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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: 6-157207783-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=157207783&ref=A&alt=G&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": "ARID1B",
"hgnc_id": 18040,
"hgvs_c": "c.7140A>G",
"hgvs_p": "p.Glu2380Glu",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -21,
"transcript": "NM_001438482.1",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
"acmg_score": -21,
"allele_count_reference_population": 34,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.62,
"chr": "6",
"clinvar_classification": "Likely benign",
"clinvar_disease": "not provided,not specified",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.6200000047683716,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2372,
"aa_ref": "E",
"aa_start": 2337,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10310,
"cdna_start": 7314,
"cds_end": null,
"cds_length": 7119,
"cds_start": 7011,
"consequences": [
"synonymous_variant"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001374828.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.7011A>G",
"hgvs_p": "p.Glu2337Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000636930.2",
"protein_coding": true,
"protein_id": "NP_001361757.1",
"strand": true,
"transcript": "NM_001374828.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2372,
"aa_ref": "E",
"aa_start": 2337,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 10310,
"cdna_start": 7314,
"cds_end": null,
"cds_length": 7119,
"cds_start": 7011,
"consequences": [
"synonymous_variant"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "ENST00000636930.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.7011A>G",
"hgvs_p": "p.Glu2337Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001374828.1",
"protein_coding": true,
"protein_id": "ENSP00000490491.2",
"strand": true,
"transcript": "ENST00000636930.2",
"transcript_support_level": 2
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "E",
"aa_start": 2297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10813,
"cdna_start": 7817,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6891,
"consequences": [
"synonymous_variant"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000346085.10",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6891A>G",
"hgvs_p": "p.Glu2297Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000344546.5",
"strand": true,
"transcript": "ENST00000346085.10",
"transcript_support_level": 1
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2319,
"aa_ref": "E",
"aa_start": 2284,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8211,
"cdna_start": 6852,
"cds_end": null,
"cds_length": 6960,
"cds_start": 6852,
"consequences": [
"synonymous_variant"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "ENST00000350026.11",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6852A>G",
"hgvs_p": "p.Glu2284Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000055163.8",
"strand": true,
"transcript": "ENST00000350026.11",
"transcript_support_level": 1
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1486,
"aa_ref": "E",
"aa_start": 1451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5073,
"cdna_start": 4495,
"cds_end": null,
"cds_length": 4461,
"cds_start": 4353,
"consequences": [
"synonymous_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000637810.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4353A>G",
"hgvs_p": "p.Glu1451Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000489636.1",
"strand": true,
"transcript": "ENST00000637810.1",
"transcript_support_level": 1
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2415,
"aa_ref": "E",
"aa_start": 2380,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10439,
"cdna_start": 7443,
"cds_end": null,
"cds_length": 7248,
"cds_start": 7140,
"consequences": [
"synonymous_variant"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001438482.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.7140A>G",
"hgvs_p": "p.Glu2380Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425411.1",
"strand": true,
"transcript": "NM_001438482.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2415,
"aa_ref": "E",
"aa_start": 2380,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8616,
"cdna_start": 7140,
"cds_end": null,
"cds_length": 7248,
"cds_start": 7140,
"consequences": [
"synonymous_variant"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000637015.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.7140A>G",
"hgvs_p": "p.Glu2380Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000489729.2",
"strand": true,
"transcript": "ENST00000637015.2",
"transcript_support_level": 5
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2386,
"aa_ref": "E",
"aa_start": 2351,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10352,
"cdna_start": 7356,
"cds_end": null,
"cds_length": 7161,
"cds_start": 7053,
"consequences": [
"synonymous_variant"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001438483.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.7053A>G",
"hgvs_p": "p.Glu2351Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425412.1",
"strand": true,
"transcript": "NM_001438483.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2366,
"aa_ref": "E",
"aa_start": 2331,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8568,
"cdna_start": 7092,
"cds_end": null,
"cds_length": 7101,
"cds_start": 6993,
"consequences": [
"synonymous_variant"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "ENST00000938503.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6993A>G",
"hgvs_p": "p.Glu2331Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000608562.1",
"strand": true,
"transcript": "ENST00000938503.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2342,
"aa_ref": "E",
"aa_start": 2307,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10220,
"cdna_start": 7224,
"cds_end": null,
"cds_length": 7029,
