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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: 9-133031032-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=133031032&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 133031032,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001122823.2",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "NM_012087.4",
"protein_id": "NP_036219.2",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 519,
"cds_start": 21,
"cds_end": null,
"cds_length": 1560,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 2098,
"mane_select": "ENST00000372097.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012087.4"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000372097.10",
"protein_id": "ENSP00000361169.5",
"transcript_support_level": 1,
"aa_start": 7,
"aa_end": null,
"aa_length": 519,
"cds_start": 21,
"cds_end": null,
"cds_length": 1560,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 2098,
"mane_select": "NM_012087.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000372097.10"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000372108.9",
"protein_id": "ENSP00000361180.5",
"transcript_support_level": 1,
"aa_start": 7,
"aa_end": null,
"aa_length": 526,
"cds_start": 21,
"cds_end": null,
"cds_length": 1581,
"cdna_start": 29,
"cdna_end": null,
"cdna_length": 2110,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000372108.9"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "NM_001122823.2",
"protein_id": "NP_001116295.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 526,
"cds_start": 21,
"cds_end": null,
"cds_length": 1581,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 2119,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001122823.2"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000916424.1",
"protein_id": "ENSP00000586483.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 507,
"cds_start": 21,
"cds_end": null,
"cds_length": 1524,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 2062,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916424.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000902265.1",
"protein_id": "ENSP00000572324.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 500,
"cds_start": 21,
"cds_end": null,
"cds_length": 1503,
"cdna_start": 291,
"cdna_end": null,
"cdna_length": 2296,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902265.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000902266.1",
"protein_id": "ENSP00000572325.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 484,
"cds_start": 21,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 60,
"cdna_end": null,
"cdna_length": 2017,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902266.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000916423.1",
"protein_id": "ENSP00000586482.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 467,
"cds_start": 21,
"cds_end": null,
"cds_length": 1404,
"cdna_start": 301,
"cdna_end": null,
"cdna_length": 2204,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916423.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000342018.12",
"protein_id": "ENSP00000339530.7",
"transcript_support_level": 5,
"aa_start": 7,
"aa_end": null,
"aa_length": 457,
"cds_start": 21,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 29,
"cdna_end": null,
"cdna_length": 1905,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000342018.12"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000916426.1",
"protein_id": "ENSP00000586485.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 444,
"cds_start": 21,
"cds_end": null,
"cds_length": 1335,
"cdna_start": 33,
"cdna_end": null,
"cdna_length": 1865,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916426.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "ENST00000916425.1",
"protein_id": "ENSP00000586484.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 279,
"cds_start": 21,
"cds_end": null,
"cds_length": 840,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 1378,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916425.1"
},
{
"aa_ref": "D",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu",
"transcript": "XM_047424080.1",
"protein_id": "XP_047280036.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 537,
"cds_start": 21,
"cds_end": null,
"cds_length": 1614,
"cdna_start": 36,
"cdna_end": null,
"cdna_length": 2244,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047424080.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.-83T>G",
"hgvs_p": null,
"transcript": "NM_001286709.2",
"protein_id": "NP_001273638.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 345,
"cds_start": null,
"cds_end": null,
"cds_length": 1038,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1679,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001286709.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.-83T>G",
"hgvs_p": null,
"transcript": "ENST00000372099.10",
"protein_id": "ENSP00000361171.7",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 345,
"cds_start": null,
"cds_end": null,
"cds_length": 1038,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1999,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000372099.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.-135T>G",
"hgvs_p": null,
"transcript": "ENST00000439697.1",
"protein_id": "ENSP00000393207.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 223,
"cds_start": null,
"cds_end": null,
"cds_length": 673,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 823,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000439697.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.12+122T>G",
"hgvs_p": null,
"transcript": "ENST00000440319.5",
"protein_id": "ENSP00000389498.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 243,
"cds_start": null,
"cds_end": null,
"cds_length": 732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 920,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000440319.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.12+122T>G",
"hgvs_p": null,
"transcript": "XM_047424081.1",
"protein_id": "XP_047280037.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 490,
"cds_start": null,
"cds_end": null,
"cds_length": 1473,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2279,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047424081.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.12+122T>G",
"hgvs_p": null,
"transcript": "XM_017015315.2",
"protein_id": "XP_016870804.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 479,
"cds_start": null,
"cds_end": null,
"cds_length": 1440,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2154,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017015315.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "c.12+122T>G",
"hgvs_p": null,
"transcript": "XM_017015316.2",
"protein_id": "XP_016870805.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 472,
"cds_start": null,
"cds_end": null,
"cds_length": 1419,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2133,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017015316.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "GTF3C5",
"gene_hgnc_id": 4668,
"hgvs_c": "n.15T>G",
"hgvs_p": null,
"transcript": "ENST00000485692.1",
"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": 827,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000485692.1"
}
],
"gene_symbol": "GTF3C5",
"gene_hgnc_id": 4668,
"dbsnp": null,
"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": 0.0693064033985138,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.031,
"revel_prediction": "Benign",
"alphamissense_score": 0.0969,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.72,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.575,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001122823.2",
"gene_symbol": "GTF3C5",
"hgnc_id": 4668,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.21T>G",
"hgvs_p": "p.Asp7Glu"
}
],
"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
}