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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: 6-32841603-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=32841603&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 32841603,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000374882.8",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "c.670G>T",
"hgvs_p": "p.Ala224Ser",
"transcript": "NM_148919.4",
"protein_id": "NP_683720.2",
"transcript_support_level": null,
"aa_start": 224,
"aa_end": null,
"aa_length": 276,
"cds_start": 670,
"cds_end": null,
"cds_length": 831,
"cdna_start": 721,
"cdna_end": null,
"cdna_length": 1124,
"mane_select": "ENST00000374882.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "c.670G>T",
"hgvs_p": "p.Ala224Ser",
"transcript": "ENST00000374882.8",
"protein_id": "ENSP00000364016.4",
"transcript_support_level": 1,
"aa_start": 224,
"aa_end": null,
"aa_length": 276,
"cds_start": 670,
"cds_end": null,
"cds_length": 831,
"cdna_start": 721,
"cdna_end": null,
"cdna_length": 1124,
"mane_select": "NM_148919.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "c.658G>T",
"hgvs_p": "p.Ala220Ser",
"transcript": "ENST00000374881.3",
"protein_id": "ENSP00000364015.2",
"transcript_support_level": 1,
"aa_start": 220,
"aa_end": null,
"aa_length": 272,
"cds_start": 658,
"cds_end": null,
"cds_length": 819,
"cdna_start": 924,
"cdna_end": null,
"cdna_length": 1327,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "c.658G>T",
"hgvs_p": "p.Ala220Ser",
"transcript": "NM_004159.5",
"protein_id": "NP_004150.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 272,
"cds_start": 658,
"cds_end": null,
"cds_length": 819,
"cdna_start": 924,
"cdna_end": null,
"cdna_length": 1327,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "c.598G>T",
"hgvs_p": "p.Ala200Ser",
"transcript": "ENST00000395339.7",
"protein_id": "ENSP00000378748.3",
"transcript_support_level": 3,
"aa_start": 200,
"aa_end": null,
"aa_length": 252,
"cds_start": 598,
"cds_end": null,
"cds_length": 759,
"cdna_start": 622,
"cdna_end": null,
"cdna_length": 1025,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "n.1054G>T",
"hgvs_p": null,
"transcript": "ENST00000484003.1",
"protein_id": null,
"transcript_support_level": 5,
"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": 1153,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "n.1991G>T",
"hgvs_p": null,
"transcript": "ENST00000650411.1",
"protein_id": null,
"transcript_support_level": null,
"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": 2373,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "n.1655G>T",
"hgvs_p": null,
"transcript": "ENST00000650793.2",
"protein_id": null,
"transcript_support_level": null,
"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": 2039,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"hgvs_c": "n.1527G>T",
"hgvs_p": null,
"transcript": "ENST00000697612.1",
"protein_id": null,
"transcript_support_level": null,
"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": 1896,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PSMB8",
"gene_hgnc_id": 9545,
"dbsnp": "rs114636648",
"frequency_reference_population": 0.0000619949,
"hom_count_reference_population": 0,
"allele_count_reference_population": 100,
"gnomad_exomes_af": 0.0000527126,
"gnomad_genomes_af": 0.000151032,
"gnomad_exomes_ac": 77,
"gnomad_genomes_ac": 23,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.44037941098213196,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.541,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.312,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.01,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 7.099,
"phylop100way_prediction": "Uncertain_significance",
"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": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "ENST00000374882.8",
"gene_symbol": "PSMB8",
"hgnc_id": 9545,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.670G>T",
"hgvs_p": "p.Ala224Ser"
}
],
"clinvar_disease": "Inborn genetic diseases,Proteosome-associated autoinflammatory syndrome,not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:3",
"phenotype_combined": "not provided|Proteosome-associated autoinflammatory syndrome|Inborn genetic diseases",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}