← 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: 5-36955469-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=36955469&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 36955469,
"ref": "T",
"alt": "G",
"effect": "splice_region_variant,intron_variant",
"transcript": "ENST00000282516.13",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 47,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "NM_133433.4",
"protein_id": "NP_597677.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2804,
"cds_start": -4,
"cds_end": null,
"cds_length": 8415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10425,
"mane_select": "ENST00000282516.13",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 47,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "ENST00000282516.13",
"protein_id": "ENSP00000282516.8",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2804,
"cds_start": -4,
"cds_end": null,
"cds_length": 8415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10425,
"mane_select": "NM_133433.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "ENST00000448238.2",
"protein_id": "ENSP00000406266.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2697,
"cds_start": -4,
"cds_end": null,
"cds_length": 8094,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8729,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 47,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "NM_001438586.1",
"protein_id": "NP_001425515.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2698,
"cds_start": -4,
"cds_end": null,
"cds_length": 8097,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "NM_015384.5",
"protein_id": "NP_056199.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2697,
"cds_start": -4,
"cds_end": null,
"cds_length": 8094,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10379,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "ENST00000652901.1",
"protein_id": "ENSP00000499536.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2649,
"cds_start": -4,
"cds_end": null,
"cds_length": 7950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9228,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "n.44-3T>G",
"hgvs_p": null,
"transcript": "ENST00000505998.5",
"protein_id": null,
"transcript_support_level": 5,
"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": 969,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "XM_006714467.3",
"protein_id": "XP_006714530.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2755,
"cds_start": -4,
"cds_end": null,
"cds_length": 8268,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10278,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "XM_006714468.3",
"protein_id": "XP_006714531.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2738,
"cds_start": -4,
"cds_end": null,
"cds_length": 8217,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10227,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "XM_017009329.2",
"protein_id": "XP_016864818.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2649,
"cds_start": -4,
"cds_end": null,
"cds_length": 7950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10319,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"hgvs_c": "c.65-3T>G",
"hgvs_p": null,
"transcript": "XM_011514015.2",
"protein_id": "XP_011512317.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2421,
"cds_start": -4,
"cds_end": null,
"cds_length": 7266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7895,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "NIPBL",
"gene_hgnc_id": 28862,
"dbsnp": "rs727503768",
"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": -0.3400000035762787,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.7279999852180481,
"splice_prediction_selected": "Pathogenic",
"splice_source_selected": "dbscSNV1_RF",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.34,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.849,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.99,
"spliceai_max_prediction": "Pathogenic",
"dbscsnv_ada_score": 0.99065505108356,
"dbscsnv_ada_prediction": "Pathogenic",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 4,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3,PP5",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3",
"PP5"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000282516.13",
"gene_symbol": "NIPBL",
"hgnc_id": 28862,
"effects": [
"splice_region_variant",
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.65-3T>G",
"hgvs_p": null
}
],
"clinvar_disease": "Cornelia de Lange syndrome 1",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Cornelia de Lange syndrome 1",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}