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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: 1-51772132-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=51772132&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 2,
"criteria": [
"BP4_Moderate"
],
"effects": [
"missense_variant"
],
"gene_symbol": "OSBPL9",
"hgnc_id": 16386,
"hgvs_c": "c.1055A>G",
"hgvs_p": "p.Asp352Gly",
"inheritance_mode": "AR,AD",
"pathogenic_score": 0,
"score": -2,
"transcript": "NM_001416292.1",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_score": -2,
"allele_count_reference_population": 16,
"alphamissense_prediction": null,
"alphamissense_score": 0.1723,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.28,
"chr": "1",
"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": 0.13270515203475952,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 736,
"aa_ref": "D",
"aa_start": 334,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3660,
"cdna_start": 1020,
"cds_end": null,
"cds_length": 2211,
"cds_start": 1001,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_024586.6",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1001A>G",
"hgvs_p": "p.Asp334Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000428468.6",
"protein_coding": true,
"protein_id": "NP_078862.4",
"strand": true,
"transcript": "NM_024586.6",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 736,
"aa_ref": "D",
"aa_start": 334,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3660,
"cdna_start": 1020,
"cds_end": null,
"cds_length": 2211,
"cds_start": 1001,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000428468.6",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1001A>G",
"hgvs_p": "p.Asp334Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_024586.6",
"protein_coding": true,
"protein_id": "ENSP00000407168.1",
"strand": true,
"transcript": "ENST00000428468.6",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 719,
"aa_ref": "D",
"aa_start": 317,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2842,
"cdna_start": 952,
"cds_end": null,
"cds_length": 2160,
"cds_start": 950,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000453295.5",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asp317Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000413263.1",
"strand": true,
"transcript": "ENST00000453295.5",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 626,
"aa_ref": "D",
"aa_start": 224,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2721,
"cdna_start": 831,
"cds_end": null,
"cds_length": 1881,
"cds_start": 671,
"consequences": [
"missense_variant"
],
"exon_count": 20,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000361556.9",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.671A>G",
"hgvs_p": "p.Asp224Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000354970.5",
"strand": true,
"transcript": "ENST00000361556.9",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 558,
"aa_ref": "D",
"aa_start": 156,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2755,
"cdna_start": 865,
"cds_end": null,
"cds_length": 1677,
"cds_start": 467,
"consequences": [
"missense_variant"
],
"exon_count": 20,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000462759.5",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.467A>G",
"hgvs_p": "p.Asp156Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000433279.1",
"strand": true,
"transcript": "ENST00000462759.5",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 755,
"aa_ref": "D",
"aa_start": 334,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2899,
"cdna_start": 1023,
"cds_end": null,
"cds_length": 2268,
"cds_start": 1001,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000930350.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1001A>G",
"hgvs_p": "p.Asp334Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000600409.1",
"strand": true,
"transcript": "ENST00000930350.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 754,
"aa_ref": "D",
"aa_start": 352,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3372,
"cdna_start": 1553,
"cds_end": null,
"cds_length": 2265,
"cds_start": 1055,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "NM_001416292.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1055A>G",
"hgvs_p": "p.Asp352Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001403221.1",
"strand": true,
"transcript": "NM_001416292.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 754,
"aa_ref": "D",
"aa_start": 352,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3514,
"cdna_start": 1695,
"cds_end": null,
"cds_length": 2265,
"cds_start": 1055,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "NM_001416293.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1055A>G",
"hgvs_p": "p.Asp352Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001403222.1",
"strand": true,
"transcript": "NM_001416293.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 754,
"aa_ref": "D",
"aa_start": 352,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3629,
"cdna_start": 1810,
"cds_end": null,
"cds_length": 2265,
"cds_start": 1055,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_001416294.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1055A>G",
"hgvs_p": "p.Asp352Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001403223.1",
"strand": true,
"transcript": "NM_001416294.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 746,
"aa_ref": "D",
"aa_start": 344,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3690,
"cdna_start": 1050,
"cds_end": null,
"cds_length": 2241,
