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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: 11-2583467-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=2583467&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 2583467,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_000218.3",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.954G>C",
"hgvs_p": "p.Lys318Asn",
"transcript": "NM_000218.3",
"protein_id": "NP_000209.2",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 676,
"cds_start": 954,
"cds_end": null,
"cds_length": 2031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000155840.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000218.3"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.954G>C",
"hgvs_p": "p.Lys318Asn",
"transcript": "ENST00000155840.12",
"protein_id": "ENSP00000155840.2",
"transcript_support_level": 1,
"aa_start": 318,
"aa_end": null,
"aa_length": 676,
"cds_start": 954,
"cds_end": null,
"cds_length": 2031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000218.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000155840.12"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.573G>C",
"hgvs_p": "p.Lys191Asn",
"transcript": "ENST00000335475.6",
"protein_id": "ENSP00000334497.5",
"transcript_support_level": 1,
"aa_start": 191,
"aa_end": null,
"aa_length": 549,
"cds_start": 573,
"cds_end": null,
"cds_length": 1650,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000335475.6"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.951G>C",
"hgvs_p": "p.Lys317Asn",
"transcript": "ENST00000910997.1",
"protein_id": "ENSP00000581056.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 675,
"cds_start": 951,
"cds_end": null,
"cds_length": 2028,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000910997.1"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.954G>C",
"hgvs_p": "p.Lys318Asn",
"transcript": "NM_001406836.1",
"protein_id": "NP_001393765.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 644,
"cds_start": 954,
"cds_end": null,
"cds_length": 1935,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001406836.1"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.813G>C",
"hgvs_p": "p.Lys271Asn",
"transcript": "ENST00000713725.1",
"protein_id": "ENSP00000519029.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 629,
"cds_start": 813,
"cds_end": null,
"cds_length": 1890,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713725.1"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.684G>C",
"hgvs_p": "p.Lys228Asn",
"transcript": "NM_001406837.1",
"protein_id": "NP_001393766.1",
"transcript_support_level": null,
"aa_start": 228,
"aa_end": null,
"aa_length": 586,
"cds_start": 684,
"cds_end": null,
"cds_length": 1761,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001406837.1"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.693G>C",
"hgvs_p": "p.Lys231Asn",
"transcript": "ENST00000496887.7",
"protein_id": "ENSP00000434560.2",
"transcript_support_level": 5,
"aa_start": 231,
"aa_end": null,
"aa_length": 557,
"cds_start": 693,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000496887.7"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.573G>C",
"hgvs_p": "p.Lys191Asn",
"transcript": "NM_181798.2",
"protein_id": "NP_861463.1",
"transcript_support_level": null,
"aa_start": 191,
"aa_end": null,
"aa_length": 549,
"cds_start": 573,
"cds_end": null,
"cds_length": 1650,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_181798.2"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.510G>C",
"hgvs_p": "p.Lys170Asn",
"transcript": "NM_001406838.1",
"protein_id": "NP_001393767.1",
"transcript_support_level": null,
"aa_start": 170,
"aa_end": null,
"aa_length": 496,
"cds_start": 510,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001406838.1"
},
{
"aa_ref": "K",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "c.510G>C",
"hgvs_p": "p.Lys170Asn",
"transcript": "ENST00000646564.2",
"protein_id": "ENSP00000495806.2",
"transcript_support_level": null,
"aa_start": 170,
"aa_end": null,
"aa_length": 428,
"cds_start": 510,
"cds_end": null,
"cds_length": 1287,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000646564.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "n.*920G>C",
"hgvs_p": null,
"transcript": "ENST00000713724.1",
"protein_id": "ENSP00000519028.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000713724.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"hgvs_c": "n.*920G>C",
"hgvs_p": null,
"transcript": "ENST00000713724.1",
"protein_id": "ENSP00000519028.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000713724.1"
}
],
"gene_symbol": "KCNQ1",
"gene_hgnc_id": 6294,
"dbsnp": "rs199472752",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9771630167961121,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "CardioboostArm",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.737,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9296,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.15,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 0.271,
"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": 9,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PM1,PM2,PP2,PP3_Strong",
"acmg_by_gene": [
{
"score": 9,
"benign_score": 0,
"pathogenic_score": 9,
"criteria": [
"PM1",
"PM2",
"PP2",
"PP3_Strong"
],
"verdict": "Likely_pathogenic",
"transcript": "NM_000218.3",
"gene_symbol": "KCNQ1",
"hgnc_id": 6294,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.954G>C",
"hgvs_p": "p.Lys318Asn"
}
],
"clinvar_disease": "Congenital long QT syndrome,not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1 O:1",
"phenotype_combined": "Congenital long QT syndrome|not provided",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}