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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: 12-101765032-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=101765032&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 101765032,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_024312.5",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1885A>T",
"hgvs_p": "p.Ile629Leu",
"transcript": "NM_024312.5",
"protein_id": "NP_077288.2",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 1256,
"cds_start": 1885,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000299314.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_024312.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1885A>T",
"hgvs_p": "p.Ile629Leu",
"transcript": "ENST00000299314.12",
"protein_id": "ENSP00000299314.7",
"transcript_support_level": 1,
"aa_start": 629,
"aa_end": null,
"aa_length": 1256,
"cds_start": 1885,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_024312.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000299314.12"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1906A>T",
"hgvs_p": "p.Ile636Leu",
"transcript": "ENST00000917136.1",
"protein_id": "ENSP00000587195.1",
"transcript_support_level": null,
"aa_start": 636,
"aa_end": null,
"aa_length": 1263,
"cds_start": 1906,
"cds_end": null,
"cds_length": 3792,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917136.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1879A>T",
"hgvs_p": "p.Ile627Leu",
"transcript": "ENST00000917134.1",
"protein_id": "ENSP00000587193.1",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 1254,
"cds_start": 1879,
"cds_end": null,
"cds_length": 3765,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917134.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1765A>T",
"hgvs_p": "p.Ile589Leu",
"transcript": "ENST00000917133.1",
"protein_id": "ENSP00000587192.1",
"transcript_support_level": null,
"aa_start": 589,
"aa_end": null,
"aa_length": 1216,
"cds_start": 1765,
"cds_end": null,
"cds_length": 3651,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917133.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1732A>T",
"hgvs_p": "p.Ile578Leu",
"transcript": "ENST00000917135.1",
"protein_id": "ENSP00000587194.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 1205,
"cds_start": 1732,
"cds_end": null,
"cds_length": 3618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917135.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1681A>T",
"hgvs_p": "p.Ile561Leu",
"transcript": "ENST00000953730.1",
"protein_id": "ENSP00000623789.1",
"transcript_support_level": null,
"aa_start": 561,
"aa_end": null,
"aa_length": 1188,
"cds_start": 1681,
"cds_end": null,
"cds_length": 3567,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953730.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1804A>T",
"hgvs_p": "p.Ile602Leu",
"transcript": "XM_011538731.3",
"protein_id": "XP_011537033.1",
"transcript_support_level": null,
"aa_start": 602,
"aa_end": null,
"aa_length": 1229,
"cds_start": 1804,
"cds_end": null,
"cds_length": 3690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538731.3"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"hgvs_c": "c.1885A>T",
"hgvs_p": "p.Ile629Leu",
"transcript": "XM_006719593.4",
"protein_id": "XP_006719656.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 1179,
"cds_start": 1885,
"cds_end": null,
"cds_length": 3540,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719593.4"
}
],
"gene_symbol": "GNPTAB",
"gene_hgnc_id": 29670,
"dbsnp": "rs374265672",
"frequency_reference_population": 0.0000061953033,
"hom_count_reference_population": 0,
"allele_count_reference_population": 10,
"gnomad_exomes_af": 0.0000061565,
"gnomad_genomes_af": 0.00000656789,
"gnomad_exomes_ac": 9,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0825408399105072,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.284,
"revel_prediction": "Benign",
"alphamissense_score": 0.0729,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.19,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.129,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_024312.5",
"gene_symbol": "GNPTAB",
"hgnc_id": 29670,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1885A>T",
"hgvs_p": "p.Ile629Leu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}