← Back to variant description
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: 5-620195-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=620195&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 620195,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_018140.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "NM_018140.4",
"protein_id": "NP_060610.2",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 2366,
"mane_select": "ENST00000264935.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_018140.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "ENST00000264935.6",
"protein_id": "ENSP00000264935.5",
"transcript_support_level": 1,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 2366,
"mane_select": "NM_018140.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000264935.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.-122G>A",
"hgvs_p": null,
"transcript": "XM_047417368.1",
"protein_id": "XP_047273324.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 458,
"cds_start": null,
"cds_end": null,
"cds_length": 1377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 15774,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417368.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "ENST00000856935.1",
"protein_id": "ENSP00000526994.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 362,
"cdna_end": null,
"cdna_length": 3631,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000856935.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "ENST00000919286.1",
"protein_id": "ENSP00000589345.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 576,
"cds_start": 337,
"cds_end": null,
"cds_length": 1731,
"cdna_start": 353,
"cdna_end": null,
"cdna_length": 2298,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919286.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "ENST00000919287.1",
"protein_id": "ENSP00000589346.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 551,
"cds_start": 337,
"cds_end": null,
"cds_length": 1656,
"cdna_start": 369,
"cdna_end": null,
"cdna_length": 2093,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919287.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "ENST00000919288.1",
"protein_id": "ENSP00000589347.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 536,
"cds_start": 337,
"cds_end": null,
"cds_length": 1611,
"cdna_start": 362,
"cdna_end": null,
"cdna_length": 2041,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919288.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "XM_011514063.2",
"protein_id": "XP_011512365.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 13667,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514063.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "XM_047417363.1",
"protein_id": "XP_047273319.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 16219,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417363.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "XM_047417364.1",
"protein_id": "XP_047273320.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 13955,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417364.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "XM_047417365.1",
"protein_id": "XP_047273321.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 13796,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417365.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met",
"transcript": "XM_047417366.1",
"protein_id": "XP_047273322.1",
"transcript_support_level": null,
"aa_start": 113,
"aa_end": null,
"aa_length": 647,
"cds_start": 337,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 359,
"cdna_end": null,
"cdna_length": 2294,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417366.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.187G>A",
"hgvs_p": "p.Val63Met",
"transcript": "XM_005248322.4",
"protein_id": "XP_005248379.1",
"transcript_support_level": null,
"aa_start": 63,
"aa_end": null,
"aa_length": 597,
"cds_start": 187,
"cds_end": null,
"cds_length": 1794,
"cdna_start": 318,
"cdna_end": null,
"cdna_length": 16178,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005248322.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.187G>A",
"hgvs_p": "p.Val63Met",
"transcript": "XM_011514064.3",
"protein_id": "XP_011512366.1",
"transcript_support_level": null,
"aa_start": 63,
"aa_end": null,
"aa_length": 597,
"cds_start": 187,
"cds_end": null,
"cds_length": 1794,
"cdna_start": 384,
"cdna_end": null,
"cdna_length": 16244,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514064.3"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.187G>A",
"hgvs_p": "p.Val63Met",
"transcript": "XM_047417367.1",
"protein_id": "XP_047273323.1",
"transcript_support_level": null,
"aa_start": 63,
"aa_end": null,
"aa_length": 597,
"cds_start": 187,
"cds_end": null,
"cds_length": 1794,
"cdna_start": 276,
"cdna_end": null,
"cdna_length": 16136,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417367.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.-122G>A",
"hgvs_p": null,
"transcript": "XM_047417368.1",
"protein_id": "XP_047273324.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 458,
"cds_start": null,
"cds_end": null,
"cds_length": 1377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 15774,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417368.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.82+7752G>A",
"hgvs_p": null,
"transcript": "ENST00000919290.1",
"protein_id": "ENSP00000589349.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 373,
"cds_start": null,
"cds_end": null,
"cds_length": 1122,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1538,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919290.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "c.82+7752G>A",
"hgvs_p": null,
"transcript": "ENST00000919289.1",
"protein_id": "ENSP00000589348.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 119,
"cds_start": null,
"cds_end": null,
"cds_length": 360,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 785,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919289.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"hgvs_c": "n.517G>A",
"hgvs_p": null,
"transcript": "NR_164122.1",
"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": 4475,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_164122.1"
}
],
"gene_symbol": "CEP72",
"gene_hgnc_id": 25547,
"dbsnp": "rs776619865",
"frequency_reference_population": 0.000013009718,
"hom_count_reference_population": 1,
"allele_count_reference_population": 21,
"gnomad_exomes_af": 0.0000136809,
"gnomad_genomes_af": 0.00000656642,
"gnomad_exomes_ac": 20,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.40400007367134094,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.07000000029802322,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.278,
"revel_prediction": "Benign",
"alphamissense_score": 0.5886,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": -0.18,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.981,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.07,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_018140.4",
"gene_symbol": "CEP72",
"hgnc_id": 25547,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.337G>A",
"hgvs_p": "p.Val113Met"
}
],
"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
}