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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: 19-2997941-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=2997941&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 2997941,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001144761.2",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2104C>G",
"hgvs_p": "p.Leu702Val",
"transcript": "ENST00000591529.5",
"protein_id": "ENSP00000468279.1",
"transcript_support_level": 1,
"aa_start": 702,
"aa_end": null,
"aa_length": 706,
"cds_start": 2104,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 2188,
"cdna_end": null,
"cdna_length": 2483,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000591529.5"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2139C>G",
"hgvs_p": "p.Ser713Ser",
"transcript": "NM_003260.5",
"protein_id": "NP_003251.2",
"transcript_support_level": null,
"aa_start": 713,
"aa_end": null,
"aa_length": 743,
"cds_start": 2139,
"cds_end": null,
"cds_length": 2232,
"cdna_start": 2515,
"cdna_end": null,
"cdna_length": 2812,
"mane_select": "ENST00000262953.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003260.5"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2139C>G",
"hgvs_p": "p.Ser713Ser",
"transcript": "ENST00000262953.11",
"protein_id": "ENSP00000262953.5",
"transcript_support_level": 1,
"aa_start": 713,
"aa_end": null,
"aa_length": 743,
"cds_start": 2139,
"cds_end": null,
"cds_length": 2232,
"cdna_start": 2515,
"cdna_end": null,
"cdna_length": 2812,
"mane_select": "NM_003260.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000262953.11"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2142C>G",
"hgvs_p": "p.Ser714Ser",
"transcript": "ENST00000590536.5",
"protein_id": "ENSP00000466542.1",
"transcript_support_level": 1,
"aa_start": 714,
"aa_end": null,
"aa_length": 744,
"cds_start": 2142,
"cds_end": null,
"cds_length": 2235,
"cdna_start": 2251,
"cdna_end": null,
"cdna_length": 2344,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000590536.5"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2104C>G",
"hgvs_p": "p.Leu702Val",
"transcript": "NM_001144761.2",
"protein_id": "NP_001138233.1",
"transcript_support_level": null,
"aa_start": 702,
"aa_end": null,
"aa_length": 706,
"cds_start": 2104,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 2188,
"cdna_end": null,
"cdna_length": 2485,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001144761.2"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2104C>G",
"hgvs_p": "p.Leu702Val",
"transcript": "ENST00000426948.6",
"protein_id": "ENSP00000392869.2",
"transcript_support_level": 5,
"aa_start": 702,
"aa_end": null,
"aa_length": 706,
"cds_start": 2104,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 2104,
"cdna_end": null,
"cdna_length": 2406,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000426948.6"
},
{
"aa_ref": "L",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2065C>G",
"hgvs_p": "p.Leu689Val",
"transcript": "XM_006722864.3",
"protein_id": "XP_006722927.1",
"transcript_support_level": null,
"aa_start": 689,
"aa_end": null,
"aa_length": 693,
"cds_start": 2065,
"cds_end": null,
"cds_length": 2082,
"cdna_start": 2441,
"cdna_end": null,
"cdna_length": 2738,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006722864.3"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2151C>G",
"hgvs_p": "p.Ser717Ser",
"transcript": "ENST00000958739.1",
"protein_id": "ENSP00000628798.1",
"transcript_support_level": null,
"aa_start": 717,
"aa_end": null,
"aa_length": 747,
"cds_start": 2151,
"cds_end": null,
"cds_length": 2244,
"cdna_start": 2504,
"cdna_end": null,
"cdna_length": 2800,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958739.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2142C>G",
"hgvs_p": "p.Ser714Ser",
"transcript": "NM_001300846.2",
"protein_id": "NP_001287775.1",
"transcript_support_level": null,
"aa_start": 714,
"aa_end": null,
"aa_length": 744,
"cds_start": 2142,
"cds_end": null,
"cds_length": 2235,
"cdna_start": 2518,
"cdna_end": null,
"cdna_length": 2815,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300846.2"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2139C>G",
