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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: 10-124400941-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=124400941&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PS3",
"PM2",
"PP2",
"PP3_Strong",
"PP5_Very_Strong"
],
"effects": [
"missense_variant"
],
"gene_symbol": "OAT",
"hgnc_id": 8091,
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"inheritance_mode": "AR",
"pathogenic_score": 19,
"score": 19,
"transcript": "NM_000274.4",
"verdict": "Pathogenic"
}
],
"acmg_classification": "Pathogenic",
"acmg_criteria": "PS3,PM2,PP2,PP3_Strong,PP5_Very_Strong",
"acmg_score": 19,
"allele_count_reference_population": 49,
"alphamissense_prediction": null,
"alphamissense_score": 0.9796,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.43,
"chr": "10",
"clinvar_classification": "Pathogenic/Likely pathogenic",
"clinvar_disease": "Ornithine aminotransferase deficiency,not provided",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:1 LP:1",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.9835277795791626,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2039,
"cdna_start": 1138,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_000274.4",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000368845.6",
"protein_coding": true,
"protein_id": "NP_000265.1",
"strand": false,
"transcript": "NM_000274.4",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2039,
"cdna_start": 1138,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000368845.6",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000274.4",
"protein_coding": true,
"protein_id": "ENSP00000357838.5",
"strand": false,
"transcript": "ENST00000368845.6",
"transcript_support_level": 1
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 301,
"aa_ref": "G",
"aa_start": 215,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1864,
"cdna_start": 963,
"cds_end": null,
"cds_length": 906,
"cds_start": 644,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000539214.5",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.644G>A",
"hgvs_p": "p.Gly215Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000439042.1",
"strand": false,
"transcript": "ENST00000539214.5",
"transcript_support_level": 1
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 440,
"aa_ref": "G",
"aa_start": 354,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2056,
"cdna_start": 1150,
"cds_end": null,
"cds_length": 1323,
"cds_start": 1061,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000921313.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1061G>A",
"hgvs_p": "p.Gly354Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000591372.1",
"strand": false,
"transcript": "ENST00000921313.1",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2034,
"cdna_start": 1133,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_001322965.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309894.1",
"strand": false,
"transcript": "NM_001322965.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2354,
"cdna_start": 1453,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001322966.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309895.1",
"strand": false,
"transcript": "NM_001322966.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2159,
"cdna_start": 1258,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001322967.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309896.1",
"strand": false,
"transcript": "NM_001322967.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2246,
"cdna_start": 1345,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001322968.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309897.1",
"strand": false,
"transcript": "NM_001322968.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2126,
"cdna_start": 1225,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001322969.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309898.1",
"strand": false,
"transcript": "NM_001322969.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
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"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2342,
"cdna_start": 1441,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001322970.2",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001309899.1",
"strand": false,
"transcript": "NM_001322970.2",
"transcript_support_level": null
},
{
"aa_alt": "D",
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"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2129,
"cdna_start": 1228,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000858831.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528890.1",
"strand": false,
"transcript": "ENST00000858831.1",
"transcript_support_level": null
},
{
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"aa_ref": "G",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2159,
"cdna_start": 1258,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
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],
"exon_count": 11,
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"feature": "ENST00000858833.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000528892.1",
"strand": false,
"transcript": "ENST00000858833.1",
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},
{
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"cdna_start": 1221,
"cds_end": null,
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"consequences": [
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],
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"feature": "ENST00000858834.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528893.1",
"strand": false,
"transcript": "ENST00000858834.1",
"transcript_support_level": null
},
{
"aa_alt": "D",
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"aa_length": 439,
"aa_ref": "G",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2222,
"cdna_start": 1321,
"cds_end": null,
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"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
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"feature": "ENST00000858835.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528894.1",
"strand": false,
"transcript": "ENST00000858835.1",
"transcript_support_level": null
},
{
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"biotype": "protein_coding",
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"cdna_end": null,
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"cdna_start": 1453,
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"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000858836.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528895.1",
"strand": false,
"transcript": "ENST00000858836.1",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2066,
"cdna_start": 1172,
"cds_end": null,
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"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000858838.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528897.1",
"strand": false,
"transcript": "ENST00000858838.1",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2436,
"cdna_start": 1534,
"cds_end": null,
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"consequences": [
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],
"exon_count": 10,
"exon_rank": 9,
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"feature": "ENST00000858839.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000528898.1",
"strand": false,
"transcript": "ENST00000858839.1",
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},
{
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"biotype": "protein_coding",
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"cds_end": null,
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"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000858840.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000528899.1",
"strand": false,
"transcript": "ENST00000858840.1",
"transcript_support_level": null
},
{
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"aa_ref": "G",
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"biotype": "protein_coding",
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"cdna_end": null,
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"cdna_start": 1180,
"cds_end": null,
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"consequences": [
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],
"exon_count": 10,
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"feature": "ENST00000921311.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000591370.1",
"strand": false,
"transcript": "ENST00000921311.1",
"transcript_support_level": null
},
{
"aa_alt": "D",
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"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2206,
"cdna_start": 1305,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000921312.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
"hgvs_p": "p.Gly353Asp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000591371.1",
"strand": false,
"transcript": "ENST00000921312.1",
"transcript_support_level": null
},
{
"aa_alt": "D",
"aa_end": null,
"aa_length": 439,
"aa_ref": "G",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2034,
"cdna_start": 1133,
"cds_end": null,
"cds_length": 1320,
"cds_start": 1058,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000921315.1",
"gene_hgnc_id": 8091,
"gene_symbol": "OAT",
"hgvs_c": "c.1058G>A",
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