"cds_start": 1031,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_148909.4",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1031A>G",
"hgvs_p": "p.Asp344Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_683707.3",
"strand": true,
"transcript": "NM_148909.4",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 746,
"aa_ref": "D",
"aa_start": 344,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2940,
"cdna_start": 1050,
"cds_end": null,
"cds_length": 2241,
"cds_start": 1031,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000447887.5",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1031A>G",
"hgvs_p": "p.Asp344Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000412733.1",
"strand": true,
"transcript": "ENST00000447887.5",
"transcript_support_level": 2
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 744,
"aa_ref": "D",
"aa_start": 342,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2863,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2235,
"cds_start": 1025,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000888375.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1025A>G",
"hgvs_p": "p.Asp342Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558434.1",
"strand": true,
"transcript": "ENST00000888375.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 741,
"aa_ref": "D",
"aa_start": 339,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3333,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 2226,
"cds_start": 1016,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "NM_001416295.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1016A>G",
"hgvs_p": "p.Asp339Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001403224.1",
"strand": true,
"transcript": "NM_001416295.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 734,
"aa_ref": "D",
"aa_start": 334,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2835,
"cdna_start": 1023,
"cds_end": null,
"cds_length": 2205,
"cds_start": 1001,
"consequences": [
"missense_variant"
],
"exon_count": 24,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000888374.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.1001A>G",
"hgvs_p": "p.Asp334Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558433.1",
"strand": true,
"transcript": "ENST00000888374.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 723,
"aa_ref": "D",
"aa_start": 321,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3621,
"cdna_start": 981,
"cds_end": null,
"cds_length": 2172,
"cds_start": 962,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_148908.4",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.962A>G",
"hgvs_p": "p.Asp321Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_683706.3",
"strand": true,
"transcript": "NM_148908.4",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 723,
"aa_ref": "D",
"aa_start": 321,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3352,
"cdna_start": 1462,
"cds_end": null,
"cds_length": 2172,
"cds_start": 962,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000371714.5",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.962A>G",
"hgvs_p": "p.Asp321Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000360779.1",
"strand": true,
"transcript": "ENST00000371714.5",
"transcript_support_level": 2
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 719,
"aa_ref": "D",
"aa_start": 317,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3609,
"cdna_start": 969,
"cds_end": null,
"cds_length": 2160,
"cds_start": 950,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_148906.3",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asp317Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_683704.2",
"strand": true,
"transcript": "NM_148906.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 719,
"aa_ref": "D",
"aa_start": 317,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2786,
"cdna_start": 969,
"cds_end": null,
"cds_length": 2160,
"cds_start": 950,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000888376.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asp317Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558435.1",
"strand": true,
"transcript": "ENST00000888376.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 714,
"aa_ref": "D",
"aa_start": 321,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2770,
"cdna_start": 981,
"cds_end": null,
"cds_length": 2145,
"cds_start": 962,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000888377.1",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.962A>G",
"hgvs_p": "p.Asp321Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558436.1",
"strand": true,
"transcript": "ENST00000888377.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 626,
"aa_ref": "D",
"aa_start": 224,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3436,
"cdna_start": 796,
"cds_end": null,
"cds_length": 1881,
"cds_start": 671,
"consequences": [
"missense_variant"
],
"exon_count": 20,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_148907.3",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.671A>G",
"hgvs_p": "p.Asp224Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_683705.1",
"strand": true,
"transcript": "NM_148907.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 571,
"aa_ref": "D",
"aa_start": 169,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3598,
"cdna_start": 958,
"cds_end": null,
"cds_length": 1716,
"cds_start": 506,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001330580.2",
"gene_hgnc_id": 16386,
"gene_symbol": "OSBPL9",
"hgvs_c": "c.506A>G",
"hgvs_p": "p.Asp169Gly",
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