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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: 6-35459406-CCT-TCC (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=35459406&ref=CCT&alt=TCC&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [],
"effects": [
"missense_variant"
],
"gene_symbol": "FANCE",
"hgnc_id": 3586,
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": 0,
"transcript": "NM_021922.3",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_score": 0,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "TCC",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "6",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 536,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2576,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1611,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_021922.3",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000229769.3",
"protein_coding": true,
"protein_id": "NP_068741.1",
"strand": true,
"transcript": "NM_021922.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 536,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2576,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1611,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000229769.3",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_021922.3",
"protein_coding": true,
"protein_id": "ENSP00000229769.2",
"strand": true,
"transcript": "ENST00000229769.3",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 537,
"aa_ref": "P",
"aa_start": 398,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2570,
"cdna_start": 1394,
"cds_end": null,
"cds_length": 1614,
"cds_start": 1192,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000854656.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1192_1194delCCTinsTCC",
"hgvs_p": "p.Pro398Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000524715.1",
"strand": true,
"transcript": "ENST00000854656.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 529,
"aa_ref": "P",
"aa_start": 390,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2543,
"cdna_start": 1364,
"cds_end": null,
"cds_length": 1590,
"cds_start": 1168,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000854658.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1168_1170delCCTinsTCC",
"hgvs_p": "p.Pro390Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000524717.1",
"strand": true,
"transcript": "ENST00000854658.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 527,
"aa_ref": "P",
"aa_start": 388,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2569,
"cdna_start": 1388,
"cds_end": null,
"cds_length": 1584,
"cds_start": 1162,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934267.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1162_1164delCCTinsTCC",
"hgvs_p": "p.Pro388Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604326.1",
"strand": true,
"transcript": "ENST00000934267.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 521,
"aa_ref": "P",
"aa_start": 382,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2541,
"cdna_start": 1362,
"cds_end": null,
"cds_length": 1566,
"cds_start": 1144,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934268.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1144_1146delCCTinsTCC",
"hgvs_p": "p.Pro382Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604327.1",
"strand": true,
"transcript": "ENST00000934268.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 514,
"aa_ref": "P",
"aa_start": 375,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2508,
"cdna_start": 1327,
"cds_end": null,
"cds_length": 1545,
"cds_start": 1123,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934271.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1123_1125delCCTinsTCC",
"hgvs_p": "p.Pro375Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604330.1",
"strand": true,
"transcript": "ENST00000934271.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 514,
"aa_ref": "P",
"aa_start": 375,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2511,
"cdna_start": 1337,
"cds_end": null,
"cds_length": 1545,
"cds_start": 1123,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000962963.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1123_1125delCCTinsTCC",
"hgvs_p": "p.Pro375Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000633022.1",
"strand": true,
"transcript": "ENST00000962963.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 513,
"aa_ref": "P",
"aa_start": 374,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2496,
"cdna_start": 1313,
"cds_end": null,
"cds_length": 1542,
"cds_start": 1120,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000854657.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1120_1122delCCTinsTCC",
"hgvs_p": "p.Pro374Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000524716.1",
"strand": true,
"transcript": "ENST00000854657.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 509,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2476,
"cdna_start": 1385,
"cds_end": null,
"cds_length": 1530,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934272.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604331.1",
"strand": true,
"transcript": "ENST00000934272.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 506,
"aa_ref": "P",
"aa_start": 367,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2510,
"cdna_start": 1327,
"cds_end": null,
"cds_length": 1521,
"cds_start": 1099,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934266.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1099_1101delCCTinsTCC",
"hgvs_p": "p.Pro367Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604325.1",
"strand": true,
"transcript": "ENST00000934266.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 504,
"aa_ref": "P",
"aa_start": 365,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2460,
"cdna_start": 1286,
"cds_end": null,
"cds_length": 1515,
"cds_start": 1093,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934273.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1093_1095delCCTinsTCC",
"hgvs_p": "p.Pro365Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604332.1",
"strand": true,
"transcript": "ENST00000934273.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 494,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2460,
"cdna_start": 1405,
"cds_end": null,
"cds_length": 1485,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934269.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604328.1",
"strand": true,
"transcript": "ENST00000934269.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 487,
"aa_ref": "P",
"aa_start": 390,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2427,
"cdna_start": 1370,
"cds_end": null,
"cds_length": 1464,
"cds_start": 1168,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000962964.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1168_1170delCCTinsTCC",
"hgvs_p": "p.Pro390Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000633023.1",
"strand": true,
"transcript": "ENST00000962964.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 471,
"aa_ref": "P",
"aa_start": 374,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2388,
"cdna_start": 1331,
"cds_end": null,
"cds_length": 1416,
"cds_start": 1120,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000934270.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1120_1122delCCTinsTCC",
"hgvs_p": "p.Pro374Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000604329.1",
"strand": true,
"transcript": "ENST00000934270.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 451,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2383,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1356,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001410876.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001397805.1",
"strand": true,
"transcript": "NM_001410876.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 451,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2137,
"cdna_start": 1189,
"cds_end": null,
"cds_length": 1356,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000696264.1",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000512511.1",
"strand": true,
"transcript": "ENST00000696264.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 529,
"aa_ref": "P",
"aa_start": 390,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2555,
"cdna_start": 1376,
"cds_end": null,
"cds_length": 1590,
"cds_start": 1168,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_005248885.3",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1168_1170delCCTinsTCC",
"hgvs_p": "p.Pro390Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005248942.1",
"strand": true,
"transcript": "XM_005248885.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 513,
"aa_ref": "P",
"aa_start": 374,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2507,
"cdna_start": 1328,
"cds_end": null,
"cds_length": 1542,
"cds_start": 1120,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_005248886.3",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1120_1122delCCTinsTCC",
"hgvs_p": "p.Pro374Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005248943.1",
"strand": true,
"transcript": "XM_005248886.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 494,
"aa_ref": "P",
"aa_start": 397,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2450,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1485,
"cds_start": 1189,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_005248887.3",
"gene_hgnc_id": 3586,
"gene_symbol": "FANCE",
"hgvs_c": "c.1189_1191delCCTinsTCC",
"hgvs_p": "p.Pro397Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005248944.1",
"strand": true,
"transcript": "XM_005248887.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 471,
"aa_ref": "P",
"aa_start": 374,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2381,
"cdna_start": 1328,
"cds_end": null,
"cds_length": 1416,
"cds_start": 1120,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047418300.1",
"gene_hgnc_id": 3586,
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