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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: 16-69366844-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=69366844&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 69366844,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_005652.5",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu",
"transcript": "NM_005652.5",
"protein_id": "NP_005643.2",
"transcript_support_level": null,
"aa_start": 435,
"aa_end": null,
"aa_length": 542,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000254942.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005652.5"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu",
"transcript": "ENST00000254942.8",
"protein_id": "ENSP00000254942.3",
"transcript_support_level": 1,
"aa_start": 435,
"aa_end": null,
"aa_length": 542,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_005652.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000254942.8"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu",
"transcript": "ENST00000903039.1",
"protein_id": "ENSP00000573098.1",
"transcript_support_level": null,
"aa_start": 435,
"aa_end": null,
"aa_length": 541,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903039.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1300G>C",
"hgvs_p": "p.Val434Leu",
"transcript": "ENST00000966429.1",
"protein_id": "ENSP00000636488.1",
"transcript_support_level": null,
"aa_start": 434,
"aa_end": null,
"aa_length": 541,
"cds_start": 1300,
"cds_end": null,
"cds_length": 1626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966429.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu",
"transcript": "ENST00000930142.1",
"protein_id": "ENSP00000600201.1",
"transcript_support_level": null,
"aa_start": 435,
"aa_end": null,
"aa_length": 540,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1623,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930142.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.622G>C",
"hgvs_p": "p.Val208Leu",
"transcript": "ENST00000569584.6",
"protein_id": "ENSP00000475507.1",
"transcript_support_level": 2,
"aa_start": 208,
"aa_end": null,
"aa_length": 243,
"cds_start": 622,
"cds_end": null,
"cds_length": 732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000569584.6"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1312G>C",
"hgvs_p": "p.Val438Leu",
"transcript": "XM_005256121.4",
"protein_id": "XP_005256178.1",
"transcript_support_level": null,
"aa_start": 438,
"aa_end": null,
"aa_length": 545,
"cds_start": 1312,
"cds_end": null,
"cds_length": 1638,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005256121.4"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1312G>C",
"hgvs_p": "p.Val438Leu",
"transcript": "XM_005256122.4",
"protein_id": "XP_005256179.1",
"transcript_support_level": null,
"aa_start": 438,
"aa_end": null,
"aa_length": 544,
"cds_start": 1312,
"cds_end": null,
"cds_length": 1635,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005256122.4"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu",
"transcript": "XM_005256123.4",
"protein_id": "XP_005256180.1",
"transcript_support_level": null,
"aa_start": 435,
"aa_end": null,
"aa_length": 541,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1626,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005256123.4"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1312G>C",
"hgvs_p": "p.Val438Leu",
"transcript": "XM_047434552.1",
"protein_id": "XP_047290508.1",
"transcript_support_level": null,
"aa_start": 438,
"aa_end": null,
"aa_length": 483,
"cds_start": 1312,
"cds_end": null,
"cds_length": 1452,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047434552.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.1069G>C",
"hgvs_p": "p.Val357Leu",
"transcript": "XM_005256124.5",
"protein_id": "XP_005256181.1",
"transcript_support_level": null,
"aa_start": 357,
"aa_end": null,
"aa_length": 464,
"cds_start": 1069,
"cds_end": null,
"cds_length": 1395,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005256124.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "n.141G>C",
"hgvs_p": null,
"transcript": "ENST00000567130.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000567130.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.*91G>C",
"hgvs_p": null,
"transcript": "ENST00000566750.5",
"protein_id": "ENSP00000456022.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 282,
"cds_start": null,
"cds_end": null,
"cds_length": 849,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000566750.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.*205G>C",
"hgvs_p": null,
"transcript": "ENST00000566257.5",
"protein_id": "ENSP00000457094.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 205,
"cds_start": null,
"cds_end": null,
"cds_length": 618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000566257.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "c.*103G>C",
"hgvs_p": null,
"transcript": "ENST00000569542.6",
"protein_id": "ENSP00000462726.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 142,
"cds_start": null,
"cds_end": null,
"cds_length": 429,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000569542.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"hgvs_c": "n.*510G>C",
"hgvs_p": null,
"transcript": "ENST00000564982.6",
"protein_id": "ENSP00000462523.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000564982.6"
}
],
"gene_symbol": "TERF2",
"gene_hgnc_id": 11729,
"dbsnp": "rs372828670",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.06394460797309875,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05999999865889549,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.021,
"revel_prediction": "Benign",
"alphamissense_score": 0.0822,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.54,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.433,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.06,
"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_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_005652.5",
"gene_symbol": "TERF2",
"hgnc_id": 11729,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1303G>C",
"hgvs_p": "p.Val435Leu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}