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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: 7-104161085-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=104161085&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 104161085,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_002553.4",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1136A>G",
"hgvs_p": "p.Asn379Ser",
"transcript": "NM_002553.4",
"protein_id": "NP_002544.1",
"transcript_support_level": null,
"aa_start": 379,
"aa_end": null,
"aa_length": 435,
"cds_start": 1136,
"cds_end": null,
"cds_length": 1308,
"cdna_start": 1245,
"cdna_end": null,
"cdna_length": 1924,
"mane_select": "ENST00000297431.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002553.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1136A>G",
"hgvs_p": "p.Asn379Ser",
"transcript": "ENST00000297431.9",
"protein_id": "ENSP00000297431.4",
"transcript_support_level": 1,
"aa_start": 379,
"aa_end": null,
"aa_length": 435,
"cds_start": 1136,
"cds_end": null,
"cds_length": 1308,
"cdna_start": 1245,
"cdna_end": null,
"cdna_length": 1924,
"mane_select": "NM_002553.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000297431.9"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1229A>G",
"hgvs_p": "p.Asn410Ser",
"transcript": "ENST00000938620.1",
"protein_id": "ENSP00000608679.1",
"transcript_support_level": null,
"aa_start": 410,
"aa_end": null,
"aa_length": 466,
"cds_start": 1229,
"cds_end": null,
"cds_length": 1401,
"cdna_start": 1338,
"cdna_end": null,
"cdna_length": 2015,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938620.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1217A>G",
"hgvs_p": "p.Asn406Ser",
"transcript": "ENST00000884268.1",
"protein_id": "ENSP00000554327.1",
"transcript_support_level": null,
"aa_start": 406,
"aa_end": null,
"aa_length": 462,
"cds_start": 1217,
"cds_end": null,
"cds_length": 1389,
"cdna_start": 1334,
"cdna_end": null,
"cdna_length": 2011,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884268.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1145A>G",
"hgvs_p": "p.Asn382Ser",
"transcript": "ENST00000953176.1",
"protein_id": "ENSP00000623235.1",
"transcript_support_level": null,
"aa_start": 382,
"aa_end": null,
"aa_length": 438,
"cds_start": 1145,
"cds_end": null,
"cds_length": 1317,
"cdna_start": 1253,
"cdna_end": null,
"cdna_length": 1930,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953176.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1088A>G",
"hgvs_p": "p.Asn363Ser",
"transcript": "ENST00000938616.1",
"protein_id": "ENSP00000608675.1",
"transcript_support_level": null,
"aa_start": 363,
"aa_end": null,
"aa_length": 419,
"cds_start": 1088,
"cds_end": null,
"cds_length": 1260,
"cdna_start": 1208,
"cdna_end": null,
"cdna_length": 1887,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938616.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1088A>G",
"hgvs_p": "p.Asn363Ser",
"transcript": "ENST00000953177.1",
"protein_id": "ENSP00000623236.1",
"transcript_support_level": null,
"aa_start": 363,
"aa_end": null,
"aa_length": 419,
"cds_start": 1088,
"cds_end": null,
"cds_length": 1260,
"cdna_start": 1192,
"cdna_end": null,
"cdna_length": 1862,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953177.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1052A>G",
"hgvs_p": "p.Asn351Ser",
"transcript": "ENST00000884267.1",
"protein_id": "ENSP00000554326.1",
"transcript_support_level": null,
"aa_start": 351,
"aa_end": null,
"aa_length": 407,
"cds_start": 1052,
"cds_end": null,
"cds_length": 1224,
"cdna_start": 1171,
"cdna_end": null,
"cdna_length": 1848,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884267.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1043A>G",
"hgvs_p": "p.Asn348Ser",
"transcript": "ENST00000884266.1",
"protein_id": "ENSP00000554325.1",
"transcript_support_level": null,
"aa_start": 348,
"aa_end": null,
"aa_length": 404,
"cds_start": 1043,
"cds_end": null,
"cds_length": 1215,
"cdna_start": 1162,
"cdna_end": null,
"cdna_length": 1841,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884266.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.935A>G",
"hgvs_p": "p.Asn312Ser",
"transcript": "ENST00000938619.1",
"protein_id": "ENSP00000608678.1",
"transcript_support_level": null,
"aa_start": 312,
"aa_end": null,
"aa_length": 368,
"cds_start": 935,
"cds_end": null,
"cds_length": 1107,
"cdna_start": 1044,
"cdna_end": null,
"cdna_length": 1723,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938619.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.830A>G",
"hgvs_p": "p.Asn277Ser",
"transcript": "ENST00000938617.1",
"protein_id": "ENSP00000608676.1",
"transcript_support_level": null,
"aa_start": 277,
"aa_end": null,
"aa_length": 333,
"cds_start": 830,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 949,
"cdna_end": null,
"cdna_length": 1628,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938617.1"
},
{
"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": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.1038+4150A>G",
"hgvs_p": null,
"transcript": "ENST00000953178.1",
"protein_id": "ENSP00000623237.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 398,
"cds_start": null,
"cds_end": null,
"cds_length": 1197,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1798,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953178.1"
},
{
"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": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.990+5687A>G",
"hgvs_p": null,
"transcript": "ENST00000953179.1",
"protein_id": "ENSP00000623238.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 382,
"cds_start": null,
"cds_end": null,
"cds_length": 1149,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1743,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000953179.1"
},
{
"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": 8,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "c.685-24192A>G",
"hgvs_p": null,
"transcript": "ENST00000938618.1",
"protein_id": "ENSP00000608677.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 280,
"cds_start": null,
"cds_end": null,
"cds_length": 843,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1460,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938618.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "n.*1069A>G",
"hgvs_p": null,
"transcript": "ENST00000422497.5",
"protein_id": "ENSP00000393208.1",
"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": 2043,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000422497.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"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": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "n.598A>G",
"hgvs_p": null,
"transcript": "ENST00000477223.1",
"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": 780,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000477223.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"hgvs_c": "n.*1069A>G",
"hgvs_p": null,
"transcript": "ENST00000422497.5",
"protein_id": "ENSP00000393208.1",
"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": 2043,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000422497.5"
}
],
"gene_symbol": "ORC5",
"gene_hgnc_id": 8491,
"dbsnp": "rs200169609",
"frequency_reference_population": 0.00019914126,
"hom_count_reference_population": 0,
"allele_count_reference_population": 310,
"gnomad_exomes_af": 0.000209315,
"gnomad_genomes_af": 0.000105191,
"gnomad_exomes_ac": 294,
"gnomad_genomes_ac": 16,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.19495359063148499,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.1,
"revel_prediction": "Benign",
"alphamissense_score": 0.0536,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.65,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.45,
"phylop100way_prediction": "Uncertain_significance",
"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": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_002553.4",
"gene_symbol": "ORC5",
"hgnc_id": 8491,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1136A>G",
"hgvs_p": "p.Asn379Ser"
}
],
"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
}