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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: 17-10638363-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=10638363&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 10638363,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000583535.6",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys",
"transcript": "NM_002470.4",
"protein_id": "NP_002461.2",
"transcript_support_level": null,
"aa_start": 1137,
"aa_end": null,
"aa_length": 1940,
"cds_start": 3409,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 3497,
"cdna_end": null,
"cdna_length": 6032,
"mane_select": "ENST00000583535.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys",
"transcript": "ENST00000583535.6",
"protein_id": "ENSP00000464317.1",
"transcript_support_level": 5,
"aa_start": 1137,
"aa_end": null,
"aa_length": 1940,
"cds_start": 3409,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 3497,
"cdna_end": null,
"cdna_length": 6032,
"mane_select": "NM_002470.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys",
"transcript": "XM_011523870.4",
"protein_id": "XP_011522172.1",
"transcript_support_level": null,
"aa_start": 1137,
"aa_end": null,
"aa_length": 1940,
"cds_start": 3409,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 3624,
"cdna_end": null,
"cdna_length": 6159,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys",
"transcript": "XM_011523871.3",
"protein_id": "XP_011522173.1",
"transcript_support_level": null,
"aa_start": 1137,
"aa_end": null,
"aa_length": 1940,
"cds_start": 3409,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 3550,
"cdna_end": null,
"cdna_length": 6085,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys",
"transcript": "XM_047436127.1",
"protein_id": "XP_047292083.1",
"transcript_support_level": null,
"aa_start": 1137,
"aa_end": null,
"aa_length": 1940,
"cds_start": 3409,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 6720,
"cdna_end": null,
"cdna_length": 9255,
"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": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "MYHAS",
"gene_hgnc_id": 50609,
"hgvs_c": "n.705+24486G>A",
"hgvs_p": null,
"transcript": "ENST00000579914.2",
"protein_id": null,
"transcript_support_level": 4,
"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": 1006,
"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": 9,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYHAS",
"gene_hgnc_id": 50609,
"hgvs_c": "n.1041+24486G>A",
"hgvs_p": null,
"transcript": "ENST00000584139.2",
"protein_id": null,
"transcript_support_level": 3,
"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": 1460,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MYH3",
"gene_hgnc_id": 7573,
"dbsnp": "rs12941197",
"frequency_reference_population": 0.0035909344,
"hom_count_reference_population": 17,
"allele_count_reference_population": 5774,
"gnomad_exomes_af": 0.00371941,
"gnomad_genomes_af": 0.00236088,
"gnomad_exomes_ac": 5415,
"gnomad_genomes_ac": 359,
"gnomad_exomes_homalt": 15,
"gnomad_genomes_homalt": 2,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.014895111322402954,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.718,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.3406,
"alphamissense_prediction": "Uncertain_significance",
"bayesdelnoaf_score": 0.31,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 2.227,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS2",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000583535.6",
"gene_symbol": "MYH3",
"hgnc_id": 7573,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.3409C>T",
"hgvs_p": "p.Arg1137Cys"
},
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000584139.2",
"gene_symbol": "MYHAS",
"hgnc_id": 50609,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.1041+24486G>A",
"hgvs_p": null
}
],
"clinvar_disease": " and spondylocarpotarsal fusion syndrome 1A, and variable skeletal fusions syndrome 1B, distal, pterygia, type 2B3,Arthrogryposis,Contractures,Distal arthrogryposis type 2B1,Freeman-Sheldon syndrome,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:4 B:3",
"phenotype_combined": "not specified|Freeman-Sheldon syndrome|Distal arthrogryposis type 2B1|Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A;Contractures, pterygia, and variable skeletal fusions syndrome 1B;Freeman-Sheldon syndrome;Arthrogryposis, distal, type 2B3|not provided",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}