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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: 14-36517960-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=36517960&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 36517960,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000354822.7",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.524C>T",
"hgvs_p": "p.Ser175Leu",
"transcript": "NM_001079668.3",
"protein_id": "NP_001073136.1",
"transcript_support_level": null,
"aa_start": 175,
"aa_end": null,
"aa_length": 401,
"cds_start": 524,
"cds_end": null,
"cds_length": 1206,
"cdna_start": 627,
"cdna_end": null,
"cdna_length": 2190,
"mane_select": "ENST00000354822.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.524C>T",
"hgvs_p": "p.Ser175Leu",
"transcript": "ENST00000354822.7",
"protein_id": "ENSP00000346879.6",
"transcript_support_level": 1,
"aa_start": 175,
"aa_end": null,
"aa_length": 401,
"cds_start": 524,
"cds_end": null,
"cds_length": 1206,
"cdna_start": 627,
"cdna_end": null,
"cdna_length": 2190,
"mane_select": "NM_001079668.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.434C>T",
"hgvs_p": "p.Ser145Leu",
"transcript": "ENST00000498187.6",
"protein_id": "ENSP00000429607.2",
"transcript_support_level": 1,
"aa_start": 145,
"aa_end": null,
"aa_length": 371,
"cds_start": 434,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 770,
"cdna_end": null,
"cdna_length": 2338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.434C>T",
"hgvs_p": "p.Ser145Leu",
"transcript": "ENST00000522719.4",
"protein_id": "ENSP00000429519.4",
"transcript_support_level": 1,
"aa_start": 145,
"aa_end": null,
"aa_length": 371,
"cds_start": 434,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1219,
"cdna_end": null,
"cdna_length": 1962,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "SFTA3",
"gene_hgnc_id": null,
"hgvs_c": "n.373+1025C>T",
"hgvs_p": null,
"transcript": "ENST00000546983.2",
"protein_id": "ENSP00000449302.2",
"transcript_support_level": 4,
"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": 1664,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.434C>T",
"hgvs_p": "p.Ser145Leu",
"transcript": "NM_003317.4",
"protein_id": "NP_003308.1",
"transcript_support_level": null,
"aa_start": 145,
"aa_end": null,
"aa_length": 371,
"cds_start": 434,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 633,
"cdna_end": null,
"cdna_length": 2196,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"hgvs_c": "c.434C>T",
"hgvs_p": "p.Ser145Leu",
"transcript": "ENST00000518149.5",
"protein_id": "ENSP00000428341.1",
"transcript_support_level": 5,
"aa_start": 145,
"aa_end": null,
"aa_length": 371,
"cds_start": 434,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1040,
"cdna_end": null,
"cdna_length": 2583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SFTA3",
"gene_hgnc_id": null,
"hgvs_c": "n.54+1508C>T",
"hgvs_p": null,
"transcript": "ENST00000521945.1",
"protein_id": null,
"transcript_support_level": 2,
"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": 1116,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ENSG00000283098",
"gene_hgnc_id": null,
"hgvs_c": "n.322+69123G>A",
"hgvs_p": null,
"transcript": "ENST00000634305.1",
"protein_id": null,
"transcript_support_level": 5,
"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": 1737,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SFTA3",
"gene_hgnc_id": 18387,
"hgvs_c": "n.89+1508C>T",
"hgvs_p": null,
"transcript": "NR_161364.1",
"protein_id": null,
"transcript_support_level": null,
"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": 1106,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SFTA3",
"gene_hgnc_id": 18387,
"hgvs_c": "n.89+1508C>T",
"hgvs_p": null,
"transcript": "NR_161365.1",
"protein_id": null,
"transcript_support_level": null,
"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": 1070,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "NKX2-1",
"gene_hgnc_id": 11825,
"dbsnp": "rs863225300",
"frequency_reference_population": 6.9025117e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.90251e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3171989917755127,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.367,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.2089,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.08,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 4.077,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000354822.7",
"gene_symbol": "NKX2-1",
"hgnc_id": 11825,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.524C>T",
"hgvs_p": "p.Ser175Leu"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000546983.2",
"gene_symbol": "SFTA3",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.373+1025C>T",
"hgvs_p": null
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000634305.1",
"gene_symbol": "ENSG00000283098",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.322+69123G>A",
"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
}