← Back to variant description
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: 12-56418000-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=56418000&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 56418000,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_003920.5",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3463G>A",
"hgvs_p": "p.Ala1155Thr",
"transcript": "NM_003920.5",
"protein_id": "NP_003911.2",
"transcript_support_level": null,
"aa_start": 1155,
"aa_end": null,
"aa_length": 1208,
"cds_start": 3463,
"cds_end": null,
"cds_length": 3627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000553532.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003920.5"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3463G>A",
"hgvs_p": "p.Ala1155Thr",
"transcript": "ENST00000553532.6",
"protein_id": "ENSP00000450607.1",
"transcript_support_level": 1,
"aa_start": 1155,
"aa_end": null,
"aa_length": 1208,
"cds_start": 3463,
"cds_end": null,
"cds_length": 3627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003920.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000553532.6"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3484G>A",
"hgvs_p": "p.Ala1162Thr",
"transcript": "ENST00000865172.1",
"protein_id": "ENSP00000535231.1",
"transcript_support_level": null,
"aa_start": 1162,
"aa_end": null,
"aa_length": 1215,
"cds_start": 3484,
"cds_end": null,
"cds_length": 3648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865172.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3484G>A",
"hgvs_p": "p.Ala1162Thr",
"transcript": "ENST00000927926.1",
"protein_id": "ENSP00000597985.1",
"transcript_support_level": null,
"aa_start": 1162,
"aa_end": null,
"aa_length": 1215,
"cds_start": 3484,
"cds_end": null,
"cds_length": 3648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927926.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3475G>A",
"hgvs_p": "p.Ala1159Thr",
"transcript": "ENST00000865170.1",
"protein_id": "ENSP00000535229.1",
"transcript_support_level": null,
"aa_start": 1159,
"aa_end": null,
"aa_length": 1212,
"cds_start": 3475,
"cds_end": null,
"cds_length": 3639,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865170.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3472G>A",
"hgvs_p": "p.Ala1158Thr",
"transcript": "ENST00000927924.1",
"protein_id": "ENSP00000597983.1",
"transcript_support_level": null,
"aa_start": 1158,
"aa_end": null,
"aa_length": 1211,
"cds_start": 3472,
"cds_end": null,
"cds_length": 3636,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927924.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3463G>A",
"hgvs_p": "p.Ala1155Thr",
"transcript": "ENST00000865173.1",
"protein_id": "ENSP00000535232.1",
"transcript_support_level": null,
"aa_start": 1155,
"aa_end": null,
"aa_length": 1208,
"cds_start": 3463,
"cds_end": null,
"cds_length": 3627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865173.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3463G>A",
"hgvs_p": "p.Ala1155Thr",
"transcript": "ENST00000971076.1",
"protein_id": "ENSP00000641135.1",
"transcript_support_level": null,
"aa_start": 1155,
"aa_end": null,
"aa_length": 1208,
"cds_start": 3463,
"cds_end": null,
"cds_length": 3627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971076.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3460G>A",
"hgvs_p": "p.Ala1154Thr",
"transcript": "NM_001330295.2",
"protein_id": "NP_001317224.1",
"transcript_support_level": null,
"aa_start": 1154,
"aa_end": null,
"aa_length": 1207,
"cds_start": 3460,
"cds_end": null,
"cds_length": 3624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001330295.2"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3460G>A",
"hgvs_p": "p.Ala1154Thr",
"transcript": "ENST00000229201.4",
"protein_id": "ENSP00000229201.4",
"transcript_support_level": 5,
"aa_start": 1154,
"aa_end": null,
"aa_length": 1207,
"cds_start": 3460,
"cds_end": null,
"cds_length": 3624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000229201.4"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3457G>A",
"hgvs_p": "p.Ala1153Thr",
"transcript": "ENST00000927921.1",
"protein_id": "ENSP00000597980.1",
"transcript_support_level": null,
"aa_start": 1153,
"aa_end": null,
"aa_length": 1206,
"cds_start": 3457,
"cds_end": null,
"cds_length": 3621,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927921.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3454G>A",
"hgvs_p": "p.Ala1152Thr",
"transcript": "ENST00000927925.1",
"protein_id": "ENSP00000597984.1",
"transcript_support_level": null,
"aa_start": 1152,
"aa_end": null,
"aa_length": 1205,
"cds_start": 3454,
"cds_end": null,
"cds_length": 3618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927925.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3427G>A",
"hgvs_p": "p.Ala1143Thr",
"transcript": "ENST00000927922.1",
"protein_id": "ENSP00000597981.1",
"transcript_support_level": null,
"aa_start": 1143,
"aa_end": null,
"aa_length": 1196,
"cds_start": 3427,
"cds_end": null,
"cds_length": 3591,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927922.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3424G>A",
"hgvs_p": "p.Ala1142Thr",
"transcript": "ENST00000927923.1",
"protein_id": "ENSP00000597982.1",
"transcript_support_level": null,
"aa_start": 1142,
"aa_end": null,
"aa_length": 1195,
"cds_start": 3424,
"cds_end": null,
"cds_length": 3588,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927923.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3403G>A",
"hgvs_p": "p.Ala1135Thr",
"transcript": "ENST00000865171.1",
"protein_id": "ENSP00000535230.1",
"transcript_support_level": null,
"aa_start": 1135,
"aa_end": null,
"aa_length": 1188,
"cds_start": 3403,
"cds_end": null,
"cds_length": 3567,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865171.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "c.3400G>A",
"hgvs_p": "p.Ala1134Thr",
"transcript": "ENST00000927920.1",
"protein_id": "ENSP00000597979.1",
"transcript_support_level": null,
"aa_start": 1134,
"aa_end": null,
"aa_length": 1187,
"cds_start": 3400,
"cds_end": null,
"cds_length": 3564,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927920.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "n.2031G>A",
"hgvs_p": null,
"transcript": "ENST00000557589.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000557589.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"hgvs_c": "n.3600G>A",
"hgvs_p": null,
"transcript": "NR_138471.2",
"protein_id": null,
"transcript_support_level": null,
"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": "pseudogene",
"feature": "NR_138471.2"
}
],
"gene_symbol": "TIMELESS",
"gene_hgnc_id": 11813,
"dbsnp": "rs150055938",
"frequency_reference_population": 0.00012637823,
"hom_count_reference_population": 0,
"allele_count_reference_population": 204,
"gnomad_exomes_af": 0.0000690885,
"gnomad_genomes_af": 0.000676261,
"gnomad_exomes_ac": 101,
"gnomad_genomes_ac": 103,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.007472395896911621,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.007,
"revel_prediction": "Benign",
"alphamissense_score": 0.0635,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.78,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.591,
"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": -10,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Moderate,BS2",
"acmg_by_gene": [
{
"score": -10,
"benign_score": 10,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_003920.5",
"gene_symbol": "TIMELESS",
"hgnc_id": 11813,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.3463G>A",
"hgvs_p": "p.Ala1155Thr"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}