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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: 6-152219144-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=152219144&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 4,
"criteria": [
"BP4_Strong"
],
"effects": [
"missense_variant"
],
"gene_symbol": "SYNE1",
"hgnc_id": 17089,
"hgvs_c": "c.21903T>A",
"hgvs_p": "p.Phe7301Leu",
"inheritance_mode": "AD,AR",
"pathogenic_score": 0,
"score": -4,
"transcript": "NM_182961.4",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_score": -4,
"allele_count_reference_population": 24,
"alphamissense_prediction": null,
"alphamissense_score": 0.273,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.45,
"chr": "6",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.050795942544937134,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8797,
"aa_ref": "F",
"aa_start": 7301,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27708,
"cdna_start": 22468,
"cds_end": null,
"cds_length": 26394,
"cds_start": 21903,
"consequences": [
"missense_variant"
],
"exon_count": 146,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "NM_182961.4",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21903T>A",
"hgvs_p": "p.Phe7301Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000367255.10",
"protein_coding": true,
"protein_id": "NP_892006.3",
"strand": false,
"transcript": "NM_182961.4",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8797,
"aa_ref": "F",
"aa_start": 7301,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 27708,
"cdna_start": 22468,
"cds_end": null,
"cds_length": 26394,
"cds_start": 21903,
"consequences": [
"missense_variant"
],
"exon_count": 146,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "ENST00000367255.10",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21903T>A",
"hgvs_p": "p.Phe7301Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_182961.4",
"protein_coding": true,
"protein_id": "ENSP00000356224.5",
"strand": false,
"transcript": "ENST00000367255.10",
"transcript_support_level": 1
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8749,
"aa_ref": "F",
"aa_start": 7230,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27475,
"cdna_start": 22166,
"cds_end": null,
"cds_length": 26250,
"cds_start": 21690,
"consequences": [
"missense_variant"
],
"exon_count": 146,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "ENST00000423061.6",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21690T>A",
"hgvs_p": "p.Phe7230Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000396024.1",
"strand": false,
"transcript": "ENST00000423061.6",
"transcript_support_level": 1
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 1654,
"aa_ref": "F",
"aa_start": 223,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5837,
"cdna_start": 669,
"cds_end": null,
"cds_length": 4965,
"cds_start": 669,
"consequences": [
"missense_variant"
],
"exon_count": 31,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000367251.7",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.669T>A",
"hgvs_p": "p.Phe223Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000356220.3",
"strand": false,
"transcript": "ENST00000367251.7",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 10742,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 61,
"exon_rank": 35,
"exon_rank_end": null,
"feature": "ENST00000367256.9",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "n.5595T>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000367256.9",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 10634,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 59,
"exon_rank": 33,
"exon_rank_end": null,
"feature": "ENST00000409694.6",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "n.5487T>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000409694.6",
"transcript_support_level": 1
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8749,
"aa_ref": "F",
"aa_start": 7230,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27475,
"cdna_start": 22166,
"cds_end": null,
"cds_length": 26250,
"cds_start": 21690,
"consequences": [
"missense_variant"
],
"exon_count": 146,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "NM_033071.5",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21690T>A",
"hgvs_p": "p.Phe7230Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_149062.2",
"strand": false,
"transcript": "NM_033071.5",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8846,
"aa_ref": "F",
"aa_start": 7313,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27766,
"cdna_start": 22415,
"cds_end": null,
"cds_length": 26541,
"cds_start": 21939,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_006715407.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21939T>A",
"hgvs_p": "p.Phe7313Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715470.1",
"strand": false,
"transcript": "XM_006715407.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8846,
"aa_ref": "F",
"aa_start": 7313,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27855,
"cdna_start": 22504,
"cds_end": null,
"cds_length": 26541,
"cds_start": 21939,
"consequences": [
"missense_variant"
],
"exon_count": 149,
"exon_rank": 121,
"exon_rank_end": null,
"feature": "XM_017010608.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21939T>A",
"hgvs_p": "p.Phe7313Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866097.1",
"strand": false,
"transcript": "XM_017010608.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8846,
"aa_ref": "F",
"aa_start": 7313,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27687,
"cdna_start": 22336,
"cds_end": null,
"cds_length": 26541,
"cds_start": 21939,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_017010609.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21939T>A",
