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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: 4-69944874-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=69944874&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 69944874,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001890.2",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Ala143Thr",
"transcript": "NM_001890.2",
"protein_id": "NP_001881.1",
"transcript_support_level": null,
"aa_start": 143,
"aa_end": null,
"aa_length": 185,
"cds_start": 427,
"cds_end": null,
"cds_length": 558,
"cdna_start": 489,
"cdna_end": null,
"cdna_length": 998,
"mane_select": "ENST00000246891.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Ala143Thr",
"transcript": "ENST00000246891.9",
"protein_id": "ENSP00000246891.4",
"transcript_support_level": 1,
"aa_start": 143,
"aa_end": null,
"aa_length": 185,
"cds_start": 427,
"cds_end": null,
"cds_length": 558,
"cdna_start": 489,
"cdna_end": null,
"cdna_length": 998,
"mane_select": "NM_001890.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.403G>A",
"hgvs_p": "p.Ala135Thr",
"transcript": "ENST00000507772.5",
"protein_id": "ENSP00000427490.1",
"transcript_support_level": 5,
"aa_start": 135,
"aa_end": null,
"aa_length": 177,
"cds_start": 403,
"cds_end": null,
"cds_length": 534,
"cdna_start": 403,
"cdna_end": null,
"cdna_length": 895,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.400G>A",
"hgvs_p": "p.Ala134Thr",
"transcript": "NM_001025104.2",
"protein_id": "NP_001020275.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 176,
"cds_start": 400,
"cds_end": null,
"cds_length": 531,
"cdna_start": 462,
"cdna_end": null,
"cdna_length": 971,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.400G>A",
"hgvs_p": "p.Ala134Thr",
"transcript": "ENST00000507763.5",
"protein_id": "ENSP00000422611.1",
"transcript_support_level": 5,
"aa_start": 134,
"aa_end": null,
"aa_length": 176,
"cds_start": 400,
"cds_end": null,
"cds_length": 531,
"cdna_start": 411,
"cdna_end": null,
"cdna_length": 597,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.379G>A",
"hgvs_p": "p.Ala127Thr",
"transcript": "ENST00000505782.5",
"protein_id": "ENSP00000426684.1",
"transcript_support_level": 5,
"aa_start": 127,
"aa_end": null,
"aa_length": 169,
"cds_start": 379,
"cds_end": null,
"cds_length": 510,
"cdna_start": 379,
"cdna_end": null,
"cdna_length": 871,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.100G>A",
"hgvs_p": "p.Ala34Thr",
"transcript": "ENST00000510936.1",
"protein_id": "ENSP00000421314.1",
"transcript_support_level": 3,
"aa_start": 34,
"aa_end": null,
"aa_length": 76,
"cds_start": 100,
"cds_end": null,
"cds_length": 231,
"cdna_start": 100,
"cdna_end": null,
"cdna_length": 596,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.424G>A",
"hgvs_p": "p.Ala142Thr",
"transcript": "XM_006714089.3",
"protein_id": "XP_006714152.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 184,
"cds_start": 424,
"cds_end": null,
"cds_length": 555,
"cdna_start": 486,
"cdna_end": null,
"cdna_length": 995,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.403G>A",
"hgvs_p": "p.Ala135Thr",
"transcript": "XM_006714090.3",
"protein_id": "XP_006714153.1",
"transcript_support_level": null,
"aa_start": 135,
"aa_end": null,
"aa_length": 177,
"cds_start": 403,
"cds_end": null,
"cds_length": 534,
"cdna_start": 465,
"cdna_end": null,
"cdna_length": 974,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"hgvs_c": "c.400G>A",
"hgvs_p": "p.Ala134Thr",
"transcript": "XM_006714091.3",
"protein_id": "XP_006714154.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 176,
"cds_start": 400,
"cds_end": null,
"cds_length": 531,
"cdna_start": 462,
"cdna_end": null,
"cdna_length": 971,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CSN1S1",
"gene_hgnc_id": 2445,
"dbsnp": "rs373734099",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": 0,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 0,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09758442640304565,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.034,
"revel_prediction": "Benign",
"alphamissense_score": 0.139,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.58,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.386,
"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_001890.2",
"gene_symbol": "CSN1S1",
"hgnc_id": 2445,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.427G>A",
"hgvs_p": "p.Ala143Thr"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}