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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: 16-3731337-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=3731337&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM1",
"PM2",
"PP3_Moderate"
],
"effects": [
"missense_variant"
],
"gene_symbol": "CREBBP",
"hgnc_id": 2348,
"hgvs_c": "c.5027G>C",
"hgvs_p": "p.Trp1676Ser",
"inheritance_mode": "AD",
"pathogenic_score": 6,
"score": 6,
"transcript": "NM_004380.3",
"verdict": "Likely_pathogenic"
}
],
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PM1,PM2,PP3_Moderate",
"acmg_score": 6,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": 0.9692,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.27,
"chr": "16",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.8653749227523804,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2442,
"aa_ref": "W",
"aa_start": 1676,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10790,
"cdna_start": 5824,
"cds_end": null,
"cds_length": 7329,
"cds_start": 5027,
"consequences": [
"missense_variant"
],
"exon_count": 31,
"exon_rank": 30,
"exon_rank_end": null,
"feature": "NM_004380.3",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.5027G>C",
"hgvs_p": "p.Trp1676Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000262367.10",
"protein_coding": true,
"protein_id": "NP_004371.2",
"strand": false,
"transcript": "NM_004380.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2442,
"aa_ref": "W",
"aa_start": 1676,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 10790,
"cdna_start": 5824,
"cds_end": null,
"cds_length": 7329,
"cds_start": 5027,
"consequences": [
"missense_variant"
],
"exon_count": 31,
"exon_rank": 30,
"exon_rank_end": null,
"feature": "ENST00000262367.10",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.5027G>C",
"hgvs_p": "p.Trp1676Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_004380.3",
"protein_coding": true,
"protein_id": "ENSP00000262367.5",
"strand": false,
"transcript": "ENST00000262367.10",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2404,
"aa_ref": "W",
"aa_start": 1638,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7598,
"cdna_start": 5117,
"cds_end": null,
"cds_length": 7215,
"cds_start": 4913,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "ENST00000382070.7",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4913G>C",
"hgvs_p": "p.Trp1638Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000371502.3",
"strand": false,
"transcript": "ENST00000382070.7",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2404,
"aa_ref": "W",
"aa_start": 1638,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10083,
"cdna_start": 5117,
"cds_end": null,
"cds_length": 7215,
"cds_start": 4913,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "NM_001079846.1",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4913G>C",
"hgvs_p": "p.Trp1638Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001073315.1",
"strand": false,
"transcript": "NM_001079846.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2440,
"aa_ref": "W",
"aa_start": 1674,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10784,
"cdna_start": 5818,
"cds_end": null,
"cds_length": 7323,
"cds_start": 5021,
"consequences": [
"missense_variant"
],
"exon_count": 31,
"exon_rank": 30,
"exon_rank_end": null,
"feature": "XM_017022944.2",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.5021G>C",
"hgvs_p": "p.Trp1674Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016878433.1",
"strand": false,
"transcript": "XM_017022944.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2427,
"aa_ref": "W",
"aa_start": 1661,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10745,
"cdna_start": 5779,
"cds_end": null,
"cds_length": 7284,
"cds_start": 4982,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "XM_005255124.5",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4982G>C",
"hgvs_p": "p.Trp1661Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005255181.1",
"strand": false,
"transcript": "XM_005255124.5",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2425,
"aa_ref": "W",
"aa_start": 1659,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10739,
"cdna_start": 5773,
"cds_end": null,
"cds_length": 7278,
"cds_start": 4976,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "XM_047433624.1",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4976G>C",
"hgvs_p": "p.Trp1659Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047289580.1",
"strand": false,
"transcript": "XM_047433624.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2389,
"aa_ref": "W",
"aa_start": 1623,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10631,
"cdna_start": 5665,
"cds_end": null,
"cds_length": 7170,
"cds_start": 4868,
"consequences": [
"missense_variant"
],
"exon_count": 29,
"exon_rank": 28,
"exon_rank_end": null,
"feature": "XM_047433625.1",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4868G>C",
"hgvs_p": "p.Trp1623Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047289581.1",
"strand": false,
"transcript": "XM_047433625.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2355,
"aa_ref": "W",
"aa_start": 1589,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10529,
"cdna_start": 5563,
"cds_end": null,
"cds_length": 7068,
"cds_start": 4766,
"consequences": [
"missense_variant"
],
"exon_count": 29,
"exon_rank": 28,
"exon_rank_end": null,
"feature": "XM_006720848.4",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4766G>C",
"hgvs_p": "p.Trp1589Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006720911.1",
"strand": false,
"transcript": "XM_006720848.4",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2303,
"aa_ref": "W",
"aa_start": 1537,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10373,
"cdna_start": 5407,
"cds_end": null,
"cds_length": 6912,
"cds_start": 4610,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "XM_005255125.5",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4610G>C",
"hgvs_p": "p.Trp1537Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005255182.1",
"strand": false,
"transcript": "XM_005255125.5",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 2191,
"aa_ref": "W",
"aa_start": 1425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10713,
"cdna_start": 5747,
"cds_end": null,
"cds_length": 6576,
"cds_start": 4274,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 29,
"exon_rank_end": null,
"feature": "XM_011522381.3",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.4274G>C",
"hgvs_p": "p.Trp1425Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011520683.1",
"strand": false,
"transcript": "XM_011522381.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 31,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 100,
"cdna_start": null,
"cds_end": null,
"cds_length": 98,
"cds_start": null,
"consequences": [
"upstream_gene_variant"
],
"exon_count": 2,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000637492.1",
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"hgvs_c": "c.-89G>C",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000490244.1",
"strand": true,
"transcript": "ENST00000637492.1",
"transcript_support_level": 5
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs797045495",
"effect": "missense_variant",
"frequency_reference_population": null,
"gene_hgnc_id": 2348,
"gene_symbol": "CREBBP",
"gnomad_exomes_ac": null,
"gnomad_exomes_af": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_ac": null,
"gnomad_genomes_af": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": null,
"phenotype_combined": null,
"phylop100way_prediction": "Uncertain_significance",
"phylop100way_score": 4.927,
"pos": 3731337,
"ref": "C",
"revel_prediction": "Pathogenic",
"revel_score": 0.723,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_004380.3"
}
]
}