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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: 14-23387643-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=23387643&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 21,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS1",
"BS2"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "MYH6",
"hgnc_id": 7576,
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -21,
"transcript": "NM_002471.4",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
"acmg_score": -21,
"allele_count_reference_population": 469,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.64,
"chr": "14",
"clinvar_classification": "Benign/Likely benign",
"clinvar_disease": " susceptibility to,Atrial septal defect 3,Cardiovascular phenotype,Dilated cardiomyopathy 1EE,Hypertrophic cardiomyopathy 1,Hypertrophic cardiomyopathy 14,Sick sinus syndrome 3,not provided,not specified",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:5 B:2",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.6399999856948853,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5940,
"cdna_start": 4603,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "NM_002471.4",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000405093.9",
"protein_coding": true,
"protein_id": "NP_002462.2",
"strand": false,
"transcript": "NM_002471.4",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5940,
"cdna_start": 4603,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000405093.9",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_002471.4",
"protein_coding": true,
"protein_id": "ENSP00000386041.3",
"strand": false,
"transcript": "ENST00000405093.9",
"transcript_support_level": 5
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1950,
"aa_ref": "S",
"aa_start": 1523,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6363,
"cdna_start": 4640,
"cds_end": null,
"cds_length": 5853,
"cds_start": 4569,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968262.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4569G>A",
"hgvs_p": "p.Ser1523Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638321.1",
"strand": false,
"transcript": "ENST00000968262.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1947,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6407,
"cdna_start": 4635,
"cds_end": null,
"cds_length": 5844,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968257.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638316.1",
"strand": false,
"transcript": "ENST00000968257.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1946,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5970,
"cdna_start": 4608,
"cds_end": null,
"cds_length": 5841,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968271.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638330.1",
"strand": false,
"transcript": "ENST00000968271.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1945,
"aa_ref": "S",
"aa_start": 1518,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6380,
"cdna_start": 4656,
"cds_end": null,
"cds_length": 5838,
"cds_start": 4554,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968258.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4554G>A",
"hgvs_p": "p.Ser1518Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638317.1",
"strand": false,
"transcript": "ENST00000968258.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1945,
"aa_ref": "S",
"aa_start": 1518,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6054,
"cdna_start": 4713,
"cds_end": null,
"cds_length": 5838,
"cds_start": 4554,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968274.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4554G>A",
"hgvs_p": "p.Ser1518Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638333.1",
"strand": false,
"transcript": "ENST00000968274.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1945,
"aa_ref": "S",
"aa_start": 1518,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6107,
"cdna_start": 4767,
"cds_end": null,
"cds_length": 5838,
"cds_start": 4554,
"consequences": [
"synonymous_variant"
],
"exon_count": 38,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000968289.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4554G>A",
"hgvs_p": "p.Ser1518Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638348.1",
"strand": false,
"transcript": "ENST00000968289.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6520,
"cdna_start": 4796,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968250.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638309.1",
"strand": false,
"transcript": "ENST00000968250.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6410,
"cdna_start": 4664,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 38,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000968253.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638312.1",
"strand": false,
"transcript": "ENST00000968253.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6410,
"cdna_start": 4688,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968255.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638314.1",
"strand": false,
"transcript": "ENST00000968255.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6050,
"cdna_start": 4717,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968256.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638315.1",
"strand": false,
"transcript": "ENST00000968256.1",
"transcript_support_level": null
},
{
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"aa_length": 1939,
"aa_ref": "S",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6448,
"cdna_start": 4701,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968259.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638318.1",
"strand": false,
"transcript": "ENST00000968259.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6975,
"cdna_start": 5248,
"cds_end": null,
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"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 38,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000968261.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638320.1",
"strand": false,
"transcript": "ENST00000968261.1",
"transcript_support_level": null
},
{
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"aa_length": 1939,
"aa_ref": "S",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5964,
"cdna_start": 4626,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968281.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638340.1",
"strand": false,
"transcript": "ENST00000968281.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 1939,
"aa_ref": "S",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5998,
"cdna_start": 4658,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 38,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000968282.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638341.1",
"strand": false,
"transcript": "ENST00000968282.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
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"aa_length": 1939,
"aa_ref": "S",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5972,
"cdna_start": 4632,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
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],
"exon_count": 39,
"exon_rank": 32,
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"feature": "ENST00000968283.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000638342.1",
"strand": false,
"transcript": "ENST00000968283.1",
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},
{
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"aa_ref": "S",
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"cdna_length": 6002,
"cdna_start": 4668,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 39,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000968287.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638346.1",
"strand": false,
"transcript": "ENST00000968287.1",
"transcript_support_level": null
},
{
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"aa_ref": "S",
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"cdna_start": 4746,
"cds_end": null,
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"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 38,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000968288.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638347.1",
"strand": false,
"transcript": "ENST00000968288.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1939,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6352,
"cdna_start": 5010,
"cds_end": null,
"cds_length": 5820,
"cds_start": 4536,
"consequences": [
"synonymous_variant"
],
"exon_count": 37,
"exon_rank": 30,
"exon_rank_end": null,
"feature": "ENST00000968290.1",
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"hgvs_c": "c.4536G>A",
"hgvs_p": "p.Ser1512Ser",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000638349.1",
"strand": false,
"transcript": "ENST00000968290.1",
"transcript_support_level": null
},
{
"aa_alt": "S",
"aa_end": null,
"aa_length": 1938,
"aa_ref": "S",
"aa_start": 1512,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6440,
"cdna_start": 4697,
"cds_end": null,
"cds_length": 5817,
"cds_start": 4536,
"consequences": [
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"frequency_reference_population": 0.00029057052,
"gene_hgnc_id": 7576,
"gene_symbol": "MYH6",
"gnomad_exomes_ac": 429,
"gnomad_exomes_af": 0.000293457,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_ac": 40,
"gnomad_genomes_af": 0.000262843,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 1,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Benign/Likely benign",
"phenotype_combined": "not specified|Cardiovascular phenotype|Hypertrophic cardiomyopathy 14|not provided|Atrial septal defect 3;Hypertrophic cardiomyopathy 1;Dilated cardiomyopathy 1EE;Hypertrophic cardiomyopathy 14;Sick sinus syndrome 3, susceptibility to",
"phylop100way_prediction": "Benign",
"phylop100way_score": -6.48,
"pos": 23387643,
"ref": "C",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0.05000000074505806,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0.05,
"transcript": "NM_002471.4"
}
]
}