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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: 18-46680100-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=46680100&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "18",
"pos": 46680100,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001307986.2",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1073T>A",
"hgvs_p": "p.Leu358Gln",
"transcript": "NM_013305.6",
"protein_id": "NP_037437.2",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 376,
"cds_start": 1073,
"cds_end": null,
"cds_length": 1131,
"cdna_start": 1618,
"cdna_end": null,
"cdna_length": 13897,
"mane_select": "ENST00000315087.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_013305.6"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1073T>A",
"hgvs_p": "p.Leu358Gln",
"transcript": "ENST00000315087.12",
"protein_id": "ENSP00000321343.6",
"transcript_support_level": 1,
"aa_start": 358,
"aa_end": null,
"aa_length": 376,
"cds_start": 1073,
"cds_end": null,
"cds_length": 1131,
"cdna_start": 1618,
"cdna_end": null,
"cdna_length": 13897,
"mane_select": "NM_013305.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000315087.12"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1181T>A",
"hgvs_p": "p.Leu394Gln",
"transcript": "NM_001307986.2",
"protein_id": "NP_001294915.1",
"transcript_support_level": null,
"aa_start": 394,
"aa_end": null,
"aa_length": 412,
"cds_start": 1181,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 1726,
"cdna_end": null,
"cdna_length": 14005,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001307986.2"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1181T>A",
"hgvs_p": "p.Leu394Gln",
"transcript": "ENST00000538168.5",
"protein_id": "ENSP00000445492.1",
"transcript_support_level": 2,
"aa_start": 394,
"aa_end": null,
"aa_length": 412,
"cds_start": 1181,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 1482,
"cdna_end": null,
"cdna_length": 13761,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000538168.5"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1166T>A",
"hgvs_p": "p.Leu389Gln",
"transcript": "ENST00000911623.1",
"protein_id": "ENSP00000581682.1",
"transcript_support_level": null,
"aa_start": 389,
"aa_end": null,
"aa_length": 407,
"cds_start": 1166,
"cds_end": null,
"cds_length": 1224,
"cdna_start": 1496,
"cdna_end": null,
"cdna_length": 2472,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911623.1"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1088T>A",
"hgvs_p": "p.Leu363Gln",
"transcript": "ENST00000906003.1",
"protein_id": "ENSP00000576062.1",
"transcript_support_level": null,
"aa_start": 363,
"aa_end": null,
"aa_length": 381,
"cds_start": 1088,
"cds_end": null,
"cds_length": 1146,
"cdna_start": 1393,
"cdna_end": null,
"cdna_length": 2251,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000906003.1"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.1058T>A",
"hgvs_p": "p.Leu353Gln",
"transcript": "ENST00000951068.1",
"protein_id": "ENSP00000621127.1",
"transcript_support_level": null,
"aa_start": 353,
"aa_end": null,
"aa_length": 371,
"cds_start": 1058,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1597,
"cdna_end": null,
"cdna_length": 2454,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951068.1"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.980T>A",
"hgvs_p": "p.Leu327Gln",
"transcript": "NM_001307987.2",
"protein_id": "NP_001294916.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 345,
"cds_start": 980,
"cds_end": null,
"cds_length": 1038,
"cdna_start": 1525,
"cdna_end": null,
"cdna_length": 13804,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001307987.2"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.980T>A",
"hgvs_p": "p.Leu327Gln",
"transcript": "ENST00000536490.1",
"protein_id": "ENSP00000443683.1",
"transcript_support_level": 2,
"aa_start": 327,
"aa_end": null,
"aa_length": 345,
"cds_start": 980,
"cds_end": null,
"cds_length": 1038,
"cdna_start": 1282,
"cdna_end": null,
"cdna_length": 1499,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000536490.1"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.728T>A",
"hgvs_p": "p.Leu243Gln",
"transcript": "ENST00000906002.1",
"protein_id": "ENSP00000576061.1",
"transcript_support_level": null,
"aa_start": 243,
"aa_end": null,
"aa_length": 261,
"cds_start": 728,
"cds_end": null,
"cds_length": 786,
"cdna_start": 1267,
"cdna_end": null,
"cdna_length": 2125,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000906002.1"
},
{
"aa_ref": "L",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "c.635T>A",
"hgvs_p": "p.Leu212Gln",
"transcript": "ENST00000906001.1",
"protein_id": "ENSP00000576060.1",
"transcript_support_level": null,
"aa_start": 212,
"aa_end": null,
"aa_length": 230,
"cds_start": 635,
"cds_end": null,
"cds_length": 693,
"cdna_start": 1180,
"cdna_end": null,
"cdna_length": 2051,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000906001.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"hgvs_c": "n.1237T>A",
"hgvs_p": null,
"transcript": "ENST00000590497.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2094,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000590497.5"
}
],
"gene_symbol": "ST8SIA5",
"gene_hgnc_id": 17827,
"dbsnp": "rs1568246567",
"frequency_reference_population": 6.8409935e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84099e-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": 0.5215804576873779,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.27,
"revel_prediction": "Benign",
"alphamissense_score": 0.9116,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.3,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 9.219,
"phylop100way_prediction": "Pathogenic",
"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_001307986.2",
"gene_symbol": "ST8SIA5",
"hgnc_id": 17827,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1181T>A",
"hgvs_p": "p.Leu394Gln"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}