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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: 3-184276991-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=184276991&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 184276991,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_014693.4",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.226G>C",
"hgvs_p": "p.Gly76Arg",
"transcript": "NM_001100121.2",
"protein_id": "NP_001093591.1",
"transcript_support_level": null,
"aa_start": 76,
"aa_end": null,
"aa_length": 765,
"cds_start": 226,
"cds_end": null,
"cds_length": 2298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000404464.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001100121.2"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.226G>C",
"hgvs_p": "p.Gly76Arg",
"transcript": "ENST00000404464.8",
"protein_id": "ENSP00000385846.3",
"transcript_support_level": 1,
"aa_start": 76,
"aa_end": null,
"aa_length": 765,
"cds_start": 226,
"cds_end": null,
"cds_length": 2298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001100121.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000404464.8"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EEF1AKMT4-ECE2",
"gene_hgnc_id": 53615,
"hgvs_c": "c.580G>C",
"hgvs_p": "p.Gly194Arg",
"transcript": "ENST00000402825.7",
"protein_id": "ENSP00000384223.3",
"transcript_support_level": 1,
"aa_start": 194,
"aa_end": null,
"aa_length": 883,
"cds_start": 580,
"cds_end": null,
"cds_length": 2652,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402825.7"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.364G>C",
"hgvs_p": "p.Gly122Arg",
"transcript": "ENST00000357474.9",
"protein_id": "ENSP00000350066.5",
"transcript_support_level": 1,
"aa_start": 122,
"aa_end": null,
"aa_length": 811,
"cds_start": 364,
"cds_end": null,
"cds_length": 2436,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000357474.9"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.139G>C",
"hgvs_p": "p.Gly47Arg",
"transcript": "ENST00000359140.8",
"protein_id": "ENSP00000352052.4",
"transcript_support_level": 1,
"aa_start": 47,
"aa_end": null,
"aa_length": 736,
"cds_start": 139,
"cds_end": null,
"cds_length": 2211,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000359140.8"
},
{
"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": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "n.62G>C",
"hgvs_p": null,
"transcript": "ENST00000490579.1",
"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": "ENST00000490579.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EEF1AKMT4-ECE2",
"gene_hgnc_id": 53615,
"hgvs_c": "c.580G>C",
"hgvs_p": "p.Gly194Arg",
"transcript": "NM_014693.4",
"protein_id": "NP_055508.3",
"transcript_support_level": null,
"aa_start": 194,
"aa_end": null,
"aa_length": 883,
"cds_start": 580,
"cds_end": null,
"cds_length": 2652,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014693.4"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.364G>C",
"hgvs_p": "p.Gly122Arg",
"transcript": "NM_001100120.2",
"protein_id": "NP_001093590.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 811,
"cds_start": 364,
"cds_end": null,
"cds_length": 2436,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001100120.2"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.364G>C",
"hgvs_p": "p.Gly122Arg",
"transcript": "ENST00000949185.1",
"protein_id": "ENSP00000619244.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 811,
"cds_start": 364,
"cds_end": null,
"cds_length": 2436,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949185.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.364G>C",
"hgvs_p": "p.Gly122Arg",
"transcript": "ENST00000855515.1",
"protein_id": "ENSP00000525574.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 774,
"cds_start": 364,
"cds_end": null,
"cds_length": 2325,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855515.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.139G>C",
"hgvs_p": "p.Gly47Arg",
"transcript": "NM_001037324.3",
"protein_id": "NP_001032401.1",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 736,
"cds_start": 139,
"cds_end": null,
"cds_length": 2211,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001037324.3"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.202G>C",
"hgvs_p": "p.Gly68Arg",
"transcript": "ENST00000430587.1",
"protein_id": "ENSP00000398444.1",
"transcript_support_level": 2,
"aa_start": 68,
"aa_end": null,
"aa_length": 716,
"cds_start": 202,
"cds_end": null,
"cds_length": 2151,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000430587.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.139G>C",
"hgvs_p": "p.Gly47Arg",
"transcript": "ENST00000949186.1",
"protein_id": "ENSP00000619245.1",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 714,
"cds_start": 139,
"cds_end": null,
"cds_length": 2145,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949186.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.139G>C",
"hgvs_p": "p.Gly47Arg",
"transcript": "ENST00000855516.1",
"protein_id": "ENSP00000525575.1",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 709,
"cds_start": 139,
"cds_end": null,
"cds_length": 2130,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855516.1"
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "c.139G>C",
"hgvs_p": "p.Gly47Arg",
"transcript": "ENST00000855514.1",
"protein_id": "ENSP00000525573.1",
"transcript_support_level": null,
"aa_start": 47,
"aa_end": null,
"aa_length": 660,
"cds_start": 139,
"cds_end": null,
"cds_length": 1983,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855514.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "n.139G>C",
"hgvs_p": null,
"transcript": "ENST00000422932.5",
"protein_id": "ENSP00000392467.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000422932.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "n.220G>C",
"hgvs_p": null,
"transcript": "ENST00000474750.1",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000474750.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ECE2",
"gene_hgnc_id": 13275,
"hgvs_c": "n.265G>C",
"hgvs_p": null,
"transcript": "ENST00000488401.5",
"protein_id": null,
"transcript_support_level": 5,
"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": "ENST00000488401.5"
}
],
"gene_symbol": "EEF1AKMT4-ECE2",
"gene_hgnc_id": 53615,
"dbsnp": "rs1246132620",
"frequency_reference_population": 0.0000065703885,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.00000657039,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.7790948748588562,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.592,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.8605,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.07,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 3.471,
"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": 3,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_by_gene": [
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_014693.4",
"gene_symbol": "EEF1AKMT4-ECE2",
"hgnc_id": 53615,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.580G>C",
"hgvs_p": "p.Gly194Arg"
},
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001100120.2",
"gene_symbol": "ECE2",
"hgnc_id": 13275,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.364G>C",
"hgvs_p": "p.Gly122Arg"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}