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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: 3-10466811-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=10466811&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 10466811,
"ref": "T",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000360273.7",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "NM_001001331.4",
"protein_id": "NP_001001331.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1243,
"cds_start": -4,
"cds_end": null,
"cds_length": 3732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8964,
"mane_select": "ENST00000360273.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "ENST00000360273.7",
"protein_id": "ENSP00000353414.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1243,
"cds_start": -4,
"cds_end": null,
"cds_length": 3732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8964,
"mane_select": "NM_001001331.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "ENST00000397077.6",
"protein_id": "ENSP00000380267.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1198,
"cds_start": -4,
"cds_end": null,
"cds_length": 3597,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8779,
"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": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "n.121-16949A>G",
"hgvs_p": null,
"transcript": "ENST00000480680.2",
"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": 1739,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "NM_001438646.1",
"protein_id": "NP_001425575.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1212,
"cds_start": -4,
"cds_end": null,
"cds_length": 3639,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8871,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "NM_001353564.1",
"protein_id": "NP_001340493.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1198,
"cds_start": -4,
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"cds_length": 3597,
"cdna_start": null,
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"cdna_length": 8847,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "NM_001438036.1",
"protein_id": "NP_001424965.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1198,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 9049,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "NM_001683.5",
"protein_id": "NP_001674.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1198,
"cds_start": -4,
"cds_end": null,
"cds_length": 3597,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8829,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "ENST00000646379.1",
"protein_id": "ENSP00000494381.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1198,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 4955,
"mane_select": null,
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"feature": null
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 1,
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"gene_symbol": "ATP2B2",
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"hgvs_c": "c.-319-16949A>G",
"hgvs_p": null,
"transcript": "ENST00000643662.1",
"protein_id": "ENSP00000495924.1",
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"cds_start": -4,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 1,
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"gene_symbol": "ATP2B2",
"gene_hgnc_id": 815,
"hgvs_c": "c.-319-16949A>G",
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"transcript": "NM_001363862.1",
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},
{
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],
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"gene_symbol": "ATP2B2",
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},
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],
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"gene_symbol": "ATP2B2",
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"hgvs_c": "c.-319-16949A>G",
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},
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],
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"gene_symbol": "ATP2B2",
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],
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},
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],
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},
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],
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"gene_symbol": "ATP2B2",
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"hgvs_c": "c.-319-16949A>G",
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"transcript": "XM_017006481.3",
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],
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],
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"gene_symbol": "ATP2B2",
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},
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"consequences": [
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],
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"gene_symbol": "ATP2B2",
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},
{
"aa_ref": null,
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],
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}
],
"gene_symbol": "ATP2B2",
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"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.597106,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 90852,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 27866,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8600000143051147,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
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"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.86,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.093,
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000360273.7",
"gene_symbol": "ATP2B2",
"hgnc_id": 815,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.-319-16949A>G",
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}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}