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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: 22-40219272-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=40219272&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 40219272,
"ref": "G",
"alt": "T",
"effect": "intron_variant",
"transcript": "NM_001162501.2",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "NM_001162501.2",
"protein_id": "NP_001155973.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1833,
"cds_start": null,
"cds_end": null,
"cds_length": 5502,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000454349.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001162501.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000454349.7",
"protein_id": "ENSP00000401946.2",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 1833,
"cds_start": null,
"cds_end": null,
"cds_length": 5502,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001162501.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000454349.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000335727.13",
"protein_id": "ENSP00000338371.8",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1723,
"cds_start": null,
"cds_end": null,
"cds_length": 5172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000335727.13"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.114-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000402203.5",
"protein_id": "ENSP00000384795.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1029,
"cds_start": null,
"cds_end": null,
"cds_length": 3090,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402203.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000949217.1",
"protein_id": "ENSP00000619276.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1783,
"cds_start": null,
"cds_end": null,
"cds_length": 5352,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949217.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000921024.1",
"protein_id": "ENSP00000591083.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1780,
"cds_start": null,
"cds_end": null,
"cds_length": 5343,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921024.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000878235.1",
"protein_id": "ENSP00000548294.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1776,
"cds_start": null,
"cds_end": null,
"cds_length": 5331,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878235.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "NM_015088.3",
"protein_id": "NP_055903.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1723,
"cds_start": null,
"cds_end": null,
"cds_length": 5172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015088.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000921023.1",
"protein_id": "ENSP00000591082.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1664,
"cds_start": null,
"cds_end": null,
"cds_length": 4995,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921023.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.114-26743G>T",
"hgvs_p": null,
"transcript": "NM_001024843.2",
"protein_id": "NP_001020014.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1029,
"cds_start": null,
"cds_end": null,
"cds_length": 3090,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001024843.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.114-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000301923.13",
"protein_id": "ENSP00000306759.9",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1029,
"cds_start": null,
"cds_end": null,
"cds_length": 3090,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000301923.13"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000878236.1",
"protein_id": "ENSP00000548295.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 993,
"cds_start": null,
"cds_end": null,
"cds_length": 2982,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878236.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000878237.1",
"protein_id": "ENSP00000548296.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 940,
"cds_start": null,
"cds_end": null,
"cds_length": 2823,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878237.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000921025.1",
"protein_id": "ENSP00000591084.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 826,
"cds_start": null,
"cds_end": null,
"cds_length": 2481,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921025.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"hgvs_c": "n.217-26743G>T",
"hgvs_p": null,
"transcript": "ENST00000489500.1",
"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": "ENST00000489500.1"
}
],
"gene_symbol": "TNRC6B",
"gene_hgnc_id": 29190,
"dbsnp": "rs739182",
"frequency_reference_population": 0.29341364,
"hom_count_reference_population": 7592,
"allele_count_reference_population": 44620,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.293414,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 44620,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 7592,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.9100000262260437,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.91,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.313,
"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": "NM_001162501.2",
"gene_symbol": "TNRC6B",
"hgnc_id": 29190,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.6-26743G>T",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}