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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: 7-26346450-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=26346450&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "SNX10",
"hgnc_id": 14974,
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"inheritance_mode": "AR",
"pathogenic_score": 2,
"score": 2,
"transcript": "NM_013322.3",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_score": 2,
"allele_count_reference_population": 1,
"alphamissense_prediction": null,
"alphamissense_score": 0.0835,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.17,
"chr": "7",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Uncertain_significance",
"computational_score_selected": 0.5589562654495239,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2665,
"cdna_start": 256,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_013322.3",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000338523.9",
"protein_coding": true,
"protein_id": "NP_037454.2",
"strand": true,
"transcript": "NM_013322.3",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2665,
"cdna_start": 256,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000338523.9",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_013322.3",
"protein_coding": true,
"protein_id": "ENSP00000343709.5",
"strand": true,
"transcript": "ENST00000338523.9",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2491,
"cdna_start": 136,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000396376.5",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000379661.1",
"strand": true,
"transcript": "ENST00000396376.5",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2613,
"cdna_start": 270,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000446848.6",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000395474.3",
"strand": true,
"transcript": "ENST00000446848.6",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 223,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2932,
"cdna_start": 543,
"cds_end": null,
"cds_length": 672,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000698087.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513557.1",
"strand": true,
"transcript": "ENST00000698087.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 223,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2590,
"cdna_start": 173,
"cds_end": null,
"cds_length": 672,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000911861.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000581920.1",
"strand": true,
"transcript": "ENST00000911861.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2625,
"cdna_start": 270,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001199835.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001186764.1",
"strand": true,
"transcript": "NM_001199835.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2568,
"cdna_start": 159,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001318199.3",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001305128.1",
"strand": true,
"transcript": "NM_001318199.3",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2599,
"cdna_start": 267,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000698078.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513550.1",
"strand": true,
"transcript": "ENST00000698078.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2517,
"cdna_start": 185,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000698079.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513551.1",
"strand": true,
"transcript": "ENST00000698079.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2882,
"cdna_start": 550,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000698080.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513552.1",
"strand": true,
"transcript": "ENST00000698080.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2519,
"cdna_start": 187,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000698088.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513558.1",
"strand": true,
"transcript": "ENST00000698088.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2879,
"cdna_start": 547,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000698090.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000513560.1",
"strand": true,
"transcript": "ENST00000698090.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2737,
"cdna_start": 386,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905668.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575727.1",
"strand": true,
"transcript": "ENST00000905668.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2708,
"cdna_start": 357,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000905669.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575728.1",
"strand": true,
"transcript": "ENST00000905669.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2697,
"cdna_start": 346,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000905670.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575729.1",
"strand": true,
"transcript": "ENST00000905670.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2666,
"cdna_start": 315,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000905671.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575730.1",
"strand": true,
"transcript": "ENST00000905671.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
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"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2636,
"cdna_start": 285,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905672.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575731.1",
"strand": true,
"transcript": "ENST00000905672.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2609,
"cdna_start": 266,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905673.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575732.1",
"strand": true,
"transcript": "ENST00000905673.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
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"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2691,
"cdna_start": 340,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000911860.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000581919.1",
"strand": true,
"transcript": "ENST00000911860.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 201,
"aa_ref": "P",
"aa_start": 3,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2632,
"cdna_start": 281,
"cds_end": null,
"cds_length": 606,
"cds_start": 8,
"consequences": [
"missense_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000967692.1",
"gene_hgnc_id": 14974,
"gene_symbol": "SNX10",
"hgvs_c": "c.8C>G",
"hgvs_p": "p.Pro3Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000637751.1",
"strand": true,
"transcript": "ENST00000967692.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
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