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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: 17-78358808-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=78358808&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 78358808,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000330871.3",
"consequences": [
{
"aa_ref": "Q",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"hgvs_c": "c.288G>C",
"hgvs_p": "p.Gln96His",
"transcript": "NM_003955.5",
"protein_id": "NP_003946.3",
"transcript_support_level": null,
"aa_start": 96,
"aa_end": null,
"aa_length": 225,
"cds_start": 288,
"cds_end": null,
"cds_length": 678,
"cdna_start": 704,
"cdna_end": null,
"cdna_length": 2734,
"mane_select": "ENST00000330871.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"hgvs_c": "c.288G>C",
"hgvs_p": "p.Gln96His",
"transcript": "ENST00000330871.3",
"protein_id": "ENSP00000330341.2",
"transcript_support_level": 1,
"aa_start": 96,
"aa_end": null,
"aa_length": 225,
"cds_start": 288,
"cds_end": null,
"cds_length": 678,
"cdna_start": 704,
"cdna_end": null,
"cdna_length": 2734,
"mane_select": "NM_003955.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"hgvs_c": "c.288G>C",
"hgvs_p": "p.Gln96His",
"transcript": "NM_001378932.1",
"protein_id": "NP_001365861.1",
"transcript_support_level": null,
"aa_start": 96,
"aa_end": null,
"aa_length": 225,
"cds_start": 288,
"cds_end": null,
"cds_length": 678,
"cdna_start": 399,
"cdna_end": null,
"cdna_length": 2429,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"hgvs_c": "c.288G>C",
"hgvs_p": "p.Gln96His",
"transcript": "NM_001378933.1",
"protein_id": "NP_001365862.1",
"transcript_support_level": null,
"aa_start": 96,
"aa_end": null,
"aa_length": 225,
"cds_start": 288,
"cds_end": null,
"cds_length": 678,
"cdna_start": 446,
"cdna_end": null,
"cdna_length": 2476,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "SOCS3-DT",
"gene_hgnc_id": 52799,
"hgvs_c": "n.422+598C>G",
"hgvs_p": null,
"transcript": "ENST00000794159.1",
"protein_id": null,
"transcript_support_level": null,
"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": 932,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SOCS3-DT",
"gene_hgnc_id": 52799,
"hgvs_c": "n.302+211C>G",
"hgvs_p": null,
"transcript": "ENST00000794160.1",
"protein_id": null,
"transcript_support_level": null,
"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": 879,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SOCS3-DT",
"gene_hgnc_id": 52799,
"hgvs_c": "n.265+211C>G",
"hgvs_p": null,
"transcript": "ENST00000794161.1",
"protein_id": null,
"transcript_support_level": null,
"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": 773,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"hgvs_c": "c.*241G>C",
"hgvs_p": null,
"transcript": "ENST00000587578.1",
"protein_id": "ENSP00000464727.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 14,
"cds_start": -4,
"cds_end": null,
"cds_length": 47,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SOCS3",
"gene_hgnc_id": 19391,
"dbsnp": "rs12059",
"frequency_reference_population": 6.8449833e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84498e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.4286005198955536,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.297,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.5312,
"alphamissense_prediction": "Uncertain_significance",
"bayesdelnoaf_score": -0.17,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.19,
"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": "ENST00000330871.3",
"gene_symbol": "SOCS3",
"hgnc_id": 19391,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.288G>C",
"hgvs_p": "p.Gln96His"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000794159.1",
"gene_symbol": "SOCS3-DT",
"hgnc_id": 52799,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.422+598C>G",
"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
}