"hgvs_p": "p.Ser713Ser",
"transcript": "ENST00000958737.1",
"protein_id": "ENSP00000628796.1",
"transcript_support_level": null,
"aa_start": 713,
"aa_end": null,
"aa_length": 743,
"cds_start": 2139,
"cds_end": null,
"cds_length": 2232,
"cdna_start": 2243,
"cdna_end": null,
"cdna_length": 2537,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958737.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2133C>G",
"hgvs_p": "p.Ser711Ser",
"transcript": "ENST00000958740.1",
"protein_id": "ENSP00000628799.1",
"transcript_support_level": null,
"aa_start": 711,
"aa_end": null,
"aa_length": 741,
"cds_start": 2133,
"cds_end": null,
"cds_length": 2226,
"cdna_start": 2486,
"cdna_end": null,
"cdna_length": 2778,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958740.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2052C>G",
"hgvs_p": "p.Ser684Ser",
"transcript": "ENST00000958738.1",
"protein_id": "ENSP00000628797.1",
"transcript_support_level": null,
"aa_start": 684,
"aa_end": null,
"aa_length": 714,
"cds_start": 2052,
"cds_end": null,
"cds_length": 2145,
"cdna_start": 2424,
"cdna_end": null,
"cdna_length": 2718,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958738.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.1800C>G",
"hgvs_p": "p.Ser600Ser",
"transcript": "ENST00000881232.1",
"protein_id": "ENSP00000551291.1",
"transcript_support_level": null,
"aa_start": 600,
"aa_end": null,
"aa_length": 630,
"cds_start": 1800,
"cds_end": null,
"cds_length": 1893,
"cdna_start": 2099,
"cdna_end": null,
"cdna_length": 2394,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881232.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.1773C>G",
"hgvs_p": "p.Ser591Ser",
"transcript": "NM_001144762.2",
"protein_id": "NP_001138234.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 621,
"cds_start": 1773,
"cds_end": null,
"cds_length": 1866,
"cdna_start": 1987,
"cdna_end": null,
"cdna_length": 2284,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001144762.2"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.1773C>G",
"hgvs_p": "p.Ser591Ser",
"transcript": "ENST00000443826.7",
"protein_id": "ENSP00000392427.2",
"transcript_support_level": 2,
"aa_start": 591,
"aa_end": null,
"aa_length": 621,
"cds_start": 1773,
"cds_end": null,
"cds_length": 1866,
"cdna_start": 1979,
"cdna_end": null,
"cdna_length": 2238,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000443826.7"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.2106C>G",
"hgvs_p": "p.Ser702Ser",
"transcript": "XM_011528230.2",
"protein_id": "XP_011526532.1",
"transcript_support_level": null,
"aa_start": 702,
"aa_end": null,
"aa_length": 732,
"cds_start": 2106,
"cds_end": null,
"cds_length": 2199,
"cdna_start": 2482,
"cdna_end": null,
"cdna_length": 2779,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528230.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"hgvs_c": "c.257-179C>G",
"hgvs_p": null,
"transcript": "ENST00000586422.5",
"protein_id": "ENSP00000465519.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 119,
"cds_start": null,
"cds_end": null,
"cds_length": 360,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 389,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000586422.5"
}
],
"gene_symbol": "TLE2",
"gene_hgnc_id": 11838,
"dbsnp": "rs373620175",
"frequency_reference_population": 0.000016747801,
"hom_count_reference_population": 1,
"allele_count_reference_population": 27,
"gnomad_exomes_af": 0.0000130135,
"gnomad_genomes_af": 0.0000525866,
"gnomad_exomes_ac": 19,
"gnomad_genomes_ac": 8,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0844067931175232,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.024,
"revel_prediction": "Benign",
"alphamissense_score": 0.19,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.46,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.351,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_001144761.2",
"gene_symbol": "TLE2",
"hgnc_id": 11838,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.2104C>G",
"hgvs_p": "p.Leu702Val"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}