← Back to variant description
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: 14-94463103-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=94463103&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 94463103,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_175739.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "NM_175739.4",
"protein_id": "NP_783866.3",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000674397.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_175739.4"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "ENST00000674397.2",
"protein_id": "ENSP00000501517.1",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_175739.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000674397.2"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1298C>A",
"hgvs_p": "p.Thr433Asn",
"transcript": "ENST00000337425.10",
"protein_id": "ENSP00000337133.5",
"transcript_support_level": 1,
"aa_start": 433,
"aa_end": null,
"aa_length": 435,
"cds_start": 1298,
"cds_end": null,
"cds_length": 1308,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000337425.10"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1004C>A",
"hgvs_p": "p.Thr335Asn",
"transcript": "ENST00000448305.6",
"protein_id": "ENSP00000414092.2",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 337,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000448305.6"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.944C>A",
"hgvs_p": "p.Thr315Asn",
"transcript": "ENST00000298845.12",
"protein_id": "ENSP00000298845.8",
"transcript_support_level": 1,
"aa_start": 315,
"aa_end": null,
"aa_length": 317,
"cds_start": 944,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000298845.12"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.851C>A",
"hgvs_p": "p.Thr284Asn",
"transcript": "ENST00000424550.6",
"protein_id": "ENSP00000409012.2",
"transcript_support_level": 1,
"aa_start": 284,
"aa_end": null,
"aa_length": 286,
"cds_start": 851,
"cds_end": null,
"cds_length": 861,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000424550.6"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1268C>A",
"hgvs_p": "p.Thr423Asn",
"transcript": "ENST00000853990.1",
"protein_id": "ENSP00000524049.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 425,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1278,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853990.1"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "ENST00000380365.7",
"protein_id": "ENSP00000369723.3",
"transcript_support_level": 5,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380365.7"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "ENST00000853989.1",
"protein_id": "ENSP00000524048.1",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853989.1"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1004C>A",
"hgvs_p": "p.Thr335Asn",
"transcript": "NM_001284275.2",
"protein_id": "NP_001271204.2",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 337,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284275.2"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.998C>A",
"hgvs_p": "p.Thr333Asn",
"transcript": "ENST00000674164.1",
"protein_id": "ENSP00000501328.1",
"transcript_support_level": null,
"aa_start": 333,
"aa_end": null,
"aa_length": 335,
"cds_start": 998,
"cds_end": null,
"cds_length": 1008,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000674164.1"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.944C>A",
"hgvs_p": "p.Thr315Asn",
"transcript": "NM_001042518.2",
"protein_id": "NP_001035983.2",
"transcript_support_level": null,
"aa_start": 315,
"aa_end": null,
"aa_length": 317,
"cds_start": 944,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001042518.2"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.851C>A",
"hgvs_p": "p.Thr284Asn",
"transcript": "NM_001284276.2",
"protein_id": "NP_001271205.1",
"transcript_support_level": null,
"aa_start": 284,
"aa_end": null,
"aa_length": 286,
"cds_start": 851,
"cds_end": null,
"cds_length": 861,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284276.2"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "XM_011536714.3",
"protein_id": "XP_011535016.1",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536714.3"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "XM_011536715.3",
"protein_id": "XP_011535017.1",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536715.3"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn",
"transcript": "XM_047431339.1",
"protein_id": "XP_047287295.1",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 417,
"cds_start": 1244,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431339.1"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1004C>A",
"hgvs_p": "p.Thr335Asn",
"transcript": "XM_011536716.3",
"protein_id": "XP_011535018.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 337,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536716.3"
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1004C>A",
"hgvs_p": "p.Thr335Asn",
"transcript": "XM_047431341.1",
"protein_id": "XP_047287297.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 337,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431341.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ENSG00000256357",
"gene_hgnc_id": null,
"hgvs_c": "n.172-1231G>T",
"hgvs_p": null,
"transcript": "ENST00000536735.1",
"protein_id": null,
"transcript_support_level": 4,
"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": "pseudogene",
"feature": "ENST00000536735.1"
}
],
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"dbsnp": "rs371000087",
"frequency_reference_population": 0.0000049584482,
"hom_count_reference_population": 0,
"allele_count_reference_population": 8,
"gnomad_exomes_af": 0.0000047906,
"gnomad_genomes_af": 0.00000656978,
"gnomad_exomes_ac": 7,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.24557700753211975,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.305,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.1335,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.361,
"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": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_175739.4",
"gene_symbol": "SERPINA9",
"hgnc_id": 15995,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1244C>A",
"hgvs_p": "p.Thr415Asn"
},
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000536735.1",
"gene_symbol": "ENSG00000256357",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.172-1231G>T",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}