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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: 3-132675903-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=132675903&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 132675903,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_024818.6",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1111G>A",
"hgvs_p": "p.Ala371Thr",
"transcript": "NM_024818.6",
"protein_id": "NP_079094.1",
"transcript_support_level": null,
"aa_start": 371,
"aa_end": null,
"aa_length": 404,
"cds_start": 1111,
"cds_end": null,
"cds_length": 1215,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000356232.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_024818.6"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1111G>A",
"hgvs_p": "p.Ala371Thr",
"transcript": "ENST00000356232.10",
"protein_id": "ENSP00000348565.4",
"transcript_support_level": 1,
"aa_start": 371,
"aa_end": null,
"aa_length": 404,
"cds_start": 1111,
"cds_end": null,
"cds_length": 1215,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_024818.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000356232.10"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.943G>A",
"hgvs_p": "p.Ala315Thr",
"transcript": "ENST00000494238.6",
"protein_id": "ENSP00000418807.2",
"transcript_support_level": 1,
"aa_start": 315,
"aa_end": null,
"aa_length": 348,
"cds_start": 943,
"cds_end": null,
"cds_length": 1047,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000494238.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "NPHP3-ACAD11",
"gene_hgnc_id": 48351,
"hgvs_c": "c.635+6011C>T",
"hgvs_p": null,
"transcript": "ENST00000632629.1",
"protein_id": "ENSP00000488520.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 230,
"cds_start": null,
"cds_end": null,
"cds_length": 694,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000632629.1"
},
{
"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": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1282G>A",
"hgvs_p": "p.Ala428Thr",
"transcript": "ENST00000683741.1",
"protein_id": "ENSP00000507396.1",
"transcript_support_level": null,
"aa_start": 428,
"aa_end": null,
"aa_length": 461,
"cds_start": 1282,
"cds_end": null,
"cds_length": 1386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000683741.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1054G>A",
"hgvs_p": "p.Ala352Thr",
"transcript": "ENST00000967272.1",
"protein_id": "ENSP00000637331.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 385,
"cds_start": 1054,
"cds_end": null,
"cds_length": 1158,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967272.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1111G>A",
"hgvs_p": "p.Ala371Thr",
"transcript": "ENST00000493720.6",
"protein_id": "ENSP00000417879.2",
"transcript_support_level": 5,
"aa_start": 371,
"aa_end": null,
"aa_length": 377,
"cds_start": 1111,
"cds_end": null,
"cds_length": 1134,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000493720.6"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1006G>A",
"hgvs_p": "p.Ala336Thr",
"transcript": "ENST00000967273.1",
"protein_id": "ENSP00000637332.1",
"transcript_support_level": null,
"aa_start": 336,
"aa_end": null,
"aa_length": 369,
"cds_start": 1006,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967273.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.943G>A",
"hgvs_p": "p.Ala315Thr",
"transcript": "NM_001320210.2",
"protein_id": "NP_001307139.1",
"transcript_support_level": null,
"aa_start": 315,
"aa_end": null,
"aa_length": 348,
"cds_start": 943,
"cds_end": null,
"cds_length": 1047,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001320210.2"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.943G>A",
"hgvs_p": "p.Ala315Thr",
"transcript": "NM_198329.4",
"protein_id": "NP_938143.1",
"transcript_support_level": null,
"aa_start": 315,
"aa_end": null,
"aa_length": 348,
"cds_start": 943,
"cds_end": null,
"cds_length": 1047,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_198329.4"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.943G>A",
"hgvs_p": "p.Ala315Thr",
"transcript": "ENST00000264991.8",
"protein_id": "ENSP00000264991.4",
"transcript_support_level": 5,
"aa_start": 315,
"aa_end": null,
"aa_length": 348,
"cds_start": 943,
"cds_end": null,
"cds_length": 1047,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000264991.8"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.841G>A",
"hgvs_p": "p.Ala281Thr",
