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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: 9-128332233-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=128332233&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 128332233,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_016035.5",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.483G>C",
"hgvs_p": "p.Glu161Asp",
"transcript": "NM_016035.5",
"protein_id": "NP_057119.3",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 265,
"cds_start": 483,
"cds_end": null,
"cds_length": 798,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000300452.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016035.5"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.483G>C",
"hgvs_p": "p.Glu161Asp",
"transcript": "ENST00000300452.8",
"protein_id": "ENSP00000300452.3",
"transcript_support_level": 1,
"aa_start": 161,
"aa_end": null,
"aa_length": 265,
"cds_start": 483,
"cds_end": null,
"cds_length": 798,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_016035.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000300452.8"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.543G>C",
"hgvs_p": "p.Glu181Asp",
"transcript": "ENST00000926106.1",
"protein_id": "ENSP00000596165.1",
"transcript_support_level": null,
"aa_start": 181,
"aa_end": null,
"aa_length": 285,
"cds_start": 543,
"cds_end": null,
"cds_length": 858,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926106.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.534G>C",
"hgvs_p": "p.Glu178Asp",
"transcript": "ENST00000926105.1",
"protein_id": "ENSP00000596164.1",
"transcript_support_level": null,
"aa_start": 178,
"aa_end": null,
"aa_length": 282,
"cds_start": 534,
"cds_end": null,
"cds_length": 849,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926105.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.498G>C",
"hgvs_p": "p.Glu166Asp",
"transcript": "ENST00000926108.1",
"protein_id": "ENSP00000596167.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 270,
"cds_start": 498,
"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": "ENST00000926108.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.489G>C",
"hgvs_p": "p.Glu163Asp",
"transcript": "ENST00000970497.1",
"protein_id": "ENSP00000640556.1",
"transcript_support_level": null,
"aa_start": 163,
"aa_end": null,
"aa_length": 267,
"cds_start": 489,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970497.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.414G>C",
"hgvs_p": "p.Glu138Asp",
"transcript": "ENST00000861346.1",
"protein_id": "ENSP00000531405.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 242,
"cds_start": 414,
"cds_end": null,
"cds_length": 729,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861346.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.399G>C",
"hgvs_p": "p.Glu133Asp",
"transcript": "ENST00000861347.1",
"protein_id": "ENSP00000531406.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 237,
"cds_start": 399,
"cds_end": null,
"cds_length": 714,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861347.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.315G>C",
"hgvs_p": "p.Glu105Asp",
"transcript": "ENST00000926107.1",
"protein_id": "ENSP00000596166.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 209,
"cds_start": 315,
"cds_end": null,
"cds_length": 630,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926107.1"
},
{
"aa_ref": "E",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.270G>C",
"hgvs_p": "p.Glu90Asp",
"transcript": "ENST00000926109.1",
"protein_id": "ENSP00000596168.1",
"transcript_support_level": null,
"aa_start": 90,
"aa_end": null,
"aa_length": 194,
"cds_start": 270,
"cds_end": null,
"cds_length": 585,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926109.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.*83G>C",
"hgvs_p": null,
"transcript": "XM_047423449.1",
"protein_id": "XP_047279405.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 100,
"cds_start": null,
"cds_end": null,
"cds_length": 303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047423449.1"
},
{
"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": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.353-617G>C",
"hgvs_p": null,
"transcript": "ENST00000926110.1",
"protein_id": "ENSP00000596169.1",
"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": "ENST00000926110.1"
},
{
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.203-617G>C",
"hgvs_p": null,
"transcript": "ENST00000861345.1",
"protein_id": "ENSP00000531404.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": null,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861345.1"
},
{
"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": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.*3-1241G>C",
"hgvs_p": null,
"transcript": "NM_001305942.2",
"protein_id": "NP_001292871.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 100,
"cds_start": null,
"cds_end": null,
"cds_length": 303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001305942.2"
},
{
"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": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "c.*3-617G>C",
"hgvs_p": null,
"transcript": "XM_017014792.2",
"protein_id": "XP_016870281.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 100,
"cds_start": null,
"cds_end": null,
"cds_length": 303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017014792.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"hgvs_c": "n.1822G>C",
"hgvs_p": null,
"transcript": "ENST00000461102.1",
"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": "ENST00000461102.1"
}
],
"gene_symbol": "COQ4",
"gene_hgnc_id": 19693,
"dbsnp": "rs141228574",
"frequency_reference_population": 0.008109713,
"hom_count_reference_population": 91,
"allele_count_reference_population": 13084,
"gnomad_exomes_af": 0.00837667,
"gnomad_genomes_af": 0.00554855,
"gnomad_exomes_ac": 12239,
"gnomad_genomes_ac": 845,
"gnomad_exomes_homalt": 85,
"gnomad_genomes_homalt": 6,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.018062353134155273,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.448,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.884,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.12,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 0.884,
"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": -18,
"acmg_classification": "Benign",
"acmg_criteria": "PM1,BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -18,
"benign_score": 20,
"pathogenic_score": 2,
"criteria": [
"PM1",
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_016035.5",
"gene_symbol": "COQ4",
"hgnc_id": 19693,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.483G>C",
"hgvs_p": "p.Glu161Asp"
}
],
"clinvar_disease": "Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:1 B:3",
"phenotype_combined": "not specified|Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome|not provided",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}