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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: 2-174436190-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=174436190&ref=C&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": "GPR155",
"hgnc_id": 22951,
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -4,
"transcript": "NM_152529.7",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_score": -4,
"allele_count_reference_population": 34,
"alphamissense_prediction": null,
"alphamissense_score": 0.0669,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.81,
"chr": "2",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "not specified",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.03007909655570984,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7346,
"cdna_start": 2727,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "NM_152529.7",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000392552.7",
"protein_coding": true,
"protein_id": "NP_689742.4",
"strand": false,
"transcript": "NM_152529.7",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 7346,
"cdna_start": 2727,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000392552.7",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_152529.7",
"protein_coding": true,
"protein_id": "ENSP00000376335.2",
"strand": false,
"transcript": "ENST00000392552.7",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3930,
"cdna_start": 2884,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000295500.8",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000295500.4",
"strand": false,
"transcript": "ENST00000295500.8",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4876,
"cdna_start": 2838,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000392551.6",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000376334.2",
"strand": false,
"transcript": "ENST00000392551.6",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 842,
"aa_ref": "A",
"aa_start": 819,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7321,
"cdna_start": 2702,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000614352.4",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000481104.1",
"strand": false,
"transcript": "ENST00000614352.4",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7495,
"cdna_start": 2876,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_001033045.4",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001028217.1",
"strand": false,
"transcript": "NM_001033045.4",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7392,
"cdna_start": 2773,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_001267050.2",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001253979.1",
"strand": false,
"transcript": "NM_001267050.2",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3585,
"cdna_start": 2860,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000886492.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000556551.1",
"strand": false,
"transcript": "ENST00000886492.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3507,
"cdna_start": 2770,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000932232.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000602291.1",
"strand": false,
"transcript": "ENST00000932232.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3625,
"cdna_start": 2888,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 18,
"exon_rank_end": null,
"feature": "ENST00000932233.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000602292.1",
"strand": false,
"transcript": "ENST00000932233.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4453,
"cdna_start": 3072,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000949639.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619698.1",
"strand": false,
"transcript": "ENST00000949639.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 870,
"aa_ref": "A",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3623,
"cdna_start": 2923,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000949644.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2539G>A",
"hgvs_p": "p.Ala847Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619703.1",
"strand": false,
"transcript": "ENST00000949644.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
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"aa_length": 856,
"aa_ref": "A",
"aa_start": 833,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3419,
"cdna_start": 2719,
"cds_end": null,
"cds_length": 2571,
"cds_start": 2497,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000949645.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2497G>A",
"hgvs_p": "p.Ala833Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619704.1",
"strand": false,
"transcript": "ENST00000949645.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 842,
"aa_ref": "A",
"aa_start": 819,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7262,
"cdna_start": 2643,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "NM_001267051.2",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001253980.1",
"strand": false,
"transcript": "NM_001267051.2",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 842,
"aa_ref": "A",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3529,
"cdna_start": 2792,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000886493.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000556552.1",
"strand": false,
"transcript": "ENST00000886493.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 842,
"aa_ref": "A",
"aa_start": 819,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3462,
"cdna_start": 2762,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000949640.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619699.1",
"strand": false,
"transcript": "ENST00000949640.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 842,
"aa_ref": "A",
"aa_start": 819,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3488,
"cdna_start": 2788,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000949641.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619700.1",
"strand": false,
"transcript": "ENST00000949641.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
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"aa_ref": "A",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3454,
"cdna_start": 2754,
"cds_end": null,
"cds_length": 2529,
"cds_start": 2455,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000949642.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2455G>A",
"hgvs_p": "p.Ala819Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619701.1",
"strand": false,
"transcript": "ENST00000949642.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 835,
"aa_ref": "A",
"aa_start": 812,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4087,
"cdna_start": 2671,
"cds_end": null,
"cds_length": 2508,
"cds_start": 2434,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000886491.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2434G>A",
"hgvs_p": "p.Ala812Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000556550.1",
"strand": false,
"transcript": "ENST00000886491.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 835,
"aa_ref": "A",
"aa_start": 812,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3536,
"cdna_start": 2826,
"cds_end": null,
"cds_length": 2508,
"cds_start": 2434,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000949643.1",
"gene_hgnc_id": 22951,
"gene_symbol": "GPR155",
"hgvs_c": "c.2434G>A",
"hgvs_p": "p.Ala812Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000619702.1",
"strand": false,
"transcript": "ENST00000949643.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 713,
"aa_ref": "A",
"aa_start": 690,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2970,
"cdna_start": 2270,
"cds_end": null,
"cds_length": 2142,
"cds_start": 2068,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 12,
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}