"transcript": "NM_001321238.2",
"protein_id": "NP_001308167.1",
"transcript_support_level": null,
"aa_start": 281,
"aa_end": null,
"aa_length": 314,
"cds_start": 841,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001321238.2"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.775G>A",
"hgvs_p": "p.Ala259Thr",
"transcript": "NM_001321239.1",
"protein_id": "NP_001308168.1",
"transcript_support_level": null,
"aa_start": 259,
"aa_end": null,
"aa_length": 292,
"cds_start": 775,
"cds_end": null,
"cds_length": 879,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001321239.1"
},
{
"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": 11,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "c.1024+223G>A",
"hgvs_p": null,
"transcript": "ENST00000473651.5",
"protein_id": "ENSP00000424984.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 347,
"cds_start": null,
"cds_end": null,
"cds_length": 1044,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000473651.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "n.2542G>A",
"hgvs_p": null,
"transcript": "ENST00000468227.5",
"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": "retained_intron",
"feature": "ENST00000468227.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "n.386G>A",
"hgvs_p": null,
"transcript": "ENST00000494112.1",
"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": "retained_intron",
"feature": "ENST00000494112.1"
},
{
"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": 45,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "NPHP3-ACAD11",
"gene_hgnc_id": 48351,
"hgvs_c": "n.*1980+6011C>T",
"hgvs_p": null,
"transcript": "ENST00000471702.2",
"protein_id": "ENSP00000419763.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000471702.2"
},
{
"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": 45,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "NPHP3-ACAD11",
"gene_hgnc_id": 48351,
"hgvs_c": "n.3995+6011C>T",
"hgvs_p": null,
"transcript": "NR_037804.1",
"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_037804.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"hgvs_c": "n.*47G>A",
"hgvs_p": null,
"transcript": "XR_007095728.1",
"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": "XR_007095728.1"
}
],
"gene_symbol": "UBA5",
"gene_hgnc_id": 23230,
"dbsnp": "rs114925667",
"frequency_reference_population": 0.0026954683,
"hom_count_reference_population": 7,
"allele_count_reference_population": 4316,
"gnomad_exomes_af": 0.00280852,
"gnomad_genomes_af": 0.00161797,
"gnomad_exomes_ac": 4070,
"gnomad_genomes_ac": 246,
"gnomad_exomes_homalt": 6,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.012316882610321045,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.679,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.3109,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.13,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 8.94,
"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": 6,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PS3,PP5_Very_Strong,BP4,BS1_Supporting,BS2",
"acmg_by_gene": [
{
"score": 6,
"benign_score": 6,
"pathogenic_score": 12,
"criteria": [
"PS3",
"PP5_Very_Strong",
"BP4",
"BS1_Supporting",
"BS2"
],
"verdict": "Likely_pathogenic",
"transcript": "NM_024818.6",
"gene_symbol": "UBA5",
"hgnc_id": 23230,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.1111G>A",
"hgvs_p": "p.Ala371Thr"
},
{
"score": 7,
"benign_score": 5,
"pathogenic_score": 12,
"criteria": [
"PS3",
"PP5_Very_Strong",
"BP4",
"BS2"
],
"verdict": "Likely_pathogenic",
"transcript": "ENST00000632629.1",
"gene_symbol": "NPHP3-ACAD11",
"hgnc_id": 48351,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.635+6011C>T",
"hgvs_p": null
}
],
"clinvar_disease": " 44, autosomal recessive 24,Developmental and epileptic encephalopathy,Intellectual disability,Spinocerebellar ataxia,UBA5-related disorder,not provided",
"clinvar_classification": " low penetrance,Pathogenic/Likely pathogenic/Pathogenic",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:18 LP:1",
"phenotype_combined": "Developmental and epileptic encephalopathy, 44|not provided|Developmental and epileptic encephalopathy, 44;Spinocerebellar ataxia, autosomal recessive 24|Developmental and epileptic encephalopathy|UBA5-related disorder|Intellectual disability",
"pathogenicity_classification_combined": "Pathogenic/Likely pathogenic/Pathogenic, low penetrance",
"custom_annotations": null
}
],
"message": null
}