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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: 12-57466263-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=57466263&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 57466263,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "ENST00000228682.7",
"consequences": [
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.786C>T",
"hgvs_p": "p.His262His",
"transcript": "NM_005269.3",
"protein_id": "NP_005260.1",
"transcript_support_level": null,
"aa_start": 262,
"aa_end": null,
"aa_length": 1106,
"cds_start": 786,
"cds_end": null,
"cds_length": 3321,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 3972,
"mane_select": "ENST00000228682.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.786C>T",
"hgvs_p": "p.His262His",
"transcript": "ENST00000228682.7",
"protein_id": "ENSP00000228682.2",
"transcript_support_level": 1,
"aa_start": 262,
"aa_end": null,
"aa_length": 1106,
"cds_start": 786,
"cds_end": null,
"cds_length": 3321,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 3972,
"mane_select": "NM_005269.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.663C>T",
"hgvs_p": "p.His221His",
"transcript": "ENST00000528467.1",
"protein_id": "ENSP00000434408.1",
"transcript_support_level": 1,
"aa_start": 221,
"aa_end": null,
"aa_length": 1064,
"cds_start": 663,
"cds_end": null,
"cds_length": 3196,
"cdna_start": 663,
"cdna_end": null,
"cdna_length": 3196,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.663C>T",
"hgvs_p": "p.His221His",
"transcript": "NM_001167609.2",
"protein_id": "NP_001161081.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 1065,
"cds_start": 663,
"cds_end": null,
"cds_length": 3198,
"cdna_start": 1107,
"cdna_end": null,
"cdna_length": 3849,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.663C>T",
"hgvs_p": "p.His221His",
"transcript": "ENST00000546141.5",
"protein_id": "ENSP00000441006.1",
"transcript_support_level": 5,
"aa_start": 221,
"aa_end": null,
"aa_length": 1065,
"cds_start": 663,
"cds_end": null,
"cds_length": 3198,
"cdna_start": 741,
"cdna_end": null,
"cdna_length": 3475,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.402C>T",
"hgvs_p": "p.His134His",
"transcript": "NM_001160045.2",
"protein_id": "NP_001153517.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 978,
"cds_start": 402,
"cds_end": null,
"cds_length": 2937,
"cdna_start": 1010,
"cdna_end": null,
"cdna_length": 3752,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.402C>T",
"hgvs_p": "p.His134His",
"transcript": "ENST00000543426.5",
"protein_id": "ENSP00000437607.1",
"transcript_support_level": 5,
"aa_start": 134,
"aa_end": null,
"aa_length": 978,
"cds_start": 402,
"cds_end": null,
"cds_length": 2937,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 3394,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.402C>T",
"hgvs_p": "p.His134His",
"transcript": "ENST00000532291.5",
"protein_id": "ENSP00000436671.1",
"transcript_support_level": 4,
"aa_start": 134,
"aa_end": null,
"aa_length": 174,
"cds_start": 402,
"cds_end": null,
"cds_length": 526,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 784,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.786C>T",
"hgvs_p": "p.His262His",
"transcript": "XM_011538189.3",
"protein_id": "XP_011536491.1",
"transcript_support_level": null,
"aa_start": 262,
"aa_end": null,
"aa_length": 1106,
"cds_start": 786,
"cds_end": null,
"cds_length": 3321,
"cdna_start": 1092,
"cdna_end": null,
"cdna_length": 3834,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "H",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "c.786C>T",
"hgvs_p": "p.His262His",
"transcript": "XM_011538190.3",
"protein_id": "XP_011536492.1",
"transcript_support_level": null,
"aa_start": 262,
"aa_end": null,
"aa_length": 1029,
"cds_start": 786,
"cds_end": null,
"cds_length": 3090,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 3741,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"hgvs_c": "n.*122C>T",
"hgvs_p": null,
"transcript": "ENST00000527742.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 676,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "GLI1",
"gene_hgnc_id": 4317,
"dbsnp": "rs7973381",
"frequency_reference_population": 0.025916591,
"hom_count_reference_population": 1308,
"allele_count_reference_population": 41813,
"gnomad_exomes_af": 0.0227423,
"gnomad_genomes_af": 0.0563975,
"gnomad_exomes_ac": 33231,
"gnomad_genomes_ac": 8582,
"gnomad_exomes_homalt": 817,
"gnomad_genomes_homalt": 491,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.6499999761581421,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.65,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.838,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": -14,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BP7,BA1",
"acmg_by_gene": [
{
"score": -14,
"benign_score": 14,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000228682.7",
"gene_symbol": "GLI1",
"hgnc_id": 4317,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR,AD,Unknown",
"hgvs_c": "c.786C>T",
"hgvs_p": "p.His262His"
}
],
"clinvar_disease": "GLI1-related disorder",
"clinvar_classification": "Benign",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "GLI1-related disorder",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}