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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: 16-15888581-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=15888581&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 15888581,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_144600.4",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_144600.4",
"protein_id": "NP_653201.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 174,
"cds_start": 5,
"cds_end": null,
"cds_length": 525,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2264,
"mane_select": "ENST00000255759.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000255759.11",
"protein_id": "ENSP00000255759.6",
"transcript_support_level": 1,
"aa_start": 2,
"aa_end": null,
"aa_length": 174,
"cds_start": 5,
"cds_end": null,
"cds_length": 525,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2264,
"mane_select": "NM_144600.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_001304499.2",
"protein_id": "NP_001291428.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 198,
"cds_start": 5,
"cds_end": null,
"cds_length": 597,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2336,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000573429.5",
"protein_id": "ENSP00000461830.1",
"transcript_support_level": 3,
"aa_start": 2,
"aa_end": null,
"aa_length": 198,
"cds_start": 5,
"cds_end": null,
"cds_length": 597,
"cdna_start": 34,
"cdna_end": null,
"cdna_length": 646,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_001304502.2",
"protein_id": "NP_001291431.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 128,
"cds_start": 5,
"cds_end": null,
"cds_length": 387,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2199,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000573396.5",
"protein_id": "ENSP00000461548.1",
"transcript_support_level": 3,
"aa_start": 2,
"aa_end": null,
"aa_length": 128,
"cds_start": 5,
"cds_end": null,
"cds_length": 387,
"cdna_start": 19,
"cdna_end": null,
"cdna_length": 735,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000575938.1",
"protein_id": "ENSP00000458348.1",
"transcript_support_level": 3,
"aa_start": 2,
"aa_end": null,
"aa_length": 123,
"cds_start": 5,
"cds_end": null,
"cds_length": 373,
"cdna_start": 13,
"cdna_end": null,
"cdna_length": 381,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_001304500.2",
"protein_id": "NP_001291429.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 108,
"cds_start": 5,
"cds_end": null,
"cds_length": 327,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2066,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000575744.5",
"protein_id": "ENSP00000459429.1",
"transcript_support_level": 4,
"aa_start": 2,
"aa_end": null,
"aa_length": 108,
"cds_start": 5,
"cds_end": null,
"cds_length": 327,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 565,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_001304498.2",
"protein_id": "NP_001291427.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 104,
"cds_start": 5,
"cds_end": null,
"cds_length": 315,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2127,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000575073.5",
"protein_id": "ENSP00000459804.1",
"transcript_support_level": 2,
"aa_start": 2,
"aa_end": null,
"aa_length": 104,
"cds_start": 5,
"cds_end": null,
"cds_length": 315,
"cdna_start": 45,
"cdna_end": null,
"cdna_length": 530,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "NM_001304497.2",
"protein_id": "NP_001291426.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 100,
"cds_start": 5,
"cds_end": null,
"cds_length": 303,
"cdna_start": 23,
"cdna_end": null,
"cdna_length": 2042,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val",
"transcript": "ENST00000573968.5",
"protein_id": "ENSP00000460312.1",
"transcript_support_level": 2,
"aa_start": 2,
"aa_end": null,
"aa_length": 100,
"cds_start": 5,
"cds_end": null,
"cds_length": 303,
"cdna_start": 22,
"cdna_end": null,
"cdna_length": 2039,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "n.5C>T",
"hgvs_p": null,
"transcript": "ENST00000572415.5",
"protein_id": "ENSP00000460592.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 796,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "n.5C>T",
"hgvs_p": null,
"transcript": "ENST00000573087.5",
"protein_id": "ENSP00000458159.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 851,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "n.23C>T",
"hgvs_p": null,
"transcript": "NR_130755.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2179,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "n.23C>T",
"hgvs_p": null,
"transcript": "NR_130756.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2364,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"hgvs_c": "n.23C>T",
"hgvs_p": null,
"transcript": "NR_130757.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1981,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CEP20",
"gene_hgnc_id": 26435,
"dbsnp": "rs775219497",
"frequency_reference_population": 0.00005452367,
"hom_count_reference_population": 0,
"allele_count_reference_population": 88,
"gnomad_exomes_af": 0.00005541,
"gnomad_genomes_af": 0.0000460078,
"gnomad_exomes_ac": 81,
"gnomad_genomes_ac": 7,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.586579442024231,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.132,
"revel_prediction": "Benign",
"alphamissense_score": 0.8213,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.06,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 6.968,
"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": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_144600.4",
"gene_symbol": "CEP20",
"hgnc_id": 26435,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.5C>T",
"hgvs_p": "p.Ala2Val"
}
],
"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
}