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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: 22-31837089-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=31837089&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 5,
"criteria": [
"BP4",
"BS2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "DEPDC5",
"hgnc_id": 18423,
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -5,
"transcript": "NM_001242896.3",
"verdict": "Likely_benign"
},
{
"benign_score": 1,
"criteria": [
"BP4"
],
"effects": [
"intron_variant"
],
"gene_symbol": "ENSG00000285404",
"hgnc_id": null,
"hgvs_c": "c.1786+17864G>A",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 0,
"score": -1,
"transcript": "ENST00000646701.1",
"verdict": "Likely_benign"
},
{
"benign_score": 1,
"criteria": [
"BP4"
],
"effects": [
"upstream_gene_variant"
],
"gene_symbol": "RNU6-201P",
"hgnc_id": 47164,
"hgvs_c": "n.-149G>A",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 0,
"score": -1,
"transcript": "ENST00000517100.1",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4,BS2",
"acmg_score": -5,
"allele_count_reference_population": 54,
"alphamissense_prediction": null,
"alphamissense_score": 0.0982,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Uncertain_significance",
"bayesdelnoaf_score": -0.07,
"chr": "22",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "Familial focal epilepsy with variable foci",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.3686903715133667,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1603,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6554,
"cdna_start": 2494,
"cds_end": null,
"cds_length": 4812,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "NM_001242896.3",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000651528.2",
"protein_coding": true,
"protein_id": "NP_001229825.1",
"strand": true,
"transcript": "NM_001242896.3",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1603,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 6554,
"cdna_start": 2494,
"cds_end": null,
"cds_length": 4812,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000651528.2",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001242896.3",
"protein_coding": true,
"protein_id": "ENSP00000498382.1",
"strand": true,
"transcript": "ENST00000651528.2",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1603,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5390,
"cdna_start": 2374,
"cds_end": null,
"cds_length": 4812,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000382112.8",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000371546.4",
"strand": true,
"transcript": "ENST00000382112.8",
"transcript_support_level": 1
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1575,
"aa_ref": "R",
"aa_start": 735,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5331,
"cdna_start": 2306,
"cds_end": null,
"cds_length": 4728,
"cds_start": 2204,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 25,
"exon_rank_end": null,
"feature": "ENST00000433147.2",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2204G>A",
"hgvs_p": "p.Arg735His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000410544.2",
"strand": true,
"transcript": "ENST00000433147.2",
"transcript_support_level": 1
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1572,
"aa_ref": "R",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5319,
"cdna_start": 2344,
"cds_end": null,
"cds_length": 4719,
"cds_start": 2261,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000400248.7",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2261G>A",
"hgvs_p": "p.Arg754His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000383107.1",
"strand": true,
"transcript": "ENST00000400248.7",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 600,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1914,
"cdna_start": null,
"cds_end": null,
"cds_length": 1803,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000646701.1",
"gene_hgnc_id": null,
"gene_symbol": "ENSG00000285404",
"hgvs_c": "c.1786+17864G>A",
"hgvs_p": null,
"intron_rank": 20,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000496158.1",
"strand": true,
"transcript": "ENST00000646701.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 5725,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 41,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000400246.7",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "n.2054G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000383105.3",
"strand": true,
"transcript": "ENST00000400246.7",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3256,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 19,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000448753.6",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "n.344G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000402173.1",
"strand": true,
"transcript": "ENST00000448753.6",
"transcript_support_level": 1
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1611,
"aa_ref": "R",
"aa_start": 771,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5532,
"cdna_start": 2491,
"cds_end": null,
"cds_length": 4836,
"cds_start": 2312,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000915004.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2312G>A",
"hgvs_p": "p.Arg771His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000585063.1",
"strand": true,
"transcript": "ENST00000915004.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1603,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6437,
"cdna_start": 2377,
"cds_end": null,
"cds_length": 4812,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "NM_001364318.2",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001351247.1",
"strand": true,
"transcript": "NM_001364318.2",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1594,
"aa_ref": "R",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6410,
"cdna_start": 2350,
"cds_end": null,
"cds_length": 4785,
"cds_start": 2261,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "NM_001136029.4",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2261G>A",
"hgvs_p": "p.Arg754His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001129501.1",
"strand": true,
"transcript": "NM_001136029.4",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1594,
"aa_ref": "R",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5450,
"cdna_start": 2418,
"cds_end": null,
"cds_length": 4785,
"cds_start": 2261,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000645711.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2261G>A",
"hgvs_p": "p.Arg754His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000493489.1",
"strand": true,
"transcript": "ENST00000645711.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1594,
"aa_ref": "R",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5546,
"cdna_start": 2496,
"cds_end": null,
"cds_length": 4785,
"cds_start": 2261,
"consequences": [
"missense_variant"
],
"exon_count": 43,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000915008.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2261G>A",
"hgvs_p": "p.Arg754His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000585067.1",
"strand": true,
"transcript": "ENST00000915008.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1589,
"aa_ref": "R",
"aa_start": 771,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5010,
"cdna_start": 2319,
"cds_end": null,
"cds_length": 4770,
"cds_start": 2312,
"consequences": [
"missense_variant"
],
"exon_count": 41,
"exon_rank": 25,
"exon_rank_end": null,
"feature": "ENST00000645407.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2312G>A",
"hgvs_p": "p.Arg771His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000496252.1",
"strand": true,
"transcript": "ENST00000645407.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1581,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5353,
"cdna_start": 2377,
"cds_end": null,
"cds_length": 4746,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "NM_001363852.2",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001350781.1",
"strand": true,
"transcript": "NM_001363852.2",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1581,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6488,
"cdna_start": 2494,
"cds_end": null,
"cds_length": 4746,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "NM_001364320.2",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001351249.1",
"strand": true,
"transcript": "NM_001364320.2",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1581,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5350,
"cdna_start": 2380,
"cds_end": null,
"cds_length": 4746,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000400249.7",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000383108.3",
"strand": true,
"transcript": "ENST00000400249.7",
"transcript_support_level": 5
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1581,
"aa_ref": "R",
"aa_start": 763,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5383,
"cdna_start": 2433,
"cds_end": null,
"cds_length": 4746,
"cds_start": 2288,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 26,
"exon_rank_end": null,
"feature": "ENST00000644331.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2288G>A",
"hgvs_p": "p.Arg763His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000494406.1",
"strand": true,
"transcript": "ENST00000644331.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1575,
"aa_ref": "R",
"aa_start": 735,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5448,
"cdna_start": 2406,
"cds_end": null,
"cds_length": 4728,
"cds_start": 2204,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 25,
"exon_rank_end": null,
"feature": "NM_001369901.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2204G>A",
"hgvs_p": "p.Arg735His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001356830.1",
"strand": true,
"transcript": "NM_001369901.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1575,
"aa_ref": "R",
"aa_start": 735,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5335,
"cdna_start": 2293,
"cds_end": null,
"cds_length": 4728,
"cds_start": 2204,
"consequences": [
"missense_variant"
],
"exon_count": 42,
"exon_rank": 25,
"exon_rank_end": null,
"feature": "NM_001369902.1",
"gene_hgnc_id": 18423,
"gene_symbol": "DEPDC5",
"hgvs_c": "c.2204G>A",
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{
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{
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],
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]
}