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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: 6-157207463-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=157207463&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PVS1",
"PM2",
"PP5_Very_Strong"
],
"effects": [
"stop_gained"
],
"gene_symbol": "ARID1B",
"hgnc_id": 18040,
"hgvs_c": "c.6820C>T",
"hgvs_p": "p.Gln2274*",
"inheritance_mode": "AD",
"pathogenic_score": 18,
"score": 18,
"transcript": "NM_001438482.1",
"verdict": "Pathogenic"
}
],
"acmg_classification": "Pathogenic",
"acmg_criteria": "PVS1,PM2,PP5_Very_Strong",
"acmg_score": 18,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.66,
"chr": "6",
"clinvar_classification": "Pathogenic",
"clinvar_disease": "ARID1B-related BAFopathy,Coffin-Siris syndrome 1,Inborn genetic diseases",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:3",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.6600000262260437,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "*",
"aa_end": null,
"aa_length": 2372,
"aa_ref": "Q",
"aa_start": 2231,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10310,
"cdna_start": 6994,
"cds_end": null,
"cds_length": 7119,
"cds_start": 6691,
"consequences": [
"stop_gained"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001374828.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6691C>T",
"hgvs_p": "p.Gln2231*",
"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": "*",
"aa_end": null,
"aa_length": 2372,
"aa_ref": "Q",
"aa_start": 2231,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 10310,
"cdna_start": 6994,
"cds_end": null,
"cds_length": 7119,
"cds_start": 6691,
"consequences": [
"stop_gained"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "ENST00000636930.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6691C>T",
"hgvs_p": "p.Gln2231*",
"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": "*",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "Q",
"aa_start": 2191,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10813,
"cdna_start": 7497,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6571,
"consequences": [
"stop_gained"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000346085.10",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6571C>T",
"hgvs_p": "p.Gln2191*",
"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": "*",
"aa_end": null,
"aa_length": 2319,
"aa_ref": "Q",
"aa_start": 2178,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8211,
"cdna_start": 6532,
"cds_end": null,
"cds_length": 6960,
"cds_start": 6532,
"consequences": [
"stop_gained"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "ENST00000350026.11",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6532C>T",
"hgvs_p": "p.Gln2178*",
"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": "*",
"aa_end": null,
"aa_length": 1486,
"aa_ref": "Q",
"aa_start": 1345,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5073,
"cdna_start": 4175,
"cds_end": null,
"cds_length": 4461,
"cds_start": 4033,
"consequences": [
"stop_gained"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000637810.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4033C>T",
"hgvs_p": "p.Gln1345*",
"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": "*",
"aa_end": null,
"aa_length": 2415,
"aa_ref": "Q",
"aa_start": 2274,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10439,
"cdna_start": 7123,
"cds_end": null,
"cds_length": 7248,
"cds_start": 6820,
"consequences": [
"stop_gained"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001438482.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6820C>T",
"hgvs_p": "p.Gln2274*",
"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": "*",
"aa_end": null,
"aa_length": 2415,
"aa_ref": "Q",
"aa_start": 2274,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8616,
"cdna_start": 6820,
"cds_end": null,
"cds_length": 7248,
"cds_start": 6820,
"consequences": [
"stop_gained"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "ENST00000637015.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6820C>T",
"hgvs_p": "p.Gln2274*",
"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": "*",
"aa_end": null,
"aa_length": 2386,
"aa_ref": "Q",
"aa_start": 2245,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10352,
"cdna_start": 7036,
"cds_end": null,
"cds_length": 7161,
"cds_start": 6733,
"consequences": [
"stop_gained"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001438483.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6733C>T",
"hgvs_p": "p.Gln2245*",
"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": "*",
"aa_end": null,
"aa_length": 2366,
"aa_ref": "Q",
"aa_start": 2225,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8568,
"cdna_start": 6772,
"cds_end": null,
"cds_length": 7101,
"cds_start": 6673,
"consequences": [
"stop_gained"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "ENST00000938503.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6673C>T",
"hgvs_p": "p.Gln2225*",
"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": "*",
"aa_end": null,
"aa_length": 2342,
"aa_ref": "Q",
"aa_start": 2201,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10220,
"cdna_start": 6904,
