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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: 12-42460216-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=42460216&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 2,
"criteria": [
"BP4_Moderate"
],
"effects": [
"missense_variant"
],
"gene_symbol": "PRICKLE1",
"hgnc_id": 17019,
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"inheritance_mode": "AR,AD",
"pathogenic_score": 0,
"score": -2,
"transcript": "NM_153026.3",
"verdict": "Likely_benign"
},
{
"benign_score": 2,
"criteria": [
"BP4_Moderate"
],
"effects": [
"non_coding_transcript_exon_variant"
],
"gene_symbol": "ENSG00000257225",
"hgnc_id": 58444,
"hgvs_c": "n.851G>A",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 0,
"score": -2,
"transcript": "ENST00000547824.1",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_score": -2,
"allele_count_reference_population": 22,
"alphamissense_prediction": null,
"alphamissense_score": 0.0834,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.44,
"chr": "12",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": " 1B, progressive myoclonic,Epilepsy",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.08922281861305237,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5878,
"cdna_start": 2419,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_153026.3",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000345127.9",
"protein_coding": true,
"protein_id": "NP_694571.2",
"strand": false,
"transcript": "NM_153026.3",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5878,
"cdna_start": 2419,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000345127.9",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_153026.3",
"protein_coding": true,
"protein_id": "ENSP00000345064.3",
"strand": false,
"transcript": "ENST00000345127.9",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 2791,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 2,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000547824.1",
"gene_hgnc_id": 58444,
"gene_symbol": "ENSG00000257225",
"hgvs_c": "n.851G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "ENST00000547824.1",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5836,
"cdna_start": 2377,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001144881.2",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001138353.1",
"strand": false,
"transcript": "NM_001144881.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5849,
"cdna_start": 2390,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001144882.2",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001138354.1",
"strand": false,
"transcript": "NM_001144882.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5846,
"cdna_start": 2387,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001144883.2",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001138355.1",
"strand": false,
"transcript": "NM_001144883.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4075,
"cdna_start": 2219,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000445766.7",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000398947.2",
"strand": false,
"transcript": "ENST00000445766.7",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4277,
"cdna_start": 2433,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000455697.6",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000401060.1",
"strand": false,
"transcript": "ENST00000455697.6",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3635,
"cdna_start": 2370,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000548696.6",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000448359.1",
"strand": false,
"transcript": "ENST00000548696.6",
"transcript_support_level": 2
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3311,
"cdna_start": 2375,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000552240.6",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000449819.1",
"strand": false,
"transcript": "ENST00000552240.6",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3341,
"cdna_start": 2390,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000639566.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000492332.1",
"strand": false,
"transcript": "ENST00000639566.1",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5761,
"cdna_start": 2308,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000639589.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000491051.1",
"strand": false,
"transcript": "ENST00000639589.1",
"transcript_support_level": 5
},
{
"aa_alt": "S",
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"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3803,
"cdna_start": 2416,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000639958.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000492644.1",
"strand": false,
"transcript": "ENST00000639958.1",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3778,
"cdna_start": 2387,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000640055.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000492763.1",
"strand": false,
"transcript": "ENST00000640055.1",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4278,
"cdna_start": 2434,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000640132.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000491228.1",
"strand": false,
"transcript": "ENST00000640132.1",
"transcript_support_level": 2
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3674,
"cdna_start": 2708,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000899955.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000570014.1",
"strand": false,
"transcript": "ENST00000899955.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 831,
"aa_ref": "P",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4280,
"cdna_start": 2420,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000899957.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000570016.1",
"strand": false,
"transcript": "ENST00000899957.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 831,
"aa_ref": "P",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3163,
"cdna_start": 2197,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000899959.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000570018.1",
"strand": false,
"transcript": "ENST00000899959.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3398,
"cdna_start": 2432,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000899960.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000570019.1",
"strand": false,
"transcript": "ENST00000899960.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
"aa_start": 697,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3139,
"cdna_start": 2173,
"cds_end": null,
"cds_length": 2496,
"cds_start": 2089,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000899961.1",
"gene_hgnc_id": 17019,
"gene_symbol": "PRICKLE1",
"hgvs_c": "c.2089C>T",
"hgvs_p": "p.Pro697Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000570020.1",
"strand": false,
"transcript": "ENST00000899961.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 831,
"aa_ref": "P",
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