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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: 17-3659974-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=3659974&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 3659974,
"ref": "C",
"alt": "T",
"effect": "splice_region_variant,synonymous_variant",
"transcript": "ENST00000046640.9",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "NM_004937.3",
"protein_id": "NP_004928.2",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 367,
"cds_start": 969,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 1270,
"cdna_end": null,
"cdna_length": 4139,
"mane_select": "ENST00000046640.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "ENST00000046640.9",
"protein_id": "ENSP00000046640.4",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 367,
"cds_start": 969,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 1270,
"cdna_end": null,
"cdna_length": 4139,
"mane_select": "NM_004937.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "ENST00000381870.8",
"protein_id": "ENSP00000371294.3",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 400,
"cds_start": 969,
"cds_end": null,
"cds_length": 1203,
"cdna_start": 1448,
"cdna_end": null,
"cdna_length": 2490,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "NM_001031681.3",
"protein_id": "NP_001026851.2",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 400,
"cds_start": 969,
"cds_end": null,
"cds_length": 1203,
"cdna_start": 1448,
"cdna_end": null,
"cdna_length": 4051,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "NM_001374492.1",
"protein_id": "NP_001361421.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 400,
"cds_start": 969,
"cds_end": null,
"cds_length": 1203,
"cdna_start": 1270,
"cdna_end": null,
"cdna_length": 3873,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "ENST00000673965.1",
"protein_id": "ENSP00000500995.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 367,
"cds_start": 969,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 1443,
"cdna_end": null,
"cdna_length": 2657,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "ENST00000574776.6",
"protein_id": "ENSP00000461118.2",
"transcript_support_level": 4,
"aa_start": 176,
"aa_end": null,
"aa_length": 253,
"cds_start": 528,
"cds_end": null,
"cds_length": 762,
"cdna_start": 1033,
"cdna_end": null,
"cdna_length": 1570,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "NM_001374493.1",
"protein_id": "NP_001361422.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 220,
"cds_start": 528,
"cds_end": null,
"cds_length": 663,
"cdna_start": 1185,
"cdna_end": null,
"cdna_length": 4054,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "NM_001374494.1",
"protein_id": "NP_001361423.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 220,
"cds_start": 528,
"cds_end": null,
"cds_length": 663,
"cdna_start": 1190,
"cdna_end": null,
"cdna_length": 4059,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "NM_001374495.1",
"protein_id": "NP_001361424.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 220,
"cds_start": 528,
"cds_end": null,
"cds_length": 663,
"cdna_start": 1106,
"cdna_end": null,
"cdna_length": 3975,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "NM_001374496.1",
"protein_id": "NP_001361425.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 220,
"cds_start": 528,
"cds_end": null,
"cds_length": 663,
"cdna_start": 1105,
"cdna_end": null,
"cdna_length": 3974,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "ENST00000673669.1",
"protein_id": "ENSP00000501123.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 220,
"cds_start": 528,
"cds_end": null,
"cds_length": 663,
"cdna_start": 1139,
"cdna_end": null,
"cdna_length": 2417,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.216C>T",
"hgvs_p": "p.Asn72Asn",
"transcript": "ENST00000488623.6",
"protein_id": "ENSP00000501016.1",
"transcript_support_level": 3,
"aa_start": 72,
"aa_end": null,
"aa_length": 116,
"cds_start": 216,
"cds_end": null,
"cds_length": 351,
"cdna_start": 1185,
"cdna_end": null,
"cdna_length": 2322,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "XM_006721463.4",
"protein_id": "XP_006721526.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 400,
"cds_start": 969,
"cds_end": null,
"cds_length": 1203,
"cdna_start": 1443,
"cdna_end": null,
"cdna_length": 4046,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn",
"transcript": "XM_011523691.3",
"protein_id": "XP_011521993.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 400,
"cds_start": 969,
"cds_end": null,
"cds_length": 1203,
"cdna_start": 1326,
"cdna_end": null,
"cdna_length": 3929,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.528C>T",
"hgvs_p": "p.Asn176Asn",
"transcript": "XM_011523692.3",
"protein_id": "XP_011521994.1",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 253,
"cds_start": 528,
"cds_end": null,
"cds_length": 762,
"cdna_start": 1190,
"cdna_end": null,
"cdna_length": 3793,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "c.*1754C>T",
"hgvs_p": null,
"transcript": "XM_047435501.1",
"protein_id": "XP_047291457.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 298,
"cds_start": -4,
"cds_end": null,
"cds_length": 897,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2825,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"hgvs_c": "n.*24C>T",
"hgvs_p": null,
"transcript": "XR_007065277.1",
"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": 2579,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CTNS",
"gene_hgnc_id": 2518,
"dbsnp": "rs121908128",
"frequency_reference_population": 0.00015077958,
"hom_count_reference_population": 0,
"allele_count_reference_population": 243,
"gnomad_exomes_af": 0.0000822326,
"gnomad_genomes_af": 0.000807362,
"gnomad_exomes_ac": 120,
"gnomad_genomes_ac": 123,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.699999988079071,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.02199999988079071,
"splice_prediction_selected": "Benign",
"splice_source_selected": "dbscSNV1_RF",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.7,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.895,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": 0.000241968265229104,
"dbscsnv_ada_prediction": "Benign",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -10,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BP7,BS1",
"acmg_by_gene": [
{
"score": -10,
"benign_score": 10,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BP7",
"BS1"
],
"verdict": "Benign",
"transcript": "ENST00000046640.9",
"gene_symbol": "CTNS",
"hgnc_id": 2518,
"effects": [
"splice_region_variant",
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.969C>T",
"hgvs_p": "p.Asn323Asn"
}
],
"clinvar_disease": "Cystinosis,Inborn genetic diseases,Juvenile nephropathic cystinosis,Ocular cystinosis,not provided",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:1 LB:1",
"phenotype_combined": "not provided|Ocular cystinosis;Juvenile nephropathic cystinosis;Inborn genetic diseases|Cystinosis",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}