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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: 15-40016658-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=40016658&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 40016658,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001013703.4",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser",
"transcript": "NM_001013703.4",
"protein_id": "NP_001013725.2",
"transcript_support_level": null,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1649,
"cds_start": 3916,
"cds_end": null,
"cds_length": 4950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000263791.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001013703.4"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser",
"transcript": "ENST00000263791.10",
"protein_id": "ENSP00000263791.5",
"transcript_support_level": 2,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1649,
"cds_start": 3916,
"cds_end": null,
"cds_length": 4950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001013703.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000263791.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "n.2833G>A",
"hgvs_p": null,
"transcript": "ENST00000558629.5",
"protein_id": null,
"transcript_support_level": 1,
"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": "retained_intron",
"feature": "ENST00000558629.5"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3958G>A",
"hgvs_p": "p.Gly1320Ser",
"transcript": "ENST00000917949.1",
"protein_id": "ENSP00000588008.1",
"transcript_support_level": null,
"aa_start": 1320,
"aa_end": null,
"aa_length": 1663,
"cds_start": 3958,
"cds_end": null,
"cds_length": 4992,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917949.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser",
"transcript": "ENST00000917947.1",
"protein_id": "ENSP00000588006.1",
"transcript_support_level": null,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1626,
"cds_start": 3916,
"cds_end": null,
"cds_length": 4881,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917947.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3835G>A",
"hgvs_p": "p.Gly1279Ser",
"transcript": "ENST00000917953.1",
"protein_id": "ENSP00000588012.1",
"transcript_support_level": null,
"aa_start": 1279,
"aa_end": null,
"aa_length": 1622,
"cds_start": 3835,
"cds_end": null,
"cds_length": 4869,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917953.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser",
"transcript": "ENST00000917948.1",
"protein_id": "ENSP00000588007.1",
"transcript_support_level": null,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1613,
"cds_start": 3916,
"cds_end": null,
"cds_length": 4842,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917948.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3832G>A",
"hgvs_p": "p.Gly1278Ser",
"transcript": "ENST00000917950.1",
"protein_id": "ENSP00000588009.1",
"transcript_support_level": null,
"aa_start": 1278,
"aa_end": null,
"aa_length": 1598,
"cds_start": 3832,
"cds_end": null,
"cds_length": 4797,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917950.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser",
"transcript": "ENST00000917945.1",
"protein_id": "ENSP00000588004.1",
"transcript_support_level": null,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1577,
"cds_start": 3916,
"cds_end": null,
"cds_length": 4734,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917945.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3247G>A",
"hgvs_p": "p.Gly1083Ser",
"transcript": "ENST00000560855.5",
"protein_id": "ENSP00000453575.1",
"transcript_support_level": 5,
"aa_start": 1083,
"aa_end": null,
"aa_length": 1426,
"cds_start": 3247,
"cds_end": null,
"cds_length": 4281,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000560855.5"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3220G>A",
"hgvs_p": "p.Gly1074Ser",
"transcript": "ENST00000917951.1",
"protein_id": "ENSP00000588010.1",
"transcript_support_level": null,
"aa_start": 1074,
"aa_end": null,
"aa_length": 1417,
"cds_start": 3220,
"cds_end": null,
"cds_length": 4254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917951.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": 27,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3760-450G>A",
"hgvs_p": null,
"transcript": "ENST00000917946.1",
"protein_id": "ENSP00000588005.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1592,
"cds_start": null,
"cds_end": null,
"cds_length": 4779,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917946.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": 27,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3760-450G>A",
"hgvs_p": null,
"transcript": "ENST00000958415.1",
"protein_id": "ENSP00000628474.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1569,
"cds_start": null,
"cds_end": null,
"cds_length": 4710,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958415.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3676-450G>A",
"hgvs_p": null,
"transcript": "ENST00000917952.1",
"protein_id": "ENSP00000588011.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1564,
"cds_start": null,
"cds_end": null,
"cds_length": 4695,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917952.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": 27,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "c.3760-450G>A",
"hgvs_p": null,
"transcript": "ENST00000958416.1",
"protein_id": "ENSP00000628475.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1556,
"cds_start": null,
"cds_end": null,
"cds_length": 4671,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958416.1"
},
{
"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": 17,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"hgvs_c": "n.923-450G>A",
"hgvs_p": null,
"transcript": "ENST00000558557.1",
"protein_id": null,
"transcript_support_level": 2,
"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": "retained_intron",
"feature": "ENST00000558557.1"
},
{
"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": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000306490",
"gene_hgnc_id": null,
"hgvs_c": "n.195+5993C>T",
"hgvs_p": null,
"transcript": "ENST00000819059.1",
"protein_id": null,
"transcript_support_level": null,
"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": "ENST00000819059.1"
}
],
"gene_symbol": "EIF2AK4",
"gene_hgnc_id": 19687,
"dbsnp": "rs35602605",
"frequency_reference_population": 0.00005391009,
"hom_count_reference_population": 0,
"allele_count_reference_population": 87,
"gnomad_exomes_af": 0.0000513103,
"gnomad_genomes_af": 0.0000788934,
"gnomad_exomes_ac": 75,
"gnomad_genomes_ac": 12,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8244689106941223,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.07000000029802322,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.254,
"revel_prediction": "Benign",
"alphamissense_score": 0.1357,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.06,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 7.903,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.07,
"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": "PP3",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 0,
"pathogenic_score": 1,
"criteria": [
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001013703.4",
"gene_symbol": "EIF2AK4",
"hgnc_id": 19687,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.3916G>A",
"hgvs_p": "p.Gly1306Ser"
},
{
"score": 1,
"benign_score": 0,
"pathogenic_score": 1,
"criteria": [
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000819059.1",
"gene_symbol": "ENSG00000306490",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.195+5993C>T",
"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
}