← 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: 7-94663767-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=94663767&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 94663767,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001172437.2",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.439C>G",
"hgvs_p": "p.Pro147Ala",
"transcript": "ENST00000612748.1",
"protein_id": "ENSP00000480676.1",
"transcript_support_level": 5,
"aa_start": 147,
"aa_end": null,
"aa_length": 783,
"cds_start": 439,
"cds_end": null,
"cds_length": 2352,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000612748.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.313C>G",
"hgvs_p": "p.Pro105Ala",
"transcript": "ENST00000615790.5",
"protein_id": "ENSP00000482653.2",
"transcript_support_level": 1,
"aa_start": 105,
"aa_end": null,
"aa_length": 359,
"cds_start": 313,
"cds_end": null,
"cds_length": 1080,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000615790.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000482108.1",
"protein_id": "ENSP00000417587.1",
"transcript_support_level": 1,
"aa_start": 71,
"aa_end": null,
"aa_length": 325,
"cds_start": 211,
"cds_end": null,
"cds_length": 978,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000482108.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.439C>G",
"hgvs_p": "p.Pro147Ala",
"transcript": "NM_001172437.2",
"protein_id": "NP_001165908.1",
"transcript_support_level": null,
"aa_start": 147,
"aa_end": null,
"aa_length": 783,
"cds_start": 439,
"cds_end": null,
"cds_length": 2354,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001172437.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.313C>G",
"hgvs_p": "p.Pro105Ala",
"transcript": "NM_001184961.1",
"protein_id": "NP_001171890.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 741,
"cds_start": 313,
"cds_end": null,
"cds_length": 2228,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001184961.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.313C>G",
"hgvs_p": "p.Pro105Ala",
"transcript": "ENST00000612941.2",
"protein_id": "ENSP00000478744.2",
"transcript_support_level": 5,
"aa_start": 105,
"aa_end": null,
"aa_length": 741,
"cds_start": 313,
"cds_end": null,
"cds_length": 2226,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000612941.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "NM_015068.3",
"protein_id": "NP_055883.2",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 707,
"cds_start": 211,
"cds_end": null,
"cds_length": 2126,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015068.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000617526.4",
"protein_id": "ENSP00000481101.1",
"transcript_support_level": 5,
"aa_start": 71,
"aa_end": null,
"aa_length": 707,
"cds_start": 211,
"cds_end": null,
"cds_length": 2124,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000617526.4"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.439C>G",
"hgvs_p": "p.Pro147Ala",
"transcript": "NM_001172438.3",
"protein_id": "NP_001165909.1",
"transcript_support_level": null,
"aa_start": 147,
"aa_end": null,
"aa_length": 401,
"cds_start": 439,
"cds_end": null,
"cds_length": 1206,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001172438.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.439C>G",
"hgvs_p": "p.Pro147Ala",
"transcript": "ENST00000488574.5",
"protein_id": "ENSP00000418944.2",
"transcript_support_level": 2,
"aa_start": 147,
"aa_end": null,
"aa_length": 401,
"cds_start": 439,
"cds_end": null,
"cds_length": 1206,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000488574.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.313C>G",
"hgvs_p": "p.Pro105Ala",
"transcript": "NM_001184962.2",
"protein_id": "NP_001171891.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 359,
"cds_start": 313,
"cds_end": null,
"cds_length": 1080,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001184962.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "NM_001040152.2",
"protein_id": "NP_001035242.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 325,
"cds_start": 211,
"cds_end": null,
"cds_length": 978,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001040152.2"
},
{
"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": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "n.307+338C>G",
"hgvs_p": null,
"transcript": "ENST00000493935.1",
"protein_id": null,
"transcript_support_level": 4,
"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": "ENST00000493935.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"hgvs_c": "c.*117C>G",
"hgvs_p": null,
"transcript": "ENST00000613043.1",
"protein_id": "ENSP00000482046.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 30,
"cds_start": null,
"cds_end": null,
"cds_length": 94,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000613043.1"
}
],
"gene_symbol": "PEG10",
"gene_hgnc_id": 14005,
"dbsnp": "rs776875257",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.0000065697,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.039380550384521484,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.021,
"revel_prediction": "Benign",
"alphamissense_score": 0.0521,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.6,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.583,
"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_001172437.2",
"gene_symbol": "PEG10",
"hgnc_id": 14005,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.439C>G",
"hgvs_p": "p.Pro147Ala"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}