"cds_start": 6921,
"consequences": [
"synonymous_variant"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_001438485.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6921A>G",
"hgvs_p": "p.Glu2307Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425414.1",
"strand": true,
"transcript": "NM_001438485.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2342,
"aa_ref": "E",
"aa_start": 2307,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8280,
"cdna_start": 6921,
"cds_end": null,
"cds_length": 7029,
"cds_start": 6921,
"consequences": [
"synonymous_variant"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "ENST00000414678.8",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6921A>G",
"hgvs_p": "p.Glu2307Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000412835.3",
"strand": true,
"transcript": "ENST00000414678.8",
"transcript_support_level": 5
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2333,
"aa_ref": "E",
"aa_start": 2298,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10193,
"cdna_start": 7197,
"cds_end": null,
"cds_length": 7002,
"cds_start": 6894,
"consequences": [
"synonymous_variant"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001438486.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6894A>G",
"hgvs_p": "p.Glu2298Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425415.1",
"strand": true,
"transcript": "NM_001438486.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "E",
"aa_start": 2297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10807,
"cdna_start": 7811,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6891,
"consequences": [
"synonymous_variant"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001371656.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6891A>G",
"hgvs_p": "p.Glu2297Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001358585.1",
"strand": true,
"transcript": "NM_001371656.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "E",
"aa_start": 2297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10190,
"cdna_start": 7194,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6891,
"consequences": [
"synonymous_variant"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001374820.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6891A>G",
"hgvs_p": "p.Glu2297Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001361749.1",
"strand": true,
"transcript": "NM_001374820.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2319,
"aa_ref": "E",
"aa_start": 2284,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10151,
"cdna_start": 7155,
"cds_end": null,
"cds_length": 6960,
"cds_start": 6852,
"consequences": [
"synonymous_variant"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_017519.3",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6852A>G",
"hgvs_p": "p.Glu2284Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_059989.3",
"strand": true,
"transcript": "NM_017519.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 2312,
"aa_ref": "E",
"aa_start": 2277,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10130,
"cdna_start": 7134,
"cds_end": null,
"cds_length": 6939,
"cds_start": 6831,
"consequences": [
"synonymous_variant"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_001438487.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6831A>G",
"hgvs_p": "p.Glu2277Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425416.1",
"strand": true,
"transcript": "NM_001438487.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1539,
"aa_ref": "E",
"aa_start": 1504,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7897,
"cdna_start": 4901,
"cds_end": null,
"cds_length": 4620,
"cds_start": 4512,
"consequences": [
"synonymous_variant"
],
"exon_count": 18,
"exon_rank": 18,
"exon_rank_end": null,
"feature": "NM_001363725.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4512A>G",
"hgvs_p": "p.Glu1504Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001350654.1",
"strand": true,
"transcript": "NM_001363725.2",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1539,
"aa_ref": "E",
"aa_start": 1504,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5913,
"cdna_start": 5013,
"cds_end": null,
"cds_length": 4620,
"cds_start": 4512,
"consequences": [
"synonymous_variant"
],
"exon_count": 18,
"exon_rank": 18,
"exon_rank_end": null,
"feature": "ENST00000637904.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4512A>G",
"hgvs_p": "p.Glu1504Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000490550.1",
"strand": true,
"transcript": "ENST00000637904.1",
"transcript_support_level": 5
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1486,
"aa_ref": "E",
"aa_start": 1451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7738,
"cdna_start": 4742,
"cds_end": null,
"cds_length": 4461,
"cds_start": 4353,
"consequences": [
"synonymous_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_001438488.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4353A>G",
"hgvs_p": "p.Glu1451Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425417.1",
"strand": true,
"transcript": "NM_001438488.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1479,
"aa_ref": "E",
"aa_start": 1444,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5830,
"cdna_start": 4919,
"cds_end": null,
"cds_length": 4440,
"cds_start": 4332,
"consequences": [
"synonymous_variant"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000635849.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4332A>G",
"hgvs_p": "p.Glu1444Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000490948.1",
"strand": true,
"transcript": "ENST00000635849.1",
"transcript_support_level": 5
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 1348,
"aa_ref": "E",
"aa_start": 1321,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4048,
"cdna_start": 3963,
"cds_end": null,
"cds_length": 4048,
"cds_start": 3963,
"consequences": [
"synonymous_variant"
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