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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: 7-92522121-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=92522121&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 92522121,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_000466.3",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "NM_000466.3",
"protein_id": "NP_000457.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1283,
"cds_start": 254,
"cds_end": null,
"cds_length": 3852,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000248633.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000466.3"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000248633.9",
"protein_id": "ENSP00000248633.4",
"transcript_support_level": 1,
"aa_start": 85,
"aa_end": null,
"aa_length": 1283,
"cds_start": 254,
"cds_end": null,
"cds_length": 3852,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000466.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000248633.9"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000428214.5",
"protein_id": "ENSP00000394413.1",
"transcript_support_level": 1,
"aa_start": 85,
"aa_end": null,
"aa_length": 1226,
"cds_start": 254,
"cds_end": null,
"cds_length": 3681,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000428214.5"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000951788.1",
"protein_id": "ENSP00000621847.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1301,
"cds_start": 254,
"cds_end": null,
"cds_length": 3906,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951788.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000914336.1",
"protein_id": "ENSP00000584395.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1282,
"cds_start": 254,
"cds_end": null,
"cds_length": 3849,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914336.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000914337.1",
"protein_id": "ENSP00000584396.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1281,
"cds_start": 254,
"cds_end": null,
"cds_length": 3846,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914337.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000951786.1",
"protein_id": "ENSP00000621845.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1280,
"cds_start": 254,
"cds_end": null,
"cds_length": 3843,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951786.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000951787.1",
"protein_id": "ENSP00000621846.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1268,
"cds_start": 254,
"cds_end": null,
"cds_length": 3807,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951787.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000951789.1",
"protein_id": "ENSP00000621848.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1256,
"cds_start": 254,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951789.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000951790.1",
"protein_id": "ENSP00000621849.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1255,
"cds_start": 254,
"cds_end": null,
"cds_length": 3768,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000951790.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000901045.1",
"protein_id": "ENSP00000571104.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1243,
"cds_start": 254,
"cds_end": null,
"cds_length": 3732,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901045.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "NM_001282677.2",
"protein_id": "NP_001269606.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1226,
"cds_start": 254,
"cds_end": null,
"cds_length": 3681,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001282677.2"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000914335.1",
"protein_id": "ENSP00000584394.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1217,
"cds_start": 254,
"cds_end": null,
"cds_length": 3654,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914335.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000914338.1",
"protein_id": "ENSP00000584397.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1189,
"cds_start": 254,
"cds_end": null,
"cds_length": 3570,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914338.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "ENST00000438045.5",
"protein_id": "ENSP00000410438.1",
"transcript_support_level": 2,
"aa_start": 85,
"aa_end": null,
"aa_length": 961,
"cds_start": 254,
"cds_end": null,
"cds_length": 2886,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000438045.5"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu",
"transcript": "XM_047420472.1",
"protein_id": "XP_047276428.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 1227,
"cds_start": 254,
"cds_end": null,
"cds_length": 3684,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420472.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.-406G>A",
"hgvs_p": null,
"transcript": "NM_001282678.2",
"protein_id": "NP_001269607.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1075,
"cds_start": null,
"cds_end": null,
"cds_length": 3228,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001282678.2"
},
{
"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": 23,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "c.130-3043G>A",
"hgvs_p": null,
"transcript": "ENST00000914334.1",
"protein_id": "ENSP00000584393.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1235,
"cds_start": null,
"cds_end": null,
"cds_length": 3708,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914334.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"hgvs_c": "n.258G>A",
"hgvs_p": null,
"transcript": "ENST00000484913.5",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000484913.5"
}
],
"gene_symbol": "PEX1",
"gene_hgnc_id": 8850,
"dbsnp": "rs771224088",
"frequency_reference_population": 0.0000099135905,
"hom_count_reference_population": 0,
"allele_count_reference_population": 16,
"gnomad_exomes_af": 0.0000102615,
"gnomad_genomes_af": 0.00000657177,
"gnomad_exomes_ac": 15,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8842498660087585,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.74,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.3907,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.32,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 6.165,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.02,
"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": "Uncertain_significance",
"acmg_criteria": "PP3_Moderate",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_000466.3",
"gene_symbol": "PEX1",
"hgnc_id": 8850,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.254G>A",
"hgvs_p": "p.Gly85Glu"
}
],
"clinvar_disease": "Heimler syndrome 1,Peroxisome biogenesis disorder 1A (Zellweger),Peroxisome biogenesis disorder 1B,Zellweger spectrum disorders,not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:4",
"phenotype_combined": "not provided|Heimler syndrome 1|Heimler syndrome 1;Peroxisome biogenesis disorder 1A (Zellweger);Peroxisome biogenesis disorder 1B|Zellweger spectrum disorders",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}