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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: 20-59865590-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=59865590&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "20",
"pos": 59865590,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_014258.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala",
"transcript": "NM_014258.4",
"protein_id": "NP_055073.2",
"transcript_support_level": null,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1530,
"cds_start": 4441,
"cds_end": null,
"cds_length": 4593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000357552.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014258.4"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala",
"transcript": "ENST00000357552.8",
"protein_id": "ENSP00000350162.2",
"transcript_support_level": 1,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1530,
"cds_start": 4441,
"cds_end": null,
"cds_length": 4593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014258.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000357552.8"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 44,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala",
"transcript": "ENST00000371001.6",
"protein_id": "ENSP00000360040.2",
"transcript_support_level": 1,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1530,
"cds_start": 4441,
"cds_end": null,
"cds_length": 4593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000371001.6"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.499A>G",
"hgvs_p": "p.Thr167Ala",
"transcript": "ENST00000412613.1",
"protein_id": "ENSP00000404358.1",
"transcript_support_level": 3,
"aa_start": 167,
"aa_end": null,
"aa_length": 207,
"cds_start": 499,
"cds_end": null,
"cds_length": 625,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000412613.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4462A>G",
"hgvs_p": "p.Thr1488Ala",
"transcript": "XM_011528487.4",
"protein_id": "XP_011526789.1",
"transcript_support_level": null,
"aa_start": 1488,
"aa_end": null,
"aa_length": 1537,
"cds_start": 4462,
"cds_end": null,
"cds_length": 4614,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528487.4"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4462A>G",
"hgvs_p": "p.Thr1488Ala",
"transcript": "XM_011528488.3",
"protein_id": "XP_011526790.1",
"transcript_support_level": null,
"aa_start": 1488,
"aa_end": null,
"aa_length": 1537,
"cds_start": 4462,
"cds_end": null,
"cds_length": 4614,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528488.3"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 44,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4462A>G",
"hgvs_p": "p.Thr1488Ala",
"transcript": "XM_017027586.2",
"protein_id": "XP_016883075.1",
"transcript_support_level": null,
"aa_start": 1488,
"aa_end": null,
"aa_length": 1537,
"cds_start": 4462,
"cds_end": null,
"cds_length": 4614,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017027586.2"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4459A>G",
"hgvs_p": "p.Thr1487Ala",
"transcript": "XM_017027587.2",
"protein_id": "XP_016883076.1",
"transcript_support_level": null,
"aa_start": 1487,
"aa_end": null,
"aa_length": 1536,
"cds_start": 4459,
"cds_end": null,
"cds_length": 4611,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017027587.2"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala",
"transcript": "XM_011528489.3",
"protein_id": "XP_011526791.1",
"transcript_support_level": null,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1530,
"cds_start": 4441,
"cds_end": null,
"cds_length": 4593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528489.3"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 44,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala",
"transcript": "XM_047439825.1",
"protein_id": "XP_047295781.1",
"transcript_support_level": null,
"aa_start": 1481,
"aa_end": null,
"aa_length": 1530,
"cds_start": 4441,
"cds_end": null,
"cds_length": 4593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439825.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4438A>G",
"hgvs_p": "p.Thr1480Ala",
"transcript": "XM_011528490.4",
"protein_id": "XP_011526792.1",
"transcript_support_level": null,
"aa_start": 1480,
"aa_end": null,
"aa_length": 1529,
"cds_start": 4438,
"cds_end": null,
"cds_length": 4590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528490.4"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 44,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4306A>G",
"hgvs_p": "p.Thr1436Ala",
"transcript": "XM_047439826.1",
"protein_id": "XP_047295782.1",
"transcript_support_level": null,
"aa_start": 1436,
"aa_end": null,
"aa_length": 1485,
"cds_start": 4306,
"cds_end": null,
"cds_length": 4458,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439826.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 44,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4291A>G",
"hgvs_p": "p.Thr1431Ala",
"transcript": "XM_047439827.1",
"protein_id": "XP_047295783.1",
"transcript_support_level": null,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1480,
"cds_start": 4291,
"cds_end": null,
"cds_length": 4443,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439827.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.4135A>G",
"hgvs_p": "p.Thr1379Ala",
"transcript": "XM_047439828.1",
"protein_id": "XP_047295784.1",
"transcript_support_level": null,
"aa_start": 1379,
"aa_end": null,
"aa_length": 1428,
"cds_start": 4135,
"cds_end": null,
"cds_length": 4287,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439828.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"hgvs_c": "c.3946A>G",
"hgvs_p": "p.Thr1316Ala",
"transcript": "XM_047439829.1",
"protein_id": "XP_047295785.1",
"transcript_support_level": null,
"aa_start": 1316,
"aa_end": null,
"aa_length": 1365,
"cds_start": 3946,
"cds_end": null,
"cds_length": 4098,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439829.1"
}
],
"gene_symbol": "SYCP2",
"gene_hgnc_id": 11490,
"dbsnp": "rs374889210",
"frequency_reference_population": 0.00002743775,
"hom_count_reference_population": 0,
"allele_count_reference_population": 44,
"gnomad_exomes_af": 0.0000151544,
"gnomad_genomes_af": 0.000144824,
"gnomad_exomes_ac": 22,
"gnomad_genomes_ac": 22,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.026291459798812866,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.013,
"revel_prediction": "Benign",
"alphamissense_score": 0.0826,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.65,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.163,
"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": -8,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BS2",
"acmg_by_gene": [
{
"score": -8,
"benign_score": 8,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_014258.4",
"gene_symbol": "SYCP2",
"hgnc_id": 11490,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.4441A>G",
"hgvs_p": "p.Thr1481Ala"
}
],
"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
}