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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: 17-18274905-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=18274905&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 18274905,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_004618.5",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2903G>A",
"hgvs_p": "p.Arg968Gln",
"transcript": "NM_004618.5",
"protein_id": "NP_004609.1",
"transcript_support_level": null,
"aa_start": 968,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2903,
"cds_end": null,
"cds_length": 3006,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000321105.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004618.5"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2903G>A",
"hgvs_p": "p.Arg968Gln",
"transcript": "ENST00000321105.10",
"protein_id": "ENSP00000321636.5",
"transcript_support_level": 1,
"aa_start": 968,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2903,
"cds_end": null,
"cds_length": 3006,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_004618.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000321105.10"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2828G>A",
"hgvs_p": "p.Arg943Gln",
"transcript": "ENST00000580095.5",
"protein_id": "ENSP00000462790.1",
"transcript_support_level": 1,
"aa_start": 943,
"aa_end": null,
"aa_length": 975,
"cds_start": 2828,
"cds_end": null,
"cds_length": 2929,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000580095.5"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.3059G>A",
"hgvs_p": "p.Arg1020Gln",
"transcript": "ENST00000924978.1",
"protein_id": "ENSP00000595037.1",
"transcript_support_level": null,
"aa_start": 1020,
"aa_end": null,
"aa_length": 1053,
"cds_start": 3059,
"cds_end": null,
"cds_length": 3162,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924978.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2828G>A",
"hgvs_p": "p.Arg943Gln",
"transcript": "ENST00000924977.1",
"protein_id": "ENSP00000595036.1",
"transcript_support_level": null,
"aa_start": 943,
"aa_end": null,
"aa_length": 976,
"cds_start": 2828,
"cds_end": null,
"cds_length": 2931,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924977.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2789G>A",
"hgvs_p": "p.Arg930Gln",
"transcript": "ENST00000947450.1",
"protein_id": "ENSP00000617509.1",
"transcript_support_level": null,
"aa_start": 930,
"aa_end": null,
"aa_length": 963,
"cds_start": 2789,
"cds_end": null,
"cds_length": 2892,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000947450.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2753G>A",
"hgvs_p": "p.Arg918Gln",
"transcript": "ENST00000924980.1",
"protein_id": "ENSP00000595039.1",
"transcript_support_level": null,
"aa_start": 918,
"aa_end": null,
"aa_length": 951,
"cds_start": 2753,
"cds_end": null,
"cds_length": 2856,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924980.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2618G>A",
"hgvs_p": "p.Arg873Gln",
"transcript": "NM_001320759.2",
"protein_id": "NP_001307688.1",
"transcript_support_level": null,
"aa_start": 873,
"aa_end": null,
"aa_length": 906,
"cds_start": 2618,
"cds_end": null,
"cds_length": 2721,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001320759.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.2099G>A",
"hgvs_p": "p.Arg700Gln",
"transcript": "ENST00000924979.1",
"protein_id": "ENSP00000595038.1",
"transcript_support_level": null,
"aa_start": 700,
"aa_end": null,
"aa_length": 733,
"cds_start": 2099,
"cds_end": null,
"cds_length": 2202,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924979.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.1982G>A",
"hgvs_p": "p.Arg661Gln",
"transcript": "XM_047436633.1",
"protein_id": "XP_047292589.1",
"transcript_support_level": null,
"aa_start": 661,
"aa_end": null,
"aa_length": 694,
"cds_start": 1982,
"cds_end": null,
"cds_length": 2085,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047436633.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.1982G>A",
"hgvs_p": "p.Arg661Gln",
"transcript": "XM_047436634.1",
"protein_id": "XP_047292590.1",
"transcript_support_level": null,
"aa_start": 661,
"aa_end": null,
"aa_length": 694,
"cds_start": 1982,
"cds_end": null,
"cds_length": 2085,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047436634.1"
},
{
"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": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.2258G>A",
"hgvs_p": null,
"transcript": "ENST00000469739.6",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000469739.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.53G>A",
"hgvs_p": null,
"transcript": "ENST00000493648.1",
"protein_id": "ENSP00000465014.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000493648.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.*2559G>A",
"hgvs_p": null,
"transcript": "ENST00000582981.5",
"protein_id": "ENSP00000462378.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000582981.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.*2559G>A",
"hgvs_p": null,
"transcript": "ENST00000584582.5",
"protein_id": "ENSP00000462136.1",
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000584582.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.*2559G>A",
"hgvs_p": null,
"transcript": "ENST00000582981.5",
"protein_id": "ENSP00000462378.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000582981.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "n.*2559G>A",
"hgvs_p": null,
"transcript": "ENST00000584582.5",
"protein_id": "ENSP00000462136.1",
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000584582.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"hgvs_c": "c.-29G>A",
"hgvs_p": null,
"transcript": "ENST00000489131.1",
"protein_id": "ENSP00000465864.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 24,
"cds_start": null,
"cds_end": null,
"cds_length": 75,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000489131.1"
}
],
"gene_symbol": "TOP3A",
"gene_hgnc_id": 11992,
"dbsnp": "rs754772043",
"frequency_reference_population": 0.000101611535,
"hom_count_reference_population": 0,
"allele_count_reference_population": 164,
"gnomad_exomes_af": 0.000106711,
"gnomad_genomes_af": 0.0000525956,
"gnomad_exomes_ac": 156,
"gnomad_genomes_ac": 8,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.07838273048400879,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.037,
"revel_prediction": "Benign",
"alphamissense_score": 0.0795,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.63,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.277,
"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": -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_004618.5",
"gene_symbol": "TOP3A",
"hgnc_id": 11992,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2903G>A",
"hgvs_p": "p.Arg968Gln"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}