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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: 4-147639076-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=147639076&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 147639076,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_138364.4",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.2206A>C",
"hgvs_p": "p.Ile736Leu",
"transcript": "NM_138364.4",
"protein_id": "NP_612373.2",
"transcript_support_level": null,
"aa_start": 736,
"aa_end": null,
"aa_length": 845,
"cds_start": 2206,
"cds_end": null,
"cds_length": 2538,
"cdna_start": 2382,
"cdna_end": null,
"cdna_length": 3461,
"mane_select": "ENST00000322396.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.2206A>C",
"hgvs_p": "p.Ile736Leu",
"transcript": "ENST00000322396.7",
"protein_id": "ENSP00000314396.6",
"transcript_support_level": 1,
"aa_start": 736,
"aa_end": null,
"aa_length": 845,
"cds_start": 2206,
"cds_end": null,
"cds_length": 2538,
"cdna_start": 2382,
"cdna_end": null,
"cdna_length": 3461,
"mane_select": "NM_138364.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 8,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "TMEM184C",
"gene_hgnc_id": 25587,
"hgvs_c": "c.779+7571T>G",
"hgvs_p": null,
"transcript": "ENST00000508208.5",
"protein_id": "ENSP00000425940.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 261,
"cds_start": -4,
"cds_end": null,
"cds_length": 786,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1528,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.1867A>C",
"hgvs_p": "p.Ile623Leu",
"transcript": "NM_001304458.2",
"protein_id": "NP_001291387.1",
"transcript_support_level": null,
"aa_start": 623,
"aa_end": null,
"aa_length": 732,
"cds_start": 1867,
"cds_end": null,
"cds_length": 2199,
"cdna_start": 2233,
"cdna_end": null,
"cdna_length": 3312,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.1867A>C",
"hgvs_p": "p.Ile623Leu",
"transcript": "NM_001350142.2",
"protein_id": "NP_001337071.1",
"transcript_support_level": null,
"aa_start": 623,
"aa_end": null,
"aa_length": 732,
"cds_start": 1867,
"cds_end": null,
"cds_length": 2199,
"cdna_start": 2517,
"cdna_end": null,
"cdna_length": 3596,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.1291A>C",
"hgvs_p": "p.Ile431Leu",
"transcript": "NM_001350143.2",
"protein_id": "NP_001337072.1",
"transcript_support_level": null,
"aa_start": 431,
"aa_end": null,
"aa_length": 540,
"cds_start": 1291,
"cds_end": null,
"cds_length": 1623,
"cdna_start": 1961,
"cdna_end": null,
"cdna_length": 3040,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.1138A>C",
"hgvs_p": "p.Ile380Leu",
"transcript": "NM_001350141.2",
"protein_id": "NP_001337070.1",
"transcript_support_level": null,
"aa_start": 380,
"aa_end": null,
"aa_length": 489,
"cds_start": 1138,
"cds_end": null,
"cds_length": 1470,
"cdna_start": 2579,
"cdna_end": null,
"cdna_length": 3658,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.982A>C",
"hgvs_p": "p.Ile328Leu",
"transcript": "NM_001350144.2",
"protein_id": "NP_001337073.1",
"transcript_support_level": null,
"aa_start": 328,
"aa_end": null,
"aa_length": 437,
"cds_start": 982,
"cds_end": null,
"cds_length": 1314,
"cdna_start": 2228,
"cdna_end": null,
"cdna_length": 3307,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "c.1291A>C",
"hgvs_p": "p.Ile431Leu",
"transcript": "XM_047416393.1",
"protein_id": "XP_047272349.1",
"transcript_support_level": null,
"aa_start": 431,
"aa_end": null,
"aa_length": 540,
"cds_start": 1291,
"cds_end": null,
"cds_length": 1623,
"cdna_start": 1528,
"cdna_end": null,
"cdna_length": 2607,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "n.1533A>C",
"hgvs_p": null,
"transcript": "ENST00000510269.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2012,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"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": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "n.218A>C",
"hgvs_p": null,
"transcript": "ENST00000511687.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 401,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "n.*1856A>C",
"hgvs_p": null,
"transcript": "ENST00000514886.1",
"protein_id": "ENSP00000426732.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2674,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"hgvs_c": "n.*1856A>C",
"hgvs_p": null,
"transcript": "ENST00000514886.1",
"protein_id": "ENSP00000426732.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2674,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PRMT9",
"gene_hgnc_id": 25099,
"dbsnp": "rs1733206654",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09820687770843506,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.085,
"revel_prediction": "Benign",
"alphamissense_score": 0.1205,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.5,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.313,
"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_138364.4",
"gene_symbol": "PRMT9",
"hgnc_id": 25099,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2206A>C",
"hgvs_p": "p.Ile736Leu"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000508208.5",
"gene_symbol": "TMEM184C",
"hgnc_id": 25587,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.779+7571T>G",
"hgvs_p": null
}
],
"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
}