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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: 7-100572689-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=100572689&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 100572689,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001348680.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.574C>A",
"hgvs_p": "p.Arg192Ser",
"transcript": "NM_001348680.2",
"protein_id": "NP_001335609.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 297,
"cds_start": 574,
"cds_end": null,
"cds_length": 894,
"cdna_start": 732,
"cdna_end": null,
"cdna_length": 1111,
"mane_select": "ENST00000622764.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.574C>A",
"hgvs_p": "p.Arg192Ser",
"transcript": "ENST00000622764.3",
"protein_id": "ENSP00000481773.2",
"transcript_support_level": 5,
"aa_start": 192,
"aa_end": null,
"aa_length": 297,
"cds_start": 574,
"cds_end": null,
"cds_length": 894,
"cdna_start": 732,
"cdna_end": null,
"cdna_length": 1111,
"mane_select": "NM_001348680.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.553C>A",
"hgvs_p": "p.Arg185Ser",
"transcript": "NM_001168682.3",
"protein_id": "NP_001162153.2",
"transcript_support_level": null,
"aa_start": 185,
"aa_end": null,
"aa_length": 290,
"cds_start": 553,
"cds_end": null,
"cds_length": 873,
"cdna_start": 711,
"cdna_end": null,
"cdna_length": 1090,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.280C>A",
"hgvs_p": "p.Arg94Ser",
"transcript": "NM_001348677.2",
"protein_id": "NP_001335606.1",
"transcript_support_level": null,
"aa_start": 94,
"aa_end": null,
"aa_length": 199,
"cds_start": 280,
"cds_end": null,
"cds_length": 600,
"cdna_start": 928,
"cdna_end": null,
"cdna_length": 1307,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.280C>A",
"hgvs_p": "p.Arg94Ser",
"transcript": "ENST00000538735.5",
"protein_id": "ENSP00000442339.1",
"transcript_support_level": 3,
"aa_start": 94,
"aa_end": null,
"aa_length": 199,
"cds_start": 280,
"cds_end": null,
"cds_length": 600,
"cdna_start": 458,
"cdna_end": null,
"cdna_length": 837,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.280C>A",
"hgvs_p": "p.Arg94Ser",
"transcript": "ENST00000614631.4",
"protein_id": "ENSP00000481351.1",
"transcript_support_level": 2,
"aa_start": 94,
"aa_end": null,
"aa_length": 199,
"cds_start": 280,
"cds_end": null,
"cds_length": 600,
"cdna_start": 636,
"cdna_end": null,
"cdna_length": 987,
"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": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000274272",
"gene_hgnc_id": null,
"hgvs_c": "n.4026C>A",
"hgvs_p": null,
"transcript": "ENST00000485071.2",
"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": 4401,
"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": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "n.378C>A",
"hgvs_p": null,
"transcript": "ENST00000611464.1",
"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": 668,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"dbsnp": "rs1471587814",
"frequency_reference_population": 0.0000036133538,
"hom_count_reference_population": 0,
"allele_count_reference_population": 5,
"gnomad_exomes_af": 0.00000361335,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 5,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.43998193740844727,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.181,
"revel_prediction": "Benign",
"alphamissense_score": 0.6929,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.2,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.14,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001348680.2",
"gene_symbol": "SAP25",
"hgnc_id": 41908,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.574C>A",
"hgvs_p": "p.Arg192Ser"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000485071.2",
"gene_symbol": "ENSG00000274272",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.4026C>A",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}