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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: 3-11287399-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=11287399&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 11287399,
"ref": "A",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000693202.1",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-11+4961A>T",
"hgvs_p": null,
"transcript": "NM_001349232.2",
"protein_id": "NP_001336161.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5333,
"mane_select": "ENST00000693202.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-11+4961A>T",
"hgvs_p": null,
"transcript": "ENST00000693202.1",
"protein_id": "ENSP00000510336.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5333,
"mane_select": "NM_001349232.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-10-11287A>T",
"hgvs_p": null,
"transcript": "ENST00000354449.7",
"protein_id": "ENSP00000346437.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4959,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-10-11287A>T",
"hgvs_p": null,
"transcript": "ENST00000354956.9",
"protein_id": "ENSP00000347042.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 676,
"cds_start": -4,
"cds_end": null,
"cds_length": 2031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2296,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "n.50-11287A>T",
"hgvs_p": null,
"transcript": "ENST00000470474.1",
"protein_id": null,
"transcript_support_level": 1,
"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": 534,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-11+6297A>T",
"hgvs_p": null,
"transcript": "NM_001349233.2",
"protein_id": "NP_001336162.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5087,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-105-1247A>T",
"hgvs_p": null,
"transcript": "NM_001349234.2",
"protein_id": "NP_001336163.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"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": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-11+4961A>T",
"hgvs_p": null,
"transcript": "NM_001349235.2",
"protein_id": "NP_001336164.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5224,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-10-11287A>T",
"hgvs_p": null,
"transcript": "NM_006395.3",
"protein_id": "NP_006386.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 703,
"cds_start": -4,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4978,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-11+6297A>T",
"hgvs_p": null,
"transcript": "ENST00000685771.1",
"protein_id": "ENSP00000509725.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 703,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 18,
"intron_rank": 1,
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"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "c.-10-11287A>T",
"hgvs_p": null,
"transcript": "NM_001136031.3",
"protein_id": "NP_001129503.2",
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},
{
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"protein_coding": true,
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"consequences": [
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],
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-10-11287A>T",
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"transcript": "NM_001349236.2",
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},
{
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],
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-10-11287A>T",
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"transcript": "NM_001349237.2",
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},
{
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],
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-10-11287A>T",
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"transcript": "NM_001144912.2",
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},
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],
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},
{
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"strand": true,
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],
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"intron_rank": 1,
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"gene_symbol": "ATG7",
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},
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],
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-11+4961A>T",
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"transcript": "ENST00000451513.5",
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},
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],
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"intron_rank": 1,
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-10-11287A>T",
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"transcript": "ENST00000451830.5",
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},
{
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],
"exon_rank": null,
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"exon_count": 5,
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"gene_symbol": "ATG7",
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"hgvs_c": "c.-11+9980A>T",
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"transcript": "ENST00000423116.1",
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},
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],
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"transcript": "ENST00000444619.5",
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},
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],
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},
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],
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"intron_rank": 1,
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"gene_symbol": "ATG7",
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"hgvs_c": "n.-10-11287A>T",
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"transcript": "ENST00000418682.5",
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 20,
"intron_rank": 3,
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"gene_symbol": "ATG7",
"gene_hgnc_id": 16935,
"hgvs_c": "n.-11+4961A>T",
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"transcript": "ENST00000435760.6",
"protein_id": "ENSP00000390547.2",
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},
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},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
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"intron_variant"
],
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"gene_symbol": "ATG7",
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}
],
"gene_symbol": "ATG7",
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"dbsnp": "rs346081",
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"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8899999856948853,
"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": -0.89,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.328,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000693202.1",
"gene_symbol": "ATG7",
"hgnc_id": 16935,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.-11+4961A>T",
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}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}