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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: 12-111447506-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=111447506&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 111447506,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000341259.7",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1198G>A",
"hgvs_p": "p.Glu400Lys",
"transcript": "NM_005475.3",
"protein_id": "NP_005466.1",
"transcript_support_level": null,
"aa_start": 400,
"aa_end": null,
"aa_length": 575,
"cds_start": 1198,
"cds_end": null,
"cds_length": 1728,
"cdna_start": 1580,
"cdna_end": null,
"cdna_length": 5431,
"mane_select": "ENST00000341259.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1198G>A",
"hgvs_p": "p.Glu400Lys",
"transcript": "ENST00000341259.7",
"protein_id": "ENSP00000345492.2",
"transcript_support_level": 1,
"aa_start": 400,
"aa_end": null,
"aa_length": 575,
"cds_start": 1198,
"cds_end": null,
"cds_length": 1728,
"cdna_start": 1580,
"cdna_end": null,
"cdna_length": 5431,
"mane_select": "NM_005475.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.592G>A",
"hgvs_p": "p.Glu198Lys",
"transcript": "NM_001291424.1",
"protein_id": "NP_001278353.1",
"transcript_support_level": null,
"aa_start": 198,
"aa_end": null,
"aa_length": 373,
"cds_start": 592,
"cds_end": null,
"cds_length": 1122,
"cdna_start": 632,
"cdna_end": null,
"cdna_length": 4483,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.592G>A",
"hgvs_p": "p.Glu198Lys",
"transcript": "ENST00000538307.1",
"protein_id": "ENSP00000440597.1",
"transcript_support_level": 2,
"aa_start": 198,
"aa_end": null,
"aa_length": 373,
"cds_start": 592,
"cds_end": null,
"cds_length": 1122,
"cdna_start": 632,
"cdna_end": null,
"cdna_length": 2062,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1321G>A",
"hgvs_p": "p.Glu441Lys",
"transcript": "XM_011537719.3",
"protein_id": "XP_011536021.1",
"transcript_support_level": null,
"aa_start": 441,
"aa_end": null,
"aa_length": 616,
"cds_start": 1321,
"cds_end": null,
"cds_length": 1851,
"cdna_start": 1703,
"cdna_end": null,
"cdna_length": 5554,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1321G>A",
"hgvs_p": "p.Glu441Lys",
"transcript": "XM_011537720.4",
"protein_id": "XP_011536022.1",
"transcript_support_level": null,
"aa_start": 441,
"aa_end": null,
"aa_length": 616,
"cds_start": 1321,
"cds_end": null,
"cds_length": 1851,
"cdna_start": 1743,
"cdna_end": null,
"cdna_length": 5594,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1318G>A",
"hgvs_p": "p.Glu440Lys",
"transcript": "XM_005253818.5",
"protein_id": "XP_005253875.1",
"transcript_support_level": null,
"aa_start": 440,
"aa_end": null,
"aa_length": 615,
"cds_start": 1318,
"cds_end": null,
"cds_length": 1848,
"cdna_start": 1700,
"cdna_end": null,
"cdna_length": 5551,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1318G>A",
"hgvs_p": "p.Glu440Lys",
"transcript": "XM_047428025.1",
"protein_id": "XP_047283981.1",
"transcript_support_level": null,
"aa_start": 440,
"aa_end": null,
"aa_length": 615,
"cds_start": 1318,
"cds_end": null,
"cds_length": 1848,
"cdna_start": 1740,
"cdna_end": null,
"cdna_length": 5591,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1201G>A",
"hgvs_p": "p.Glu401Lys",
"transcript": "XM_005253819.5",
"protein_id": "XP_005253876.1",
"transcript_support_level": null,
"aa_start": 401,
"aa_end": null,
"aa_length": 576,
"cds_start": 1201,
"cds_end": null,
"cds_length": 1731,
"cdna_start": 1583,
"cdna_end": null,
"cdna_length": 5434,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.1198G>A",
"hgvs_p": "p.Glu400Lys",
"transcript": "XM_047428026.1",
"protein_id": "XP_047283982.1",
"transcript_support_level": null,
"aa_start": 400,
"aa_end": null,
"aa_length": 575,
"cds_start": 1198,
"cds_end": null,
"cds_length": 1728,
"cdna_start": 1620,
"cdna_end": null,
"cdna_length": 5471,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.400G>A",
"hgvs_p": "p.Glu134Lys",
"transcript": "XM_006719180.5",
"protein_id": "XP_006719243.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 309,
"cds_start": 400,
"cds_end": null,
"cds_length": 930,
"cdna_start": 1658,
"cdna_end": null,
"cdna_length": 5509,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"hgvs_c": "c.397G>A",
"hgvs_p": "p.Glu133Lys",
"transcript": "XM_047428028.1",
"protein_id": "XP_047283984.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 308,
"cds_start": 397,
"cds_end": null,
"cds_length": 927,
"cdna_start": 687,
"cdna_end": null,
"cdna_length": 4538,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "ATXN2",
"gene_hgnc_id": 10555,
"hgvs_c": "n.*171-3319C>T",
"hgvs_p": null,
"transcript": "ENST00000642389.2",
"protein_id": "ENSP00000496055.2",
"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": 4438,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SH2B3",
"gene_hgnc_id": 29605,
"dbsnp": "rs72650673",
"frequency_reference_population": 0.0014439279,
"hom_count_reference_population": 3,
"allele_count_reference_population": 2150,
"gnomad_exomes_af": 0.00150995,
"gnomad_genomes_af": 0.000790444,
"gnomad_exomes_ac": 2042,
"gnomad_genomes_ac": 108,
"gnomad_exomes_homalt": 3,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3876110315322876,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.507,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.7868,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.1,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 9.602,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4,BS1_Supporting,BS2",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4",
"BS1_Supporting",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000341259.7",
"gene_symbol": "SH2B3",
"hgnc_id": 29605,
"effects": [
"missense_variant"
],
"inheritance_mode": "Unknown,AR",
"hgvs_c": "c.1198G>A",
"hgvs_p": "p.Glu400Lys"
},
{
"score": -5,
"benign_score": 5,
"pathogenic_score": 0,
"criteria": [
"BP4",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000642389.2",
"gene_symbol": "ATXN2",
"hgnc_id": 10555,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "n.*171-3319C>T",
"hgvs_p": null
}
],
"clinvar_disease": "Primary familial polycythemia due to EPO receptor mutation,Primary myelofibrosis,Thrombocythemia 1,not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:5",
"phenotype_combined": "not provided|Primary familial polycythemia due to EPO receptor mutation;Thrombocythemia 1;Primary myelofibrosis",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}