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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: 2-54977362-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=54977362&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 54977362,
"ref": "G",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000337526.11",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.3361-2598C>G",
"hgvs_p": null,
"transcript": "NM_020532.5",
"protein_id": "NP_065393.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1192,
"cds_start": -4,
"cds_end": null,
"cds_length": 3579,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4697,
"mane_select": "ENST00000337526.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.3361-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000337526.11",
"protein_id": "ENSP00000337838.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1192,
"cds_start": -4,
"cds_end": null,
"cds_length": 3579,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4697,
"mane_select": "NM_020532.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.2743-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000357376.7",
"protein_id": "ENSP00000349944.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
"cds_end": null,
"cds_length": 2961,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4110,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.2743-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000394611.6",
"protein_id": "ENSP00000378109.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
"cds_end": null,
"cds_length": 2961,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4161,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.2743-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000404909.5",
"protein_id": "ENSP00000385650.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
"cds_end": null,
"cds_length": 2961,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4102,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.2743-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000405240.5",
"protein_id": "ENSP00000384471.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.961-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000357732.8",
"protein_id": "ENSP00000350365.4",
"transcript_support_level": 1,
"aa_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.904-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000317610.11",
"protein_id": "ENSP00000322147.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 373,
"cds_start": -4,
"cds_end": null,
"cds_length": 1122,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2333,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"hgvs_c": "c.382-2598C>G",
"hgvs_p": null,
"transcript": "ENST00000394609.6",
"protein_id": "ENSP00000378107.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
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"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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},
{
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],
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"hgvs_c": "c.2743-2598C>G",
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"transcript": "NM_001321859.2",
"protein_id": "NP_001308788.1",
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},
{
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"consequences": [
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],
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"gene_symbol": "RTN4",
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{
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],
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],
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],
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],
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"feature": null
}
],
"gene_symbol": "RTN4",
"gene_hgnc_id": 14085,
"dbsnp": "rs2968804",
"frequency_reference_population": 0.6848217,
"hom_count_reference_population": 35524,
"allele_count_reference_population": 103556,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.684822,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 103556,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 35524,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.800000011920929,
"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": -0.8,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.152,
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000337526.11",
"gene_symbol": "RTN4",
"hgnc_id": 14085,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.3361-2598C>G",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}