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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: 2-39056862-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=39056862&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 39056862,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000402219.8",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "NM_005633.4",
"protein_id": "NP_005624.2",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1333,
"cds_start": 350,
"cds_end": null,
"cds_length": 4002,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 8906,
"mane_select": "ENST00000402219.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "ENST00000402219.8",
"protein_id": "ENSP00000384675.2",
"transcript_support_level": 1,
"aa_start": 117,
"aa_end": null,
"aa_length": 1333,
"cds_start": 350,
"cds_end": null,
"cds_length": 4002,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 8906,
"mane_select": "NM_005633.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.329T>G",
"hgvs_p": "p.Val110Gly",
"transcript": "NM_001382394.1",
"protein_id": "NP_001369323.1",
"transcript_support_level": null,
"aa_start": 110,
"aa_end": null,
"aa_length": 1326,
"cds_start": 329,
"cds_end": null,
"cds_length": 3981,
"cdna_start": 468,
"cdna_end": null,
"cdna_length": 8395,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "NM_001382395.1",
"protein_id": "NP_001369324.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1318,
"cds_start": 350,
"cds_end": null,
"cds_length": 3957,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 8861,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "ENST00000395038.6",
"protein_id": "ENSP00000378479.2",
"transcript_support_level": 5,
"aa_start": 117,
"aa_end": null,
"aa_length": 1318,
"cds_start": 350,
"cds_end": null,
"cds_length": 3957,
"cdna_start": 378,
"cdna_end": null,
"cdna_length": 4123,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "ENST00000692089.1",
"protein_id": "ENSP00000508626.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1147,
"cds_start": 350,
"cds_end": null,
"cds_length": 3444,
"cdna_start": 367,
"cdna_end": null,
"cdna_length": 4056,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "ENST00000691229.1",
"protein_id": "ENSP00000510437.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1086,
"cds_start": 350,
"cds_end": null,
"cds_length": 3261,
"cdna_start": 367,
"cdna_end": null,
"cdna_length": 5976,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.179T>G",
"hgvs_p": "p.Val60Gly",
"transcript": "ENST00000451331.1",
"protein_id": "ENSP00000393899.1",
"transcript_support_level": 4,
"aa_start": 60,
"aa_end": null,
"aa_length": 101,
"cds_start": 179,
"cds_end": null,
"cds_length": 308,
"cdna_start": 450,
"cdna_end": null,
"cdna_length": 579,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.329T>G",
"hgvs_p": "p.Val110Gly",
"transcript": "XM_047445581.1",
"protein_id": "XP_047301537.1",
"transcript_support_level": null,
"aa_start": 110,
"aa_end": null,
"aa_length": 1311,
"cds_start": 329,
"cds_end": null,
"cds_length": 3936,
"cdna_start": 468,
"cdna_end": null,
"cdna_length": 8350,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.179T>G",
"hgvs_p": "p.Val60Gly",
"transcript": "XM_011533064.3",
"protein_id": "XP_011531366.1",
"transcript_support_level": null,
"aa_start": 60,
"aa_end": null,
"aa_length": 1276,
"cds_start": 179,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 3939,
"cdna_end": null,
"cdna_length": 11866,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.179T>G",
"hgvs_p": "p.Val60Gly",
"transcript": "XM_047445582.1",
"protein_id": "XP_047301538.1",
"transcript_support_level": null,
"aa_start": 60,
"aa_end": null,
"aa_length": 1276,
"cds_start": 179,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 569,
"cdna_end": null,
"cdna_length": 8496,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "XM_047445583.1",
"protein_id": "XP_047301539.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1187,
"cds_start": 350,
"cds_end": null,
"cds_length": 3564,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 7951,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly",
"transcript": "XM_047445584.1",
"protein_id": "XP_047301540.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 1172,
"cds_start": 350,
"cds_end": null,
"cds_length": 3519,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 7906,
"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": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.377T>G",
"hgvs_p": null,
"transcript": "ENST00000461545.2",
"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": 1608,
"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": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.1188T>G",
"hgvs_p": null,
"transcript": "ENST00000685782.1",
"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": 2352,
"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": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.115T>G",
"hgvs_p": null,
"transcript": "ENST00000688189.1",
"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": 1451,
"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": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.357T>G",
"hgvs_p": null,
"transcript": "ENST00000689668.1",
"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": 3407,
"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": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.449T>G",
"hgvs_p": null,
"transcript": "ENST00000690679.1",
"protein_id": "ENSP00000509380.1",
"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": 1469,
"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": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.350T>G",
"hgvs_p": null,
"transcript": "ENST00000690876.1",
"protein_id": "ENSP00000508955.1",
"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": 5987,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"dbsnp": "rs201085754",
"frequency_reference_population": 0.000012486951,
"hom_count_reference_population": 0,
"allele_count_reference_population": 20,
"gnomad_exomes_af": 0.0000131078,
"gnomad_genomes_af": 0.0000065722,
"gnomad_exomes_ac": 19,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.7171885967254639,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.732,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.827,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.25,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.197,
"phylop100way_prediction": "Pathogenic",
"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": "BS2,PP3,BP5",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 5,
"pathogenic_score": 1,
"criteria": [
"BS2",
"PP3",
"BP5"
],
"verdict": "Likely_benign",
"transcript": "ENST00000402219.8",
"gene_symbol": "SOS1",
"hgnc_id": 11187,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.350T>G",
"hgvs_p": "p.Val117Gly"
}
],
"clinvar_disease": "Cardiovascular phenotype,RASopathy,not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "reviewed by expert panel",
"clinvar_submissions_summary": "US:3 LB:3",
"phenotype_combined": "not specified|RASopathy|Cardiovascular phenotype",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}