"cds_end": null,
"cds_length": 7029,
"cds_start": 6601,
"consequences": [
"stop_gained"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_001438485.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6601C>T",
"hgvs_p": "p.Gln2201*",
"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": "*",
"aa_end": null,
"aa_length": 2342,
"aa_ref": "Q",
"aa_start": 2201,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8280,
"cdna_start": 6601,
"cds_end": null,
"cds_length": 7029,
"cds_start": 6601,
"consequences": [
"stop_gained"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "ENST00000414678.8",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6601C>T",
"hgvs_p": "p.Gln2201*",
"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": "*",
"aa_end": null,
"aa_length": 2333,
"aa_ref": "Q",
"aa_start": 2192,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10193,
"cdna_start": 6877,
"cds_end": null,
"cds_length": 7002,
"cds_start": 6574,
"consequences": [
"stop_gained"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001438486.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6574C>T",
"hgvs_p": "p.Gln2192*",
"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": "*",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "Q",
"aa_start": 2191,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10807,
"cdna_start": 7491,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6571,
"consequences": [
"stop_gained"
],
"exon_count": 21,
"exon_rank": 21,
"exon_rank_end": null,
"feature": "NM_001371656.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6571C>T",
"hgvs_p": "p.Gln2191*",
"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": "*",
"aa_end": null,
"aa_length": 2332,
"aa_ref": "Q",
"aa_start": 2191,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10190,
"cdna_start": 6874,
"cds_end": null,
"cds_length": 6999,
"cds_start": 6571,
"consequences": [
"stop_gained"
],
"exon_count": 20,
"exon_rank": 20,
"exon_rank_end": null,
"feature": "NM_001374820.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6571C>T",
"hgvs_p": "p.Gln2191*",
"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": "*",
"aa_end": null,
"aa_length": 2319,
"aa_ref": "Q",
"aa_start": 2178,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10151,
"cdna_start": 6835,
"cds_end": null,
"cds_length": 6960,
"cds_start": 6532,
"consequences": [
"stop_gained"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_017519.3",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6532C>T",
"hgvs_p": "p.Gln2178*",
"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": "*",
"aa_end": null,
"aa_length": 2312,
"aa_ref": "Q",
"aa_start": 2171,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10130,
"cdna_start": 6814,
"cds_end": null,
"cds_length": 6939,
"cds_start": 6511,
"consequences": [
"stop_gained"
],
"exon_count": 19,
"exon_rank": 19,
"exon_rank_end": null,
"feature": "NM_001438487.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.6511C>T",
"hgvs_p": "p.Gln2171*",
"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": "*",
"aa_end": null,
"aa_length": 1539,
"aa_ref": "Q",
"aa_start": 1398,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7897,
"cdna_start": 4581,
"cds_end": null,
"cds_length": 4620,
"cds_start": 4192,
"consequences": [
"stop_gained"
],
"exon_count": 18,
"exon_rank": 18,
"exon_rank_end": null,
"feature": "NM_001363725.2",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4192C>T",
"hgvs_p": "p.Gln1398*",
"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": "*",
"aa_end": null,
"aa_length": 1539,
"aa_ref": "Q",
"aa_start": 1398,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5913,
"cdna_start": 4693,
"cds_end": null,
"cds_length": 4620,
"cds_start": 4192,
"consequences": [
"stop_gained"
],
"exon_count": 18,
"exon_rank": 18,
"exon_rank_end": null,
"feature": "ENST00000637904.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4192C>T",
"hgvs_p": "p.Gln1398*",
"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": "*",
"aa_end": null,
"aa_length": 1486,
"aa_ref": "Q",
"aa_start": 1345,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7738,
"cdna_start": 4422,
"cds_end": null,
"cds_length": 4461,
"cds_start": 4033,
"consequences": [
"stop_gained"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_001438488.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4033C>T",
"hgvs_p": "p.Gln1345*",
"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": "*",
"aa_end": null,
"aa_length": 1479,
"aa_ref": "Q",
"aa_start": 1338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5830,
"cdna_start": 4599,
"cds_end": null,
"cds_length": 4440,
"cds_start": 4012,
"consequences": [
"stop_gained"
],
"exon_count": 17,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000635849.1",
"gene_hgnc_id": 18040,
"gene_symbol": "ARID1B",
"hgvs_c": "c.4012C>T",
"hgvs_p": "p.Gln1338*",
"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": "*",
"aa_end": null,
"aa_length": 1348,
"aa_ref": "Q",
"aa_start": 1215,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4048,
"cdna_start": 3643,
"cds_end": null,
"cds_length": 4048,
"cds_start": 3643,
"consequences": [
"stop_gained"
],
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