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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: 14-56296793-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=56296793&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 56296793,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_021255.3",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.890A>G",
"hgvs_p": "p.Asn297Ser",
"transcript": "NM_021255.3",
"protein_id": "NP_067078.1",
"transcript_support_level": null,
"aa_start": 297,
"aa_end": null,
"aa_length": 420,
"cds_start": 890,
"cds_end": null,
"cds_length": 1263,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000267460.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_021255.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.890A>G",
"hgvs_p": "p.Asn297Ser",
"transcript": "ENST00000267460.9",
"protein_id": "ENSP00000267460.4",
"transcript_support_level": 1,
"aa_start": 297,
"aa_end": null,
"aa_length": 420,
"cds_start": 890,
"cds_end": null,
"cds_length": 1263,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_021255.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000267460.9"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.1061A>G",
"hgvs_p": "p.Asn354Ser",
"transcript": "ENST00000705193.1",
"protein_id": "ENSP00000516089.1",
"transcript_support_level": null,
"aa_start": 354,
"aa_end": null,
"aa_length": 477,
"cds_start": 1061,
"cds_end": null,
"cds_length": 1434,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000705193.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.851A>G",
"hgvs_p": "p.Asn284Ser",
"transcript": "XM_017021478.2",
"protein_id": "XP_016876967.1",
"transcript_support_level": null,
"aa_start": 284,
"aa_end": null,
"aa_length": 407,
"cds_start": 851,
"cds_end": null,
"cds_length": 1224,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017021478.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.590A>G",
"hgvs_p": "p.Asn197Ser",
"transcript": "XM_006720211.4",
"protein_id": "XP_006720274.1",
"transcript_support_level": null,
"aa_start": 197,
"aa_end": null,
"aa_length": 320,
"cds_start": 590,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006720211.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.590A>G",
"hgvs_p": "p.Asn197Ser",
"transcript": "XM_011536990.3",
"protein_id": "XP_011535292.1",
"transcript_support_level": null,
"aa_start": 197,
"aa_end": null,
"aa_length": 320,
"cds_start": 590,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536990.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.590A>G",
"hgvs_p": "p.Asn197Ser",
"transcript": "XM_011536992.4",
"protein_id": "XP_011535294.1",
"transcript_support_level": null,
"aa_start": 197,
"aa_end": null,
"aa_length": 320,
"cds_start": 590,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536992.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.590A>G",
"hgvs_p": "p.Asn197Ser",
"transcript": "XM_017021479.2",
"protein_id": "XP_016876968.1",
"transcript_support_level": null,
"aa_start": 197,
"aa_end": null,
"aa_length": 320,
"cds_start": 590,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017021479.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"hgvs_c": "c.590A>G",
"hgvs_p": "p.Asn197Ser",
"transcript": "XM_047431612.1",
"protein_id": "XP_047287568.1",
"transcript_support_level": null,
"aa_start": 197,
"aa_end": null,
"aa_length": 320,
"cds_start": 590,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431612.1"
}
],
"gene_symbol": "PELI2",
"gene_hgnc_id": 8828,
"dbsnp": "rs766481243",
"frequency_reference_population": 0.000035316334,
"hom_count_reference_population": 0,
"allele_count_reference_population": 57,
"gnomad_exomes_af": 0.0000342039,
"gnomad_genomes_af": 0.0000460036,
"gnomad_exomes_ac": 50,
"gnomad_genomes_ac": 7,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.019906550645828247,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.061,
"revel_prediction": "Benign",
"alphamissense_score": 0.0515,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.76,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.621,
"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": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_021255.3",
"gene_symbol": "PELI2",
"hgnc_id": 8828,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.890A>G",
"hgvs_p": "p.Asn297Ser"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}