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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: 17-49506586-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=49506586&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 49506586,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_002507.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NGFR",
"gene_hgnc_id": 7809,
"hgvs_c": "c.496C>T",
"hgvs_p": "p.Pro166Ser",
"transcript": "NM_002507.4",
"protein_id": "NP_002498.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 427,
"cds_start": 496,
"cds_end": null,
"cds_length": 1284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000172229.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002507.4"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NGFR",
"gene_hgnc_id": 7809,
"hgvs_c": "c.496C>T",
"hgvs_p": "p.Pro166Ser",
"transcript": "ENST00000172229.8",
"protein_id": "ENSP00000172229.3",
"transcript_support_level": 1,
"aa_start": 166,
"aa_end": null,
"aa_length": 427,
"cds_start": 496,
"cds_end": null,
"cds_length": 1284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002507.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000172229.8"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NGFR",
"gene_hgnc_id": 7809,
"hgvs_c": "c.214C>T",
"hgvs_p": "p.Pro72Ser",
"transcript": "ENST00000504201.1",
"protein_id": "ENSP00000421731.1",
"transcript_support_level": 2,
"aa_start": 72,
"aa_end": null,
"aa_length": 333,
"cds_start": 214,
"cds_end": null,
"cds_length": 1002,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000504201.1"
},
{
"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": 2,
"intron_rank_end": null,
"gene_symbol": "NGFR-AS1",
"gene_hgnc_id": 55555,
"hgvs_c": "n.378-86G>A",
"hgvs_p": null,
"transcript": "ENST00000514506.1",
"protein_id": null,
"transcript_support_level": 2,
"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": "ENST00000514506.1"
},
{
"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": 2,
"intron_rank_end": null,
"gene_symbol": "NGFR-AS1",
"gene_hgnc_id": 55555,
"hgvs_c": "n.378-86G>A",
"hgvs_p": null,
"transcript": "NR_103773.1",
"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_103773.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NGFR",
"gene_hgnc_id": 7809,
"hgvs_c": "c.*201C>T",
"hgvs_p": null,
"transcript": "ENST00000509200.5",
"protein_id": "ENSP00000421514.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 3,
"cds_start": null,
"cds_end": null,
"cds_length": 13,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000509200.5"
}
],
"gene_symbol": "NGFR",
"gene_hgnc_id": 7809,
"dbsnp": "rs372174350",
"frequency_reference_population": 0.000021260106,
"hom_count_reference_population": 0,
"allele_count_reference_population": 31,
"gnomad_exomes_af": 0.0000212601,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 31,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8769271373748779,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.724,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.969,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.08,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 7.752,
"phylop100way_prediction": "Pathogenic",
"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": "PP3_Moderate,BS2",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PP3_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_002507.4",
"gene_symbol": "NGFR",
"hgnc_id": 7809,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.496C>T",
"hgvs_p": "p.Pro166Ser"
},
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000514506.1",
"gene_symbol": "NGFR-AS1",
"hgnc_id": 55555,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.378-86G>A",
"hgvs_p": null
}
],
"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
}