← 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: 5-14487964-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=14487964&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 14487964,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_007118.4",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe",
"transcript": "NM_007118.4",
"protein_id": "NP_009049.2",
"transcript_support_level": null,
"aa_start": 2446,
"aa_end": null,
"aa_length": 3097,
"cds_start": 7336,
"cds_end": null,
"cds_length": 9294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000344204.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_007118.4"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe",
"transcript": "ENST00000344204.9",
"protein_id": "ENSP00000339299.4",
"transcript_support_level": 1,
"aa_start": 2446,
"aa_end": null,
"aa_length": 3097,
"cds_start": 7336,
"cds_end": null,
"cds_length": 9294,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_007118.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000344204.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "n.6254C>T",
"hgvs_p": null,
"transcript": "ENST00000515144.5",
"protein_id": null,
"transcript_support_level": 1,
"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": "ENST00000515144.5"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 51,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.6535C>T",
"hgvs_p": "p.Leu2179Phe",
"transcript": "ENST00000513206.5",
"protein_id": "ENSP00000426342.2",
"transcript_support_level": 5,
"aa_start": 2179,
"aa_end": null,
"aa_length": 2546,
"cds_start": 6535,
"cds_end": null,
"cds_length": 7641,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000513206.5"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe",
"transcript": "XM_017009801.2",
"protein_id": "XP_016865290.1",
"transcript_support_level": null,
"aa_start": 2446,
"aa_end": null,
"aa_length": 3093,
"cds_start": 7336,
"cds_end": null,
"cds_length": 9282,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017009801.2"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7273C>T",
"hgvs_p": "p.Leu2425Phe",
"transcript": "XM_011514107.3",
"protein_id": "XP_011512409.1",
"transcript_support_level": null,
"aa_start": 2425,
"aa_end": null,
"aa_length": 3076,
"cds_start": 7273,
"cds_end": null,
"cds_length": 9231,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514107.3"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 49,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7273C>T",
"hgvs_p": "p.Leu2425Phe",
"transcript": "XM_047417679.1",
"protein_id": "XP_047273635.1",
"transcript_support_level": null,
"aa_start": 2425,
"aa_end": null,
"aa_length": 3076,
"cds_start": 7273,
"cds_end": null,
"cds_length": 9231,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417679.1"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7219C>T",
"hgvs_p": "p.Leu2407Phe",
"transcript": "XM_011514108.2",
"protein_id": "XP_011512410.1",
"transcript_support_level": null,
"aa_start": 2407,
"aa_end": null,
"aa_length": 3058,
"cds_start": 7219,
"cds_end": null,
"cds_length": 9177,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514108.2"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7189C>T",
"hgvs_p": "p.Leu2397Phe",
"transcript": "XM_011514109.4",
"protein_id": "XP_011512411.1",
"transcript_support_level": null,
"aa_start": 2397,
"aa_end": null,
"aa_length": 3048,
"cds_start": 7189,
"cds_end": null,
"cds_length": 9147,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514109.4"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7159C>T",
"hgvs_p": "p.Leu2387Phe",
"transcript": "XM_011514110.4",
"protein_id": "XP_011512412.1",
"transcript_support_level": null,
"aa_start": 2387,
"aa_end": null,
"aa_length": 3038,
"cds_start": 7159,
"cds_end": null,
"cds_length": 9117,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514110.4"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe",
"transcript": "XM_017009802.2",
"protein_id": "XP_016865291.1",
"transcript_support_level": null,
"aa_start": 2446,
"aa_end": null,
"aa_length": 2880,
"cds_start": 7336,
"cds_end": null,
"cds_length": 8643,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017009802.2"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe",
"transcript": "XM_047417681.1",
"protein_id": "XP_047273637.1",
"transcript_support_level": null,
"aa_start": 2446,
"aa_end": null,
"aa_length": 2876,
"cds_start": 7336,
"cds_end": null,
"cds_length": 8631,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417681.1"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 50,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "c.5881C>T",
"hgvs_p": "p.Leu1961Phe",
"transcript": "XM_017009803.2",
"protein_id": "XP_016865292.1",
"transcript_support_level": null,
"aa_start": 1961,
"aa_end": null,
"aa_length": 2612,
"cds_start": 5881,
"cds_end": null,
"cds_length": 7839,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017009803.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "n.2245C>T",
"hgvs_p": null,
"transcript": "ENST00000698542.1",
"protein_id": "ENSP00000513787.1",
"transcript_support_level": null,
"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": "ENST00000698542.1"
},
{
"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": 57,
"intron_rank": 48,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "n.6925+234C>T",
"hgvs_p": null,
"transcript": "ENST00000512070.6",
"protein_id": "ENSP00000421555.2",
"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": "nonsense_mediated_decay",
"feature": "ENST00000512070.6"
},
{
"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": 57,
"intron_rank": 48,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "n.7486+234C>T",
"hgvs_p": null,
"transcript": "NR_134469.2",
"protein_id": null,
"transcript_support_level": null,
"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": "NR_134469.2"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"hgvs_c": "n.*175C>T",
"hgvs_p": null,
"transcript": "ENST00000510281.1",
"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": "ENST00000510281.1"
}
],
"gene_symbol": "TRIO",
"gene_hgnc_id": 12303,
"dbsnp": "rs759324474",
"frequency_reference_population": 0.000022557273,
"hom_count_reference_population": 0,
"allele_count_reference_population": 35,
"gnomad_exomes_af": 0.0000228656,
"gnomad_genomes_af": 0.0000197205,
"gnomad_exomes_ac": 32,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.16338446736335754,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.256,
"revel_prediction": "Benign",
"alphamissense_score": 0.0958,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.13,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.018,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate,BS2",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_007118.4",
"gene_symbol": "TRIO",
"hgnc_id": 12303,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.7336C>T",
"hgvs_p": "p.Leu2446Phe"
}
],
"clinvar_disease": "Inborn genetic diseases",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Inborn genetic diseases",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}