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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: 19-50415559-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=50415559&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 1,
"criteria": [
"BP4"
],
"effects": [
"missense_variant"
],
"gene_symbol": "POLD1",
"hgnc_id": 9175,
"hgvs_c": "c.2764G>A",
"hgvs_p": "p.Gly922Ser",
"inheritance_mode": "AD,AR",
"pathogenic_score": 0,
"score": -1,
"transcript": "NM_001308632.1",
"verdict": "Likely_benign"
},
{
"benign_score": 1,
"criteria": [
"PM2",
"BP4"
],
"effects": [
"upstream_gene_variant"
],
"gene_symbol": "ENSG00000142539",
"hgnc_id": null,
"hgvs_c": "c.-241G>A",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 2,
"score": 1,
"transcript": "ENST00000599632.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4",
"acmg_score": -1,
"allele_count_reference_population": 10,
"alphamissense_prediction": null,
"alphamissense_score": 0.1389,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.43,
"chr": "19",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": " 10, susceptibility to,Colorectal cancer,Hereditary cancer-predisposing syndrome,Immunodeficiency 120,Mandibular hypoplasia-deafness-progeroid syndrome,not provided",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:3 LB:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.3530973196029663,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3436,
"cdna_start": 2731,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_002691.4",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000440232.7",
"protein_coding": true,
"protein_id": "NP_002682.2",
"strand": true,
"transcript": "NM_002691.4",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3436,
"cdna_start": 2731,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000440232.7",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_002691.4",
"protein_coding": true,
"protein_id": "ENSP00000406046.1",
"strand": true,
"transcript": "ENST00000440232.7",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "G",
"aa_start": 922,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3514,
"cdna_start": 2809,
"cds_end": null,
"cds_length": 3402,
"cds_start": 2764,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000595904.6",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2764G>A",
"hgvs_p": "p.Gly922Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000472445.1",
"strand": true,
"transcript": "ENST00000595904.6",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3467,
"cdna_start": 2758,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000599857.7",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000473052.1",
"strand": true,
"transcript": "ENST00000599857.7",
"transcript_support_level": 1
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1143,
"aa_ref": "G",
"aa_start": 932,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3579,
"cdna_start": 2876,
"cds_end": null,
"cds_length": 3432,
"cds_start": 2794,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000935846.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2794G>A",
"hgvs_p": "p.Gly932Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605905.1",
"strand": true,
"transcript": "ENST00000935846.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "G",
"aa_start": 922,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3473,
"cdna_start": 2764,
"cds_end": null,
"cds_length": 3402,
"cds_start": 2764,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001308632.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2764G>A",
"hgvs_p": "p.Gly922Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001295561.1",
"strand": true,
"transcript": "NM_001308632.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "G",
"aa_start": 922,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3514,
"cdna_start": 2809,
"cds_end": null,
"cds_length": 3402,
"cds_start": 2764,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000869782.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2764G>A",
"hgvs_p": "p.Gly922Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000539841.1",
"strand": true,
"transcript": "ENST00000869782.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "G",
"aa_start": 922,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3729,
"cdna_start": 3024,
"cds_end": null,
"cds_length": 3402,
"cds_start": 2764,
"consequences": [
"missense_variant"
],
"exon_count": 29,
"exon_rank": 23,
"exon_rank_end": null,
"feature": "ENST00000969650.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2764G>A",
"hgvs_p": "p.Gly922Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000639709.1",
"strand": true,
"transcript": "ENST00000969650.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1109,
"aa_ref": "G",
"aa_start": 898,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3370,
"cdna_start": 2692,
"cds_end": null,
"cds_length": 3330,
"cds_start": 2692,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "ENST00000644560.2",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2692G>A",
"hgvs_p": "p.Gly898Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000495618.2",
"strand": true,
"transcript": "ENST00000644560.2",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3467,
"cdna_start": 2758,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001256849.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001243778.1",
"strand": true,
"transcript": "NM_001256849.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3581,
"cdna_start": 2876,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "NM_001438212.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425141.1",
"strand": true,
"transcript": "NM_001438212.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3562,
"cdna_start": 2857,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "NM_001438213.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425142.1",
"strand": true,
"transcript": "NM_001438213.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3703,
"cdna_start": 3065,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000593887.2",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000472607.2",
"strand": true,
"transcript": "ENST00000593887.2",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3524,
"cdna_start": 2862,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "ENST00000601098.6",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000472600.2",
"strand": true,
"transcript": "ENST00000601098.6",
"transcript_support_level": 3
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3438,
"cdna_start": 2750,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000687454.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000510052.1",
"strand": true,
"transcript": "ENST00000687454.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3552,
"cdna_start": 2845,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "ENST00000869780.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000539839.1",
"strand": true,
"transcript": "ENST00000869780.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 1107,
"aa_ref": "G",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3627,
"cdna_start": 2923,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 29,
"exon_rank": 23,
"exon_rank_end": null,
"feature": "ENST00000869783.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000539842.1",
"strand": true,
"transcript": "ENST00000869783.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4422,
"cdna_start": 3722,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "ENST00000935843.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605902.1",
"strand": true,
"transcript": "ENST00000935843.1",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3643,
"cdna_start": 2938,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "ENST00000935844.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605903.1",
"strand": true,
"transcript": "ENST00000935844.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1107,
"aa_ref": "G",
"aa_start": 896,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3583,
"cdna_start": 2876,
"cds_end": null,
"cds_length": 3324,
"cds_start": 2686,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 22,
"exon_rank_end": null,
"feature": "ENST00000935847.1",
"gene_hgnc_id": 9175,
"gene_symbol": "POLD1",
"hgvs_c": "c.2686G>A",
"hgvs_p": "p.Gly896Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605906.1",
"strand": true,
"transcript": "ENST00000935847.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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