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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: 11-65896990-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=65896990&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 65896990,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_005438.5",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "NM_005438.5",
"protein_id": "NP_005429.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 271,
"cds_start": 116,
"cds_end": null,
"cds_length": 816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000312562.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005438.5"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "ENST00000312562.7",
"protein_id": "ENSP00000310170.2",
"transcript_support_level": 1,
"aa_start": 39,
"aa_end": null,
"aa_length": 271,
"cds_start": 116,
"cds_end": null,
"cds_length": 816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_005438.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000312562.7"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "ENST00000531493.5",
"protein_id": "ENSP00000436276.1",
"transcript_support_level": 1,
"aa_start": 39,
"aa_end": null,
"aa_length": 235,
"cds_start": 116,
"cds_end": null,
"cds_length": 708,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000531493.5"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.113C>G",
"hgvs_p": "p.Pro38Arg",
"transcript": "ENST00000913992.1",
"protein_id": "ENSP00000584051.1",
"transcript_support_level": null,
"aa_start": 38,
"aa_end": null,
"aa_length": 270,
"cds_start": 113,
"cds_end": null,
"cds_length": 813,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913992.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "NM_001300844.2",
"protein_id": "NP_001287773.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 235,
"cds_start": 116,
"cds_end": null,
"cds_length": 708,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300844.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.113C>G",
"hgvs_p": "p.Pro38Arg",
"transcript": "ENST00000950881.1",
"protein_id": "ENSP00000620940.1",
"transcript_support_level": null,
"aa_start": 38,
"aa_end": null,
"aa_length": 234,
"cds_start": 113,
"cds_end": null,
"cds_length": 705,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950881.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "NM_001300855.2",
"protein_id": "NP_001287784.1",
"transcript_support_level": null,
"aa_start": 39,
"aa_end": null,
"aa_length": 135,
"cds_start": 116,
"cds_end": null,
"cds_length": 408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300855.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg",
"transcript": "ENST00000532401.1",
"protein_id": "ENSP00000431594.1",
"transcript_support_level": 2,
"aa_start": 39,
"aa_end": null,
"aa_length": 135,
"cds_start": 116,
"cds_end": null,
"cds_length": 408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000532401.1"
},
{
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.100-2869C>G",
"hgvs_p": null,
"transcript": "NM_001300856.2",
"protein_id": "NP_001287785.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 205,
"cds_start": null,
"cds_end": null,
"cds_length": 618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300856.2"
},
{
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.100-2869C>G",
"hgvs_p": null,
"transcript": "ENST00000913991.1",
"protein_id": "ENSP00000584050.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 205,
"cds_start": null,
"cds_end": null,
"cds_length": 618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913991.1"
},
{
"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": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.99+3251C>G",
"hgvs_p": null,
"transcript": "NM_001300857.2",
"protein_id": "NP_001287786.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 169,
"cds_start": null,
"cds_end": null,
"cds_length": 510,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300857.2"
},
{
"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": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.99+3251C>G",
"hgvs_p": null,
"transcript": "ENST00000448083.6",
"protein_id": "ENSP00000393302.2",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 169,
"cds_start": null,
"cds_end": null,
"cds_length": 510,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000448083.6"
},
{
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "c.-363-2869C>G",
"hgvs_p": null,
"transcript": "ENST00000534222.1",
"protein_id": "ENSP00000434350.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 11,
"cds_start": null,
"cds_end": null,
"cds_length": 38,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000534222.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"hgvs_c": "n.156-2869C>G",
"hgvs_p": null,
"transcript": "NR_125339.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_125339.2"
}
],
"gene_symbol": "FOSL1",
"gene_hgnc_id": 13718,
"dbsnp": "rs1457961074",
"frequency_reference_population": 0.000052671563,
"hom_count_reference_population": 0,
"allele_count_reference_population": 85,
"gnomad_exomes_af": 0.0000554191,
"gnomad_genomes_af": 0.000026284,
"gnomad_exomes_ac": 81,
"gnomad_genomes_ac": 4,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8577003479003906,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.803,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.4249,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.39,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.461,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.05,
"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": "PP3_Moderate,BS2",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PP3_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_005438.5",
"gene_symbol": "FOSL1",
"hgnc_id": 13718,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.116C>G",
"hgvs_p": "p.Pro39Arg"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}