← Back to variant description
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: 3-191380893-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=191380893&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 191380893,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "NM_178335.3",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.1203A>G",
"hgvs_p": "p.Lys401Lys",
"transcript": "NM_178335.3",
"protein_id": "NP_848018.1",
"transcript_support_level": null,
"aa_start": 401,
"aa_end": null,
"aa_length": 482,
"cds_start": 1203,
"cds_end": null,
"cds_length": 1449,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000392455.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_178335.3"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.1203A>G",
"hgvs_p": "p.Lys401Lys",
"transcript": "ENST00000392455.9",
"protein_id": "ENSP00000376249.4",
"transcript_support_level": 1,
"aa_start": 401,
"aa_end": null,
"aa_length": 482,
"cds_start": 1203,
"cds_end": null,
"cds_length": 1449,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_178335.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392455.9"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.675A>G",
"hgvs_p": "p.Lys225Lys",
"transcript": "ENST00000392456.4",
"protein_id": "ENSP00000376250.4",
"transcript_support_level": 1,
"aa_start": 225,
"aa_end": null,
"aa_length": 306,
"cds_start": 675,
"cds_end": null,
"cds_length": 921,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392456.4"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.1290A>G",
"hgvs_p": "p.Lys430Lys",
"transcript": "ENST00000899243.1",
"protein_id": "ENSP00000569302.1",
"transcript_support_level": null,
"aa_start": 430,
"aa_end": null,
"aa_length": 511,
"cds_start": 1290,
"cds_end": null,
"cds_length": 1536,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899243.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.1158A>G",
"hgvs_p": "p.Lys386Lys",
"transcript": "ENST00000951804.1",
"protein_id": "ENSP00000621863.1",
"transcript_support_level": null,
"aa_start": 386,
"aa_end": null,
"aa_length": 467,
"cds_start": 1158,
"cds_end": null,
"cds_length": 1404,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951804.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.1140A>G",
"hgvs_p": "p.Lys380Lys",
"transcript": "ENST00000899246.1",
"protein_id": "ENSP00000569305.1",
"transcript_support_level": null,
"aa_start": 380,
"aa_end": null,
"aa_length": 461,
"cds_start": 1140,
"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": "ENST00000899246.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.762A>G",
"hgvs_p": "p.Lys254Lys",
"transcript": "ENST00000899245.1",
"protein_id": "ENSP00000569304.1",
"transcript_support_level": null,
"aa_start": 254,
"aa_end": null,
"aa_length": 335,
"cds_start": 762,
"cds_end": null,
"cds_length": 1008,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899245.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.756A>G",
"hgvs_p": "p.Lys252Lys",
"transcript": "ENST00000951803.1",
"protein_id": "ENSP00000621862.1",
"transcript_support_level": null,
"aa_start": 252,
"aa_end": null,
"aa_length": 333,
"cds_start": 756,
"cds_end": null,
"cds_length": 1002,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951803.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.675A>G",
"hgvs_p": "p.Lys225Lys",
"transcript": "ENST00000951802.1",
"protein_id": "ENSP00000621861.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 320,
"cds_start": 675,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951802.1"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.675A>G",
"hgvs_p": "p.Lys225Lys",
"transcript": "NM_174908.4",
"protein_id": "NP_777568.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 306,
"cds_start": 675,
"cds_end": null,
"cds_length": 921,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_174908.4"
},
{
"aa_ref": "K",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"hgvs_c": "c.612A>G",
"hgvs_p": "p.Lys204Lys",
"transcript": "ENST00000899244.1",
"protein_id": "ENSP00000569303.1",
"transcript_support_level": null,
"aa_start": 204,
"aa_end": null,
"aa_length": 285,
"cds_start": 612,
"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": "ENST00000899244.1"
}
],
"gene_symbol": "CCDC50",
"gene_hgnc_id": 18111,
"dbsnp": "rs146511344",
"frequency_reference_population": 0.0021854474,
"hom_count_reference_population": 7,
"allele_count_reference_population": 3525,
"gnomad_exomes_af": 0.00224962,
"gnomad_genomes_af": 0.00156981,
"gnomad_exomes_ac": 3286,
"gnomad_genomes_ac": 239,
"gnomad_exomes_homalt": 7,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8100000023841858,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.81,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.455,
"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": -17,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2",
"acmg_by_gene": [
{
"score": -17,
"benign_score": 17,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_178335.3",
"gene_symbol": "CCDC50",
"hgnc_id": 18111,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.1203A>G",
"hgvs_p": "p.Lys401Lys"
}
],
"clinvar_disease": "CCDC50-related disorder,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:4 B:2",
"phenotype_combined": "not specified|not provided|CCDC50-related disorder",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}