"hgvs_p": "p.Phe7313Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866098.1",
"strand": false,
"transcript": "XM_017010609.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8845,
"aa_ref": "F",
"aa_start": 7312,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27763,
"cdna_start": 22412,
"cds_end": null,
"cds_length": 26538,
"cds_start": 21936,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_011535641.3",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21936T>A",
"hgvs_p": "p.Phe7312Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011533943.1",
"strand": false,
"transcript": "XM_011535641.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8842,
"aa_ref": "F",
"aa_start": 7309,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27754,
"cdna_start": 22403,
"cds_end": null,
"cds_length": 26529,
"cds_start": 21927,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_006715408.3",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21927T>A",
"hgvs_p": "p.Phe7309Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715471.1",
"strand": false,
"transcript": "XM_006715408.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
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"aa_length": 8841,
"aa_ref": "F",
"aa_start": 7308,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27751,
"cdna_start": 22400,
"cds_end": null,
"cds_length": 26526,
"cds_start": 21924,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_011535642.3",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21924T>A",
"hgvs_p": "p.Phe7308Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011533944.1",
"strand": false,
"transcript": "XM_011535642.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8839,
"aa_ref": "F",
"aa_start": 7306,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27745,
"cdna_start": 22394,
"cds_end": null,
"cds_length": 26520,
"cds_start": 21918,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "XM_006715409.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21918T>A",
"hgvs_p": "p.Phe7306Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715472.1",
"strand": false,
"transcript": "XM_006715409.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8839,
"aa_ref": "F",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27666,
"cdna_start": 22315,
"cds_end": null,
"cds_length": 26520,
"cds_start": 21918,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "XM_017010610.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21918T>A",
"hgvs_p": "p.Phe7306Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866099.1",
"strand": false,
"transcript": "XM_017010610.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8839,
"aa_ref": "F",
"aa_start": 7306,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27834,
"cdna_start": 22483,
"cds_end": null,
"cds_length": 26520,
"cds_start": 21918,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_047418501.1",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21918T>A",
"hgvs_p": "p.Phe7306Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047274457.1",
"strand": false,
"transcript": "XM_047418501.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8837,
"aa_ref": "F",
"aa_start": 7304,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27387,
"cdna_start": 22036,
"cds_end": null,
"cds_length": 26514,
"cds_start": 21912,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "XM_017010611.3",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21912T>A",
"hgvs_p": "p.Phe7304Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866100.1",
"strand": false,
"transcript": "XM_017010611.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
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"aa_ref": "F",
"aa_start": 7313,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27724,
"cdna_start": 22415,
"cds_end": null,
"cds_length": 26499,
"cds_start": 21939,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_006715410.3",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21939T>A",
"hgvs_p": "p.Phe7313Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715473.1",
"strand": false,
"transcript": "XM_006715410.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
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"aa_length": 8831,
"aa_ref": "F",
"aa_start": 7312,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27721,
"cdna_start": 22412,
"cds_end": null,
"cds_length": 26496,
"cds_start": 21936,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_047418502.1",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21936T>A",
"hgvs_p": "p.Phe7312Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047274458.1",
"strand": false,
"transcript": "XM_047418502.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8829,
"aa_ref": "F",
"aa_start": 7296,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27715,
"cdna_start": 22364,
"cds_end": null,
"cds_length": 26490,
"cds_start": 21888,
"consequences": [
"missense_variant"
],
"exon_count": 147,
"exon_rank": 119,
"exon_rank_end": null,
"feature": "XM_006715411.2",
"gene_hgnc_id": 17089,
"gene_symbol": "SYNE1",
"hgvs_c": "c.21888T>A",
"hgvs_p": "p.Phe7296Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715474.1",
"strand": false,
"transcript": "XM_006715411.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 8829,
"aa_ref": "F",
"aa_start": 7296,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 27804,
"cdna_start": 22453,
"cds_end": null,
"cds_length": 26490,
"cds_start": 21888,
"consequences": [
"missense_variant"
],
"exon_count": 148,
"exon_rank": 120,
"exon_rank_end": null,
"feature": "XM_047418503.1",
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