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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: 2-23757655-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=23757655&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 23757655,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001354107.2",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3841C>A",
"hgvs_p": "p.Pro1281Thr",
"transcript": "NM_017552.4",
"protein_id": "NP_060022.2",
"transcript_support_level": null,
"aa_start": 1281,
"aa_end": null,
"aa_length": 1458,
"cds_start": 3841,
"cds_end": null,
"cds_length": 4377,
"cdna_start": 4194,
"cdna_end": null,
"cdna_length": 8112,
"mane_select": "ENST00000238789.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017552.4"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3841C>A",
"hgvs_p": "p.Pro1281Thr",
"transcript": "ENST00000238789.10",
"protein_id": "ENSP00000238789.5",
"transcript_support_level": 5,
"aa_start": 1281,
"aa_end": null,
"aa_length": 1458,
"cds_start": 3841,
"cds_end": null,
"cds_length": 4377,
"cdna_start": 4194,
"cdna_end": null,
"cdna_length": 8112,
"mane_select": "NM_017552.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000238789.10"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.1666C>A",
"hgvs_p": "p.Pro556Thr",
"transcript": "ENST00000381024.4",
"protein_id": "ENSP00000370412.4",
"transcript_support_level": 1,
"aa_start": 556,
"aa_end": null,
"aa_length": 733,
"cds_start": 1666,
"cds_end": null,
"cds_length": 2202,
"cdna_start": 1668,
"cdna_end": null,
"cdna_length": 5579,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000381024.4"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3868C>A",
"hgvs_p": "p.Pro1290Thr",
"transcript": "NM_001354107.2",
"protein_id": "NP_001341036.1",
"transcript_support_level": null,
"aa_start": 1290,
"aa_end": null,
"aa_length": 1467,
"cds_start": 3868,
"cds_end": null,
"cds_length": 4404,
"cdna_start": 4221,
"cdna_end": null,
"cdna_length": 8139,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001354107.2"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3826C>A",
"hgvs_p": "p.Pro1276Thr",
"transcript": "NM_001242338.3",
"protein_id": "NP_001229267.2",
"transcript_support_level": null,
"aa_start": 1276,
"aa_end": null,
"aa_length": 1453,
"cds_start": 3826,
"cds_end": null,
"cds_length": 4362,
"cdna_start": 4179,
"cdna_end": null,
"cdna_length": 8097,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001242338.3"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3826C>A",
"hgvs_p": "p.Pro1276Thr",
"transcript": "ENST00000925212.1",
"protein_id": "ENSP00000595271.1",
"transcript_support_level": null,
"aa_start": 1276,
"aa_end": null,
"aa_length": 1440,
"cds_start": 3826,
"cds_end": null,
"cds_length": 4323,
"cdna_start": 4187,
"cdna_end": null,
"cdna_length": 8066,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925212.1"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3826C>A",
"hgvs_p": "p.Pro1276Thr",
"transcript": "XM_047444799.1",
"protein_id": "XP_047300755.1",
"transcript_support_level": null,
"aa_start": 1276,
"aa_end": null,
"aa_length": 1522,
"cds_start": 3826,
"cds_end": null,
"cds_length": 4569,
"cdna_start": 4179,
"cdna_end": null,
"cdna_length": 18110,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047444799.1"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3883C>A",
"hgvs_p": "p.Pro1295Thr",
"transcript": "XM_011532918.4",
"protein_id": "XP_011531220.1",
"transcript_support_level": null,
"aa_start": 1295,
"aa_end": null,
"aa_length": 1511,
"cds_start": 3883,
"cds_end": null,
"cds_length": 4536,
"cdna_start": 4236,
"cdna_end": null,
"cdna_length": 5631,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011532918.4"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3868C>A",
"hgvs_p": "p.Pro1290Thr",
"transcript": "XM_011532919.4",
"protein_id": "XP_011531221.1",
"transcript_support_level": null,
"aa_start": 1290,
"aa_end": null,
"aa_length": 1506,
"cds_start": 3868,
"cds_end": null,
"cds_length": 4521,
"cdna_start": 4221,
"cdna_end": null,
"cdna_length": 5616,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011532919.4"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3841C>A",
"hgvs_p": "p.Pro1281Thr",
"transcript": "XM_011532920.4",
"protein_id": "XP_011531222.1",
"transcript_support_level": null,
"aa_start": 1281,
"aa_end": null,
"aa_length": 1497,
"cds_start": 3841,
"cds_end": null,
"cds_length": 4494,
"cdna_start": 4194,
"cdna_end": null,
"cdna_length": 5589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011532920.4"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3883C>A",
"hgvs_p": "p.Pro1295Thr",
"transcript": "XM_005264372.5",
"protein_id": "XP_005264429.2",
"transcript_support_level": null,
"aa_start": 1295,
"aa_end": null,
"aa_length": 1472,
"cds_start": 3883,
"cds_end": null,
"cds_length": 4419,
"cdna_start": 4236,
"cdna_end": null,
"cdna_length": 8154,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005264372.5"
},
{
"aa_ref": "P",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3883C>A",
"hgvs_p": "p.Pro1295Thr",
"transcript": "XM_006712030.5",
"protein_id": "XP_006712093.1",
"transcript_support_level": null,
"aa_start": 1295,
"aa_end": null,
"aa_length": 1460,
"cds_start": 3883,
"cds_end": null,
"cds_length": 4383,
"cdna_start": 4236,
"cdna_end": null,
"cdna_length": 17882,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006712030.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3808+33C>A",
"hgvs_p": null,
"transcript": "ENST00000925213.1",
"protein_id": "ENSP00000595272.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1368,
"cds_start": null,
"cds_end": null,
"cds_length": 4107,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7788,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925213.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3793+33C>A",
"hgvs_p": null,
"transcript": "ENST00000925211.1",
"protein_id": "ENSP00000595270.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1363,
"cds_start": null,
"cds_end": null,
"cds_length": 4092,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7858,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925211.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "c.3395-2881C>A",
"hgvs_p": null,
"transcript": "ENST00000925214.1",
"protein_id": "ENSP00000595273.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1230,
"cds_start": null,
"cds_end": null,
"cds_length": 3693,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7367,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925214.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "n.2986C>A",
"hgvs_p": null,
"transcript": "ENST00000474583.5",
"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": 3765,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000474583.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "n.4263C>A",
"hgvs_p": null,
"transcript": "NR_125717.2",
"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": 8181,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_125717.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"hgvs_c": "n.4236C>A",
"hgvs_p": null,
"transcript": "XR_001738780.3",
"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": 17412,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_001738780.3"
}
],
"gene_symbol": "ATAD2B",
"gene_hgnc_id": 29230,
"dbsnp": "rs372338525",
"frequency_reference_population": 0.0000012394047,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 6.84229e-7,
"gnomad_genomes_af": 0.00000657117,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09320136904716492,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.167,
"revel_prediction": "Benign",
"alphamissense_score": 0.0706,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.29,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.335,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.05,
"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_001354107.2",
"gene_symbol": "ATAD2B",
"hgnc_id": 29230,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.3868C>A",
"hgvs_p": "p.Pro1290Thr"
}
],
"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
}