null,
"cds_end": null,
"cds_length": 3030,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047447767.1",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.715-4974G>A",
"hgvs_p": null,
"intron_rank": 12,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047303723.1",
"strand": false,
"transcript": "XM_047447767.1",
"transcript_support_level": null
},
{
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8047,
"cdna_start": null,
"cds_end": null,
"cds_length": 3030,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 24,
"exon_rank": null,
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"feature": "XM_047447768.1",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.715-4974G>A",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047303724.1",
"strand": false,
"transcript": "XM_047447768.1",
"transcript_support_level": null
},
{
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"biotype": "protein_coding",
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"cdna_end": null,
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"cdna_start": null,
"cds_end": null,
"cds_length": 2970,
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"consequences": [
"intron_variant"
],
"exon_count": 23,
"exon_rank": null,
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"feature": "XM_005264722.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.742-4974G>A",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_005264779.1",
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"transcript": "XM_005264722.2",
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},
{
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"consequences": [
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],
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"feature": "XM_017005993.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_016861482.1",
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},
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_016861483.1",
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},
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"protein_coding": true,
"protein_id": "XP_047303725.1",
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},
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"consequences": [
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],
"exon_count": 23,
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"feature": "XM_047447770.1",
"gene_hgnc_id": 24886,
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"hgvs_c": "c.715-4974G>A",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_047303726.1",
"strand": false,
"transcript": "XM_047447770.1",
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},
{
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],
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"feature": "XM_047447771.1",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_047303727.1",
"strand": false,
"transcript": "XM_047447771.1",
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},
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"consequences": [
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],
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"feature": "XM_017005995.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.142-4974G>A",
"hgvs_p": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "XP_016861484.1",
"strand": false,
"transcript": "XM_017005995.2",
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},
{
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"consequences": [
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],
"exon_count": 18,
"exon_rank": null,
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"feature": "XM_047447772.1",
"gene_hgnc_id": 24886,
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},
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],
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"feature": "ENST00000470070.6",
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"transcript": "ENST00000470070.6",
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},
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],
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"feature": "ENST00000483668.5",
"gene_hgnc_id": 24886,
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"transcript": "ENST00000483668.5",
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},
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"consequences": [
"intron_variant"
],
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"exon_rank": null,
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"feature": "ENST00000487751.1",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "n.502-4974G>A",
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"mane_plus": null,
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"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000487751.1",
"transcript_support_level": 4
},
{
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"biotype": "protein_coding",
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"cdna_start": null,
"cds_end": null,
"cds_length": 2325,
"cds_start": null,
"consequences": [
"upstream_gene_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017005996.2",
"gene_hgnc_id": 24886,
"gene_symbol": "FRMD4B",
"hgvs_c": "c.-2928G>A",
"hgvs_p": null,
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016861485.1",
"strand": true,
"transcript": "XM_017005996.2",
"transcript_support_level": null
},
{
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