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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: X-101391786-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=101391786&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 101391786,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_021029.6",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "NM_021029.6",
"protein_id": "NP_066357.3",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 106,
"cds_start": 141,
"cds_end": null,
"cds_length": 321,
"cdna_start": 174,
"cdna_end": null,
"cdna_length": 761,
"mane_select": "ENST00000553110.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "ENST00000553110.8",
"protein_id": "ENSP00000446503.2",
"transcript_support_level": 1,
"aa_start": 47,
"aa_end": null,
"aa_length": 106,
"cds_start": 141,
"cds_end": null,
"cds_length": 321,
"cdna_start": 174,
"cdna_end": null,
"cdna_length": 761,
"mane_select": "NM_021029.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.249C>T",
"hgvs_p": "p.Gly83Gly",
"transcript": "ENST00000427805.6",
"protein_id": "ENSP00000404375.2",
"transcript_support_level": 1,
"aa_start": 83,
"aa_end": null,
"aa_length": 142,
"cds_start": 249,
"cds_end": null,
"cds_length": 429,
"cdna_start": 361,
"cdna_end": null,
"cdna_length": 910,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.249C>T",
"hgvs_p": "p.Gly83Gly",
"transcript": "ENST00000614077.4",
"protein_id": "ENSP00000483017.1",
"transcript_support_level": 1,
"aa_start": 83,
"aa_end": null,
"aa_length": 142,
"cds_start": 249,
"cds_end": null,
"cds_length": 429,
"cdna_start": 295,
"cdna_end": null,
"cdna_length": 881,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A-HNRNPH2",
"gene_hgnc_id": 48349,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "ENST00000409170.3",
"protein_id": "ENSP00000386655.4",
"transcript_support_level": 4,
"aa_start": 47,
"aa_end": null,
"aa_length": 118,
"cds_start": 141,
"cds_end": null,
"cds_length": 357,
"cdna_start": 173,
"cdna_end": null,
"cdna_length": 562,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "n.483C>T",
"hgvs_p": null,
"transcript": "ENST00000465744.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 710,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A-HNRNPH2",
"gene_hgnc_id": 48349,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "NM_001199973.2",
"protein_id": "NP_001186902.2",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 118,
"cds_start": 141,
"cds_end": null,
"cds_length": 357,
"cdna_start": 174,
"cdna_end": null,
"cdna_length": 2531,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "ENST00000392994.7",
"protein_id": "ENSP00000397659.3",
"transcript_support_level": 2,
"aa_start": 47,
"aa_end": null,
"aa_length": 112,
"cds_start": 141,
"cds_end": null,
"cds_length": 339,
"cdna_start": 196,
"cdna_end": null,
"cdna_length": 691,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A-HNRNPH2",
"gene_hgnc_id": 48349,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "NM_001199974.2",
"protein_id": "NP_001186903.2",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 77,
"cds_start": 141,
"cds_end": null,
"cds_length": 234,
"cdna_start": 174,
"cdna_end": null,
"cdna_length": 2408,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A-HNRNPH2",
"gene_hgnc_id": 48349,
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly",
"transcript": "ENST00000409338.5",
"protein_id": "ENSP00000386974.2",
"transcript_support_level": 4,
"aa_start": 47,
"aa_end": null,
"aa_length": 77,
"cds_start": 141,
"cds_end": null,
"cds_length": 234,
"cdna_start": 174,
"cdna_end": null,
"cdna_length": 572,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "n.141C>T",
"hgvs_p": null,
"transcript": "ENST00000372849.8",
"protein_id": "ENSP00000361940.5",
"transcript_support_level": 5,
"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": 433,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "n.174C>T",
"hgvs_p": null,
"transcript": "ENST00000465340.5",
"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": 2240,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "n.364C>T",
"hgvs_p": null,
"transcript": "ENST00000491851.5",
"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": 547,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"hgvs_c": "c.-103C>T",
"hgvs_p": null,
"transcript": "ENST00000471855.1",
"protein_id": "ENSP00000473451.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 25,
"cds_start": -4,
"cds_end": null,
"cds_length": 78,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 399,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "RPL36A",
"gene_hgnc_id": 10359,
"dbsnp": "rs3027595",
"frequency_reference_population": 0.00634897,
"hom_count_reference_population": 2511,
"allele_count_reference_population": 7674,
"gnomad_exomes_af": 0.0065677,
"gnomad_genomes_af": 0.0042033,
"gnomad_exomes_ac": 7204,
"gnomad_genomes_ac": 470,
"gnomad_exomes_homalt": 16,
"gnomad_genomes_homalt": 2,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.39399999380111694,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "REVEL",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.394,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.41,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.063,
"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": -13,
"acmg_classification": "Benign",
"acmg_criteria": "BP6_Very_Strong,BP7,BS2",
"acmg_by_gene": [
{
"score": -13,
"benign_score": 13,
"pathogenic_score": 0,
"criteria": [
"BP6_Very_Strong",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_021029.6",
"gene_symbol": "RPL36A",
"hgnc_id": 10359,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly"
},
{
"score": -13,
"benign_score": 13,
"pathogenic_score": 0,
"criteria": [
"BP6_Very_Strong",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000409170.3",
"gene_symbol": "RPL36A-HNRNPH2",
"hgnc_id": 48349,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.141C>T",
"hgvs_p": "p.Gly47Gly"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}