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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: 9-83000462-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=83000462&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 83000462,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_152573.4",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1546A>G",
"hgvs_p": "p.Arg516Gly",
"transcript": "NM_152573.4",
"protein_id": "NP_689786.2",
"transcript_support_level": null,
"aa_start": 516,
"aa_end": null,
"aa_length": 740,
"cds_start": 1546,
"cds_end": null,
"cds_length": 2223,
"cdna_start": 1821,
"cdna_end": null,
"cdna_length": 5585,
"mane_select": "ENST00000376447.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_152573.4"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1546A>G",
"hgvs_p": "p.Arg516Gly",
"transcript": "ENST00000376447.4",
"protein_id": "ENSP00000365630.3",
"transcript_support_level": 1,
"aa_start": 516,
"aa_end": null,
"aa_length": 740,
"cds_start": 1546,
"cds_end": null,
"cds_length": 2223,
"cdna_start": 1821,
"cdna_end": null,
"cdna_length": 5585,
"mane_select": "NM_152573.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376447.4"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1546A>G",
"hgvs_p": "p.Arg516Gly",
"transcript": "ENST00000928035.1",
"protein_id": "ENSP00000598094.1",
"transcript_support_level": null,
"aa_start": 516,
"aa_end": null,
"aa_length": 735,
"cds_start": 1546,
"cds_end": null,
"cds_length": 2208,
"cdna_start": 1934,
"cdna_end": null,
"cdna_length": 5681,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928035.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1477A>G",
"hgvs_p": "p.Arg493Gly",
"transcript": "ENST00000873431.1",
"protein_id": "ENSP00000543490.1",
"transcript_support_level": null,
"aa_start": 493,
"aa_end": null,
"aa_length": 717,
"cds_start": 1477,
"cds_end": null,
"cds_length": 2154,
"cdna_start": 1799,
"cdna_end": null,
"cdna_length": 5563,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000873431.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1468A>G",
"hgvs_p": "p.Arg490Gly",
"transcript": "ENST00000873434.1",
"protein_id": "ENSP00000543493.1",
"transcript_support_level": null,
"aa_start": 490,
"aa_end": null,
"aa_length": 714,
"cds_start": 1468,
"cds_end": null,
"cds_length": 2145,
"cdna_start": 1489,
"cdna_end": null,
"cdna_length": 2457,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000873434.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1399A>G",
"hgvs_p": "p.Arg467Gly",
"transcript": "ENST00000873432.1",
"protein_id": "ENSP00000543491.1",
"transcript_support_level": null,
"aa_start": 467,
"aa_end": null,
"aa_length": 691,
"cds_start": 1399,
"cds_end": null,
"cds_length": 2076,
"cdna_start": 1684,
"cdna_end": null,
"cdna_length": 5448,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000873432.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1330A>G",
"hgvs_p": "p.Arg444Gly",
"transcript": "ENST00000873433.1",
"protein_id": "ENSP00000543492.1",
"transcript_support_level": null,
"aa_start": 444,
"aa_end": null,
"aa_length": 668,
"cds_start": 1330,
"cds_end": null,
"cds_length": 2007,
"cdna_start": 1605,
"cdna_end": null,
"cdna_length": 5369,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000873433.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1477A>G",
"hgvs_p": "p.Arg493Gly",
"transcript": "XM_005251730.5",
"protein_id": "XP_005251787.1",
"transcript_support_level": null,
"aa_start": 493,
"aa_end": null,
"aa_length": 717,
"cds_start": 1477,
"cds_end": null,
"cds_length": 2154,
"cdna_start": 1752,
"cdna_end": null,
"cdna_length": 5516,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005251730.5"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1159A>G",
"hgvs_p": "p.Arg387Gly",
"transcript": "XM_005251731.5",
"protein_id": "XP_005251788.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 611,
"cds_start": 1159,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 2293,
"cdna_end": null,
"cdna_length": 6057,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005251731.5"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.1090A>G",
"hgvs_p": "p.Arg364Gly",
"transcript": "XM_047422826.1",
"protein_id": "XP_047278782.1",
"transcript_support_level": null,
"aa_start": 364,
"aa_end": null,
"aa_length": 588,
"cds_start": 1090,
"cds_end": null,
"cds_length": 1767,
"cdna_start": 2224,
"cdna_end": null,
"cdna_length": 5988,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047422826.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"hgvs_c": "c.997A>G",
"hgvs_p": "p.Arg333Gly",
"transcript": "XM_047422827.1",
"protein_id": "XP_047278783.1",
"transcript_support_level": null,
"aa_start": 333,
"aa_end": null,
"aa_length": 557,
"cds_start": 997,
"cds_end": null,
"cds_length": 1674,
"cdna_start": 1304,
"cdna_end": null,
"cdna_length": 5068,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047422827.1"
}
],
"gene_symbol": "RASEF",
"gene_hgnc_id": 26464,
"dbsnp": "rs147216417",
"frequency_reference_population": 0.0007645137,
"hom_count_reference_population": 1,
"allele_count_reference_population": 1234,
"gnomad_exomes_af": 0.000774367,
"gnomad_genomes_af": 0.000669916,
"gnomad_exomes_ac": 1132,
"gnomad_genomes_ac": 102,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0632442831993103,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.267,
"revel_prediction": "Benign",
"alphamissense_score": 0.2473,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.09,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.146,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_152573.4",
"gene_symbol": "RASEF",
"hgnc_id": 26464,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1546A>G",
"hgvs_p": "p.Arg516Gly"
}
],
"clinvar_disease": "RASEF-related disorder",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "RASEF-related disorder",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}