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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: 3-49722239-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=49722239&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 49722239,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000308388.7",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu",
"transcript": "NM_021971.4",
"protein_id": "NP_068806.2",
"transcript_support_level": null,
"aa_start": 254,
"aa_end": null,
"aa_length": 360,
"cds_start": 760,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 985,
"cdna_end": null,
"cdna_length": 3144,
"mane_select": "ENST00000308388.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu",
"transcript": "ENST00000308388.7",
"protein_id": "ENSP00000311130.6",
"transcript_support_level": 1,
"aa_start": 254,
"aa_end": null,
"aa_length": 360,
"cds_start": 760,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 985,
"cdna_end": null,
"cdna_length": 3144,
"mane_select": "NM_021971.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.868G>C",
"hgvs_p": "p.Val290Leu",
"transcript": "ENST00000495627.2",
"protein_id": "ENSP00000503768.1",
"transcript_support_level": 2,
"aa_start": 290,
"aa_end": null,
"aa_length": 396,
"cds_start": 868,
"cds_end": null,
"cds_length": 1191,
"cdna_start": 1115,
"cdna_end": null,
"cdna_length": 1660,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu",
"transcript": "NM_013334.4",
"protein_id": "NP_037466.3",
"transcript_support_level": null,
"aa_start": 254,
"aa_end": null,
"aa_length": 387,
"cds_start": 760,
"cds_end": null,
"cds_length": 1164,
"cdna_start": 985,
"cdna_end": null,
"cdna_length": 1642,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu",
"transcript": "ENST00000308375.10",
"protein_id": "ENSP00000309092.6",
"transcript_support_level": 2,
"aa_start": 254,
"aa_end": null,
"aa_length": 387,
"cds_start": 760,
"cds_end": null,
"cds_length": 1164,
"cdna_start": 985,
"cdna_end": null,
"cdna_length": 3217,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu",
"transcript": "ENST00000480687.5",
"protein_id": "ENSP00000418565.1",
"transcript_support_level": 2,
"aa_start": 254,
"aa_end": null,
"aa_length": 360,
"cds_start": 760,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 877,
"cdna_end": null,
"cdna_length": 6108,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "n.1333G>C",
"hgvs_p": null,
"transcript": "ENST00000481959.2",
"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": 1795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "n.1194G>C",
"hgvs_p": null,
"transcript": "ENST00000678208.1",
"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": 2919,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "n.*51G>C",
"hgvs_p": null,
"transcript": "ENST00000678853.1",
"protein_id": "ENSP00000504692.1",
"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": 2389,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "n.*51G>C",
"hgvs_p": null,
"transcript": "ENST00000678853.1",
"protein_id": "ENSP00000504692.1",
"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": 2389,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.562-92G>C",
"hgvs_p": null,
"transcript": "ENST00000677393.1",
"protein_id": "ENSP00000503880.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 255,
"cds_start": -4,
"cds_end": null,
"cds_length": 768,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2510,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"hgvs_c": "c.403-92G>C",
"hgvs_p": null,
"transcript": "ENST00000678010.1",
"protein_id": "ENSP00000503176.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 238,
"cds_start": -4,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2048,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "GMPPB",
"gene_hgnc_id": 22932,
"dbsnp": "rs875989850",
"frequency_reference_population": 0.0000065698705,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.00000656987,
"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": 0.7940274477005005,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.731,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9004,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.31,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.675,
"phylop100way_prediction": "Pathogenic",
"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": 5,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PM5,PP3",
"acmg_by_gene": [
{
"score": 5,
"benign_score": 0,
"pathogenic_score": 5,
"criteria": [
"PM2",
"PM5",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000308388.7",
"gene_symbol": "GMPPB",
"hgnc_id": 22932,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.760G>C",
"hgvs_p": "p.Val254Leu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}