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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: 1-26442821-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=26442821&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 26442821,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000236342.12",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "NM_205861.3",
"protein_id": "NP_995583.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 333,
"cds_start": 271,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 382,
"cdna_end": null,
"cdna_length": 3288,
"mane_select": "ENST00000236342.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000236342.12",
"protein_id": "ENSP00000236342.7",
"transcript_support_level": 1,
"aa_start": 91,
"aa_end": null,
"aa_length": 333,
"cds_start": 271,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 382,
"cdna_end": null,
"cdna_length": 3288,
"mane_select": "NM_205861.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000526219.5",
"protein_id": "ENSP00000434219.1",
"transcript_support_level": 1,
"aa_start": 91,
"aa_end": null,
"aa_length": 294,
"cds_start": 271,
"cds_end": null,
"cds_length": 885,
"cdna_start": 363,
"cdna_end": null,
"cdna_length": 1072,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "n.*72G>C",
"hgvs_p": null,
"transcript": "ENST00000434391.6",
"protein_id": "ENSP00000403529.2",
"transcript_support_level": 1,
"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": 3338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "n.*72G>C",
"hgvs_p": null,
"transcript": "ENST00000434391.6",
"protein_id": "ENSP00000403529.2",
"transcript_support_level": 1,
"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": 3338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000703262.1",
"protein_id": "ENSP00000515247.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 354,
"cds_start": 271,
"cds_end": null,
"cds_length": 1065,
"cdna_start": 374,
"cdna_end": null,
"cdna_length": 2410,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "NM_024887.4",
"protein_id": "NP_079163.2",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 334,
"cds_start": 271,
"cds_end": null,
"cds_length": 1005,
"cdna_start": 382,
"cdna_end": null,
"cdna_length": 3291,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000360009.6",
"protein_id": "ENSP00000353104.2",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 334,
"cds_start": 271,
"cds_end": null,
"cds_length": 1005,
"cdna_start": 348,
"cdna_end": null,
"cdna_length": 3245,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000528557.6",
"protein_id": "ENSP00000515248.1",
"transcript_support_level": 4,
"aa_start": 91,
"aa_end": null,
"aa_length": 333,
"cds_start": 271,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 437,
"cdna_end": null,
"cdna_length": 2777,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "NM_001243564.2",
"protein_id": "NP_001230493.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 299,
"cds_start": 271,
"cds_end": null,
"cds_length": 900,
"cdna_start": 382,
"cdna_end": null,
"cdna_length": 3186,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000525682.6",
"protein_id": "ENSP00000434984.1",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 299,
"cds_start": 271,
"cds_end": null,
"cds_length": 900,
"cdna_start": 364,
"cdna_end": null,
"cdna_length": 1235,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000703198.1",
"protein_id": "ENSP00000515227.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 297,
"cds_start": 271,
"cds_end": null,
"cds_length": 894,
"cdna_start": 361,
"cdna_end": null,
"cdna_length": 1983,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "NM_001243565.2",
"protein_id": "NP_001230494.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 294,
"cds_start": 271,
"cds_end": null,
"cds_length": 885,
"cdna_start": 382,
"cdna_end": null,
"cdna_length": 3171,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000703199.1",
"protein_id": "ENSP00000515228.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 260,
"cds_start": 271,
"cds_end": null,
"cds_length": 783,
"cdna_start": 348,
"cdna_end": null,
"cdna_length": 2039,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000430232.5",
"protein_id": "ENSP00000397584.1",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 215,
"cds_start": 271,
"cds_end": null,
"cds_length": 648,
"cdna_start": 326,
"cdna_end": null,
"cdna_length": 703,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000374185.7",
"protein_id": "ENSP00000363300.3",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 209,
"cds_start": 271,
"cds_end": null,
"cds_length": 630,
"cdna_start": 361,
"cdna_end": null,
"cdna_length": 1148,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000427245.6",
"protein_id": "ENSP00000399177.2",
"transcript_support_level": 5,
"aa_start": 91,
"aa_end": null,
"aa_length": 198,
"cds_start": 271,
"cds_end": null,
"cds_length": 597,
"cdna_start": 387,
"cdna_end": null,
"cdna_length": 868,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000436153.6",
"protein_id": "ENSP00000405604.2",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 172,
"cds_start": 271,
"cds_end": null,
"cds_length": 521,
"cdna_start": 455,
"cdna_end": null,
"cdna_length": 705,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000533087.5",
"protein_id": "ENSP00000436119.1",
"transcript_support_level": 5,
"aa_start": 91,
"aa_end": null,
"aa_length": 164,
"cds_start": 271,
"cds_end": null,
"cds_length": 497,
"cdna_start": 356,
"cdna_end": null,
"cdna_length": 582,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000531312.5",
"protein_id": "ENSP00000436764.1",
"transcript_support_level": 4,
"aa_start": 91,
"aa_end": null,
"aa_length": 129,
"cds_start": 271,
"cds_end": null,
"cds_length": 392,
"cdna_start": 375,
"cdna_end": null,
"cdna_length": 496,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "ENST00000525165.5",
"protein_id": "ENSP00000434185.1",
"transcript_support_level": 2,
"aa_start": 91,
"aa_end": null,
"aa_length": 121,
"cds_start": 271,
"cds_end": null,
"cds_length": 367,
"cdna_start": 477,
"cdna_end": null,
"cdna_length": 573,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "XM_047430849.1",
"protein_id": "XP_047286805.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 334,
"cds_start": 271,
"cds_end": null,
"cds_length": 1005,
"cdna_start": 524,
"cdna_end": null,
"cdna_length": 3433,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DHDDS",
"gene_hgnc_id": 20603,
"hgvs_c": "c.271G>C",
"hgvs_p": "p.Asp91His",
"transcript": "XM_047430850.1",
"protein_id": "XP_047286806.1",
"transcript_support_level": null,
"aa_start": 91,
"aa_end": null,
"aa_length": 334,
"cds_start": 271,
"cds_end": null,
"cds_length": 1005,
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],
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"bayesdelnoaf_score": 0.05,
"bayesdelnoaf_prediction": "Uncertain_significance",
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"phylop100way_prediction": "Pathogenic",
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"acmg_classification": "Uncertain_significance",
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"acmg_by_gene": [
{
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"verdict": "Uncertain_significance",
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{
"score": 2,
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],
"clinvar_disease": "Retinitis pigmentosa 59",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Retinitis pigmentosa 59",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}