← 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: 1-109236451-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=109236451&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 109236451,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001330669.1",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "NM_006513.4",
"protein_id": "NP_006504.2",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 514,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000234677.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006513.4"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000234677.7",
"protein_id": "ENSP00000234677.2",
"transcript_support_level": 1,
"aa_start": 387,
"aa_end": null,
"aa_length": 514,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_006513.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000234677.7"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1277G>A",
"hgvs_p": "p.Gly426Glu",
"transcript": "ENST00000943750.1",
"protein_id": "ENSP00000613809.1",
"transcript_support_level": null,
"aa_start": 426,
"aa_end": null,
"aa_length": 575,
"cds_start": 1277,
"cds_end": null,
"cds_length": 1728,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943750.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1277G>A",
"hgvs_p": "p.Gly426Glu",
"transcript": "ENST00000943751.1",
"protein_id": "ENSP00000613810.1",
"transcript_support_level": null,
"aa_start": 426,
"aa_end": null,
"aa_length": 553,
"cds_start": 1277,
"cds_end": null,
"cds_length": 1662,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943751.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000943753.1",
"protein_id": "ENSP00000613812.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 545,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1638,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943753.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000854548.1",
"protein_id": "ENSP00000524607.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 539,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1620,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854548.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1232G>A",
"hgvs_p": "p.Gly411Glu",
"transcript": "ENST00000943752.1",
"protein_id": "ENSP00000613811.1",
"transcript_support_level": null,
"aa_start": 411,
"aa_end": null,
"aa_length": 538,
"cds_start": 1232,
"cds_end": null,
"cds_length": 1617,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943752.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "NM_001330669.1",
"protein_id": "NP_001317598.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 536,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1611,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001330669.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000369923.4",
"protein_id": "ENSP00000358939.4",
"transcript_support_level": 5,
"aa_start": 387,
"aa_end": null,
"aa_length": 536,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1611,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000369923.4"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000854549.1",
"protein_id": "ENSP00000524608.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 526,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1581,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854549.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000854545.1",
"protein_id": "ENSP00000524604.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 523,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854545.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1181G>A",
"hgvs_p": "p.Gly394Glu",
"transcript": "ENST00000854546.1",
"protein_id": "ENSP00000524605.1",
"transcript_support_level": null,
"aa_start": 394,
"aa_end": null,
"aa_length": 521,
"cds_start": 1181,
"cds_end": null,
"cds_length": 1566,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854546.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000933282.1",
"protein_id": "ENSP00000603341.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 514,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933282.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu",
"transcript": "ENST00000933281.1",
"protein_id": "ENSP00000603340.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 512,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1539,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933281.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1151G>A",
"hgvs_p": "p.Gly384Glu",
"transcript": "ENST00000943754.1",
"protein_id": "ENSP00000613813.1",
"transcript_support_level": null,
"aa_start": 384,
"aa_end": null,
"aa_length": 511,
"cds_start": 1151,
"cds_end": null,
"cds_length": 1536,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943754.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1097G>A",
"hgvs_p": "p.Gly366Glu",
"transcript": "ENST00000943756.1",
"protein_id": "ENSP00000613815.1",
"transcript_support_level": null,
"aa_start": 366,
"aa_end": null,
"aa_length": 493,
"cds_start": 1097,
"cds_end": null,
"cds_length": 1482,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943756.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1073G>A",
"hgvs_p": "p.Gly358Glu",
"transcript": "ENST00000933284.1",
"protein_id": "ENSP00000603343.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 485,
"cds_start": 1073,
"cds_end": null,
"cds_length": 1458,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933284.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Glu",
"transcript": "ENST00000854547.1",
"protein_id": "ENSP00000524606.1",
"transcript_support_level": null,
"aa_start": 353,
"aa_end": null,
"aa_length": 480,
"cds_start": 1058,
"cds_end": null,
"cds_length": 1443,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854547.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1016G>A",
"hgvs_p": "p.Gly339Glu",
"transcript": "ENST00000854550.1",
"protein_id": "ENSP00000524609.1",
"transcript_support_level": null,
"aa_start": 339,
"aa_end": null,
"aa_length": 466,
"cds_start": 1016,
"cds_end": null,
"cds_length": 1401,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000854550.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.1004G>A",
"hgvs_p": "p.Gly335Glu",
"transcript": "ENST00000943755.1",
"protein_id": "ENSP00000613814.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 462,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1389,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943755.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000933283.1",
"protein_id": "ENSP00000603342.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 459,
"cds_start": 995,
"cds_end": null,
"cds_length": 1380,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933283.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"hgvs_c": "n.221G>A",
"hgvs_p": null,
"transcript": "ENST00000468588.1",
"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": "pseudogene",
"feature": "ENST00000468588.1"
}
],
"gene_symbol": "SARS1",
"gene_hgnc_id": 10537,
"dbsnp": "rs140717526",
"frequency_reference_population": 0.011671231,
"hom_count_reference_population": 158,
"allele_count_reference_population": 18726,
"gnomad_exomes_af": 0.0119594,
"gnomad_genomes_af": 0.00892165,
"gnomad_exomes_ac": 17368,
"gnomad_genomes_ac": 1358,
"gnomad_exomes_homalt": 143,
"gnomad_genomes_homalt": 15,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.009588867425918579,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.316,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.2404,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.28,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.583,
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001330669.1",
"gene_symbol": "SARS1",
"hgnc_id": 10537,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.1160G>A",
"hgvs_p": "p.Gly387Glu"
}
],
"clinvar_disease": " alkalosis syndrome, pulmonary hypertension, renal failure,Hyperuricemia,not provided",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:1 B:3",
"phenotype_combined": "not provided|Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}