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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: 1-149944089-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=149944089&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 149944089,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_020205.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "NM_020205.4",
"protein_id": "NP_064590.2",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000581312.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_020205.4"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "ENST00000581312.6",
"protein_id": "ENSP00000462729.1",
"transcript_support_level": 1,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_020205.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000581312.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "ENST00000907908.1",
"protein_id": "ENSP00000577967.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907908.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "ENST00000907909.1",
"protein_id": "ENSP00000577968.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907909.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "ENST00000907910.1",
"protein_id": "ENSP00000577969.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907910.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "ENST00000907911.1",
"protein_id": "ENSP00000577970.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907911.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "ENST00000907913.1",
"protein_id": "ENSP00000577972.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907913.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2225C>G",
"hgvs_p": "p.Pro742Arg",
"transcript": "ENST00000907912.1",
"protein_id": "ENSP00000577971.1",
"transcript_support_level": null,
"aa_start": 742,
"aa_end": null,
"aa_length": 818,
"cds_start": 2225,
"cds_end": null,
"cds_length": 2457,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000907912.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_011509782.2",
"protein_id": "XP_011508084.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011509782.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_011509784.4",
"protein_id": "XP_011508086.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011509784.4"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_011509785.3",
"protein_id": "XP_011508087.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011509785.3"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_047425712.1",
"protein_id": "XP_047281668.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425712.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_047425715.1",
"protein_id": "XP_047281671.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425715.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2327C>G",
"hgvs_p": "p.Pro776Arg",
"transcript": "XM_047425716.1",
"protein_id": "XP_047281672.1",
"transcript_support_level": null,
"aa_start": 776,
"aa_end": null,
"aa_length": 852,
"cds_start": 2327,
"cds_end": null,
"cds_length": 2559,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425716.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "XM_047425717.1",
"protein_id": "XP_047281673.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425717.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "XM_047425720.1",
"protein_id": "XP_047281676.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425720.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg",
"transcript": "XM_047425721.1",
"protein_id": "XP_047281677.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 843,
"cds_start": 2300,
"cds_end": null,
"cds_length": 2532,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047425721.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2090C>G",
"hgvs_p": "p.Pro697Arg",
"transcript": "XM_011509788.3",
"protein_id": "XP_011508090.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 773,
"cds_start": 2090,
"cds_end": null,
"cds_length": 2322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011509788.3"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"hgvs_c": "c.2063C>G",
"hgvs_p": "p.Pro688Arg",
"transcript": "XM_017001850.2",
"protein_id": "XP_016857339.1",
"transcript_support_level": null,
"aa_start": 688,
"aa_end": null,
"aa_length": 764,
"cds_start": 2063,
"cds_end": null,
"cds_length": 2295,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017001850.2"
}
],
"gene_symbol": "OTUD7B",
"gene_hgnc_id": 16683,
"dbsnp": "rs782283906",
"frequency_reference_population": 6.8408156e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84082e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.08928218483924866,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.044,
"revel_prediction": "Benign",
"alphamissense_score": 0.0808,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.56,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.555,
"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_020205.4",
"gene_symbol": "OTUD7B",
"hgnc_id": 16683,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2300C>G",
"hgvs_p": "p.Pro767Arg"
}
],
"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
}