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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: 12-48918375-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=48918375&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 48918375,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000320516.5",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DRC2",
"gene_hgnc_id": 29937,
"hgvs_c": "c.710C>T",
"hgvs_p": "p.Thr237Ile",
"transcript": "NM_033124.5",
"protein_id": "NP_149115.2",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 484,
"cds_start": 710,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 914,
"cdna_end": null,
"cdna_length": 1792,
"mane_select": "ENST00000320516.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "c.710C>T",
"hgvs_p": "p.Thr237Ile",
"transcript": "ENST00000320516.5",
"protein_id": "ENSP00000312706.4",
"transcript_support_level": 1,
"aa_start": 237,
"aa_end": null,
"aa_length": 484,
"cds_start": 710,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 914,
"cdna_end": null,
"cdna_length": 1792,
"mane_select": "NM_033124.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "ENSG00000272822",
"gene_hgnc_id": null,
"hgvs_c": "c.385-14467G>A",
"hgvs_p": null,
"transcript": "ENST00000398092.4",
"protein_id": "ENSP00000438507.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 210,
"cds_start": -4,
"cds_end": null,
"cds_length": 633,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 939,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "c.710C>T",
"hgvs_p": "p.Thr237Ile",
"transcript": "ENST00000266984.9",
"protein_id": "ENSP00000266984.5",
"transcript_support_level": 5,
"aa_start": 237,
"aa_end": null,
"aa_length": 497,
"cds_start": 710,
"cds_end": null,
"cds_length": 1494,
"cdna_start": 937,
"cdna_end": null,
"cdna_length": 2084,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "c.401C>T",
"hgvs_p": "p.Thr134Ile",
"transcript": "ENST00000552942.5",
"protein_id": "ENSP00000446569.1",
"transcript_support_level": 5,
"aa_start": 134,
"aa_end": null,
"aa_length": 372,
"cds_start": 401,
"cds_end": null,
"cds_length": 1120,
"cdna_start": 619,
"cdna_end": null,
"cdna_length": 1338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DRC2",
"gene_hgnc_id": 29937,
"hgvs_c": "c.281C>T",
"hgvs_p": "p.Thr94Ile",
"transcript": "NM_001286957.2",
"protein_id": "NP_001273886.1",
"transcript_support_level": null,
"aa_start": 94,
"aa_end": null,
"aa_length": 341,
"cds_start": 281,
"cds_end": null,
"cds_length": 1026,
"cdna_start": 874,
"cdna_end": null,
"cdna_length": 1752,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "n.*541C>T",
"hgvs_p": null,
"transcript": "ENST00000547861.5",
"protein_id": "ENSP00000447157.1",
"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": 1746,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "n.232C>T",
"hgvs_p": null,
"transcript": "ENST00000552188.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 582,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"hgvs_c": "n.*541C>T",
"hgvs_p": null,
"transcript": "ENST00000547861.5",
"protein_id": "ENSP00000447157.1",
"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": 1746,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CCDC65",
"gene_hgnc_id": 29937,
"dbsnp": "rs372541279",
"frequency_reference_population": 0.000037793456,
"hom_count_reference_population": 0,
"allele_count_reference_population": 61,
"gnomad_exomes_af": 0.0000396752,
"gnomad_genomes_af": 0.0000197153,
"gnomad_exomes_ac": 58,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5254455208778381,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.283,
"revel_prediction": "Benign",
"alphamissense_score": 0.5043,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 4.323,
"phylop100way_prediction": "Uncertain_significance",
"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": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "ENST00000320516.5",
"gene_symbol": "CCDC65",
"hgnc_id": 29937,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.710C>T",
"hgvs_p": "p.Thr237Ile"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000398092.4",
"gene_symbol": "ENSG00000272822",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.385-14467G>A",
"hgvs_p": null
},
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "NM_033124.5",
"gene_symbol": "DRC2",
"hgnc_id": 29937,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.710C>T",
"hgvs_p": "p.Thr237Ile"
}
],
"clinvar_disease": "Primary ciliary dyskinesia 27",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Primary ciliary dyskinesia 27",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}