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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: 9-137106299-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=137106299&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 20,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "MAN1B1",
"hgnc_id": 6823,
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -20,
"transcript": "NM_016219.5",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_score": -20,
"allele_count_reference_population": 1464,
"alphamissense_prediction": null,
"alphamissense_score": 0.3177,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.19,
"chr": "9",
"clinvar_classification": "Benign/Likely benign",
"clinvar_disease": "Inborn genetic diseases,Rafiq syndrome,not provided",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3 B:2",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.010476380586624146,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 699,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2707,
"cdna_start": 1444,
"cds_end": null,
"cds_length": 2100,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_016219.5",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000371589.9",
"protein_coding": true,
"protein_id": "NP_057303.2",
"strand": true,
"transcript": "NM_016219.5",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 699,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2707,
"cdna_start": 1444,
"cds_end": null,
"cds_length": 2100,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000371589.9",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_016219.5",
"protein_coding": true,
"protein_id": "ENSP00000360645.4",
"strand": true,
"transcript": "ENST00000371589.9",
"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": 2816,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000371587.9",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "n.*1131G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000483132.2",
"strand": true,
"transcript": "ENST00000371587.9",
"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": 2449,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000544448.6",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "n.1429G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000444966.2",
"strand": true,
"transcript": "ENST00000544448.6",
"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": 2816,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000371587.9",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "n.*1131G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000483132.2",
"strand": true,
"transcript": "ENST00000371587.9",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 796,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2698,
"cdna_start": 1572,
"cds_end": null,
"cds_length": 2391,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000682881.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000506762.1",
"strand": true,
"transcript": "ENST00000682881.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 731,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3432,
"cdna_start": 1444,
"cds_end": null,
"cds_length": 2196,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000535144.6",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000441398.3",
"strand": true,
"transcript": "ENST00000535144.6",
"transcript_support_level": 2
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 726,
"aa_ref": "G",
"aa_start": 504,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2801,
"cdna_start": 1541,
"cds_end": null,
"cds_length": 2181,
"cds_start": 1510,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000877685.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1510G>A",
"hgvs_p": "p.Gly504Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000547744.1",
"strand": true,
"transcript": "ENST00000877685.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 725,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2671,
"cdna_start": 1444,
"cds_end": null,
"cds_length": 2178,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000682212.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508217.1",
"strand": true,
"transcript": "ENST00000682212.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 724,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2700,
"cdna_start": 1444,
"cds_end": null,
"cds_length": 2175,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000684759.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000507818.1",
"strand": true,
"transcript": "ENST00000684759.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 722,
"aa_ref": "G",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2777,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 2169,
"cds_start": 1498,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000877687.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1498G>A",
"hgvs_p": "p.Gly500Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000547746.1",
"strand": true,
"transcript": "ENST00000877687.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 717,
"aa_ref": "G",
"aa_start": 495,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2795,
"cdna_start": 1528,
"cds_end": null,
"cds_length": 2154,
"cds_start": 1483,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000916528.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1483G>A",
"hgvs_p": "p.Gly495Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000586587.1",
"strand": true,
"transcript": "ENST00000916528.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 698,
"aa_ref": "G",
"aa_start": 476,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2801,
"cdna_start": 1556,
"cds_end": null,
"cds_length": 2097,
"cds_start": 1426,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000683324.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1426G>A",
"hgvs_p": "p.Gly476Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000507373.1",
"strand": true,
"transcript": "ENST00000683324.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 698,
"aa_ref": "G",
"aa_start": 476,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2806,
"cdna_start": 1539,
"cds_end": null,
"cds_length": 2097,
"cds_start": 1426,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000916526.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1426G>A",
"hgvs_p": "p.Gly476Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000586585.1",
"strand": true,
"transcript": "ENST00000916526.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 698,
"aa_ref": "G",
"aa_start": 476,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2740,
"cdna_start": 1479,
"cds_end": null,
"cds_length": 2097,
"cds_start": 1426,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000916527.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1426G>A",
"hgvs_p": "p.Gly476Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000586586.1",
"strand": true,
"transcript": "ENST00000916527.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 697,
"aa_ref": "G",
"aa_start": 475,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2698,
"cdna_start": 1438,
"cds_end": null,
"cds_length": 2094,
"cds_start": 1423,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000684144.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1423G>A",
"hgvs_p": "p.Gly475Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508213.1",
"strand": true,
"transcript": "ENST00000684144.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 697,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2717,
"cdna_start": 1460,
"cds_end": null,
"cds_length": 2094,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000916531.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000586590.1",
"strand": true,
"transcript": "ENST00000916531.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 686,
"aa_ref": "G",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2690,
"cdna_start": 1464,
"cds_end": null,
"cds_length": 2061,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000682117.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1429G>A",
"hgvs_p": "p.Gly477Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000507328.1",
"strand": true,
"transcript": "ENST00000682117.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 680,
"aa_ref": "G",
"aa_start": 458,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2667,
"cdna_start": 1407,
"cds_end": null,
"cds_length": 2043,
"cds_start": 1372,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000877684.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1372G>A",
"hgvs_p": "p.Gly458Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000547743.1",
"strand": true,
"transcript": "ENST00000877684.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 678,
"aa_ref": "G",
"aa_start": 456,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2664,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 2037,
"cds_start": 1366,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000916530.1",
"gene_hgnc_id": 6823,
"gene_symbol": "MAN1B1",
"hgvs_c": "c.1366G>A",
"hgvs_p": "p.Gly456Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000586589.1",
"strand": true,
"transcript": "ENST00000916530.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 675,
"aa_ref": "G",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2663,
"cdna_start": 1402,
"cds_end": null,
"cds_length": 2028,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 9,
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