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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: 19-8321536-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=8321536&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 8321536,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_001031.5",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "NM_001031.5",
"protein_id": "NP_001022.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 41,
"cdna_end": null,
"cdna_length": 1330,
"mane_select": "ENST00000600659.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001031.5"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000600659.3",
"protein_id": "ENSP00000472469.1",
"transcript_support_level": 1,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 41,
"cdna_end": null,
"cdna_length": 1330,
"mane_select": "NM_001031.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000600659.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "n.42C>T",
"hgvs_p": null,
"transcript": "ENST00000602140.1",
"protein_id": null,
"transcript_support_level": 1,
"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": 912,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000602140.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000930317.1",
"protein_id": "ENSP00000600376.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 229,
"cdna_end": null,
"cdna_length": 574,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930317.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000948366.1",
"protein_id": "ENSP00000618425.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 37,
"cdna_end": null,
"cdna_length": 1733,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948366.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000948367.1",
"protein_id": "ENSP00000618426.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 38,
"cdna_end": null,
"cdna_length": 1325,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948367.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000930316.1",
"protein_id": "ENSP00000600375.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 66,
"cds_start": 6,
"cds_end": null,
"cds_length": 201,
"cdna_start": 49,
"cdna_end": null,
"cdna_length": 1324,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930316.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "ENST00000930315.1",
"protein_id": "ENSP00000600374.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 53,
"cds_start": 6,
"cds_end": null,
"cds_length": 162,
"cdna_start": 76,
"cdna_end": null,
"cdna_length": 1317,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930315.1"
},
{
"aa_ref": "D",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp",
"transcript": "XM_047439201.1",
"protein_id": "XP_047295157.1",
"transcript_support_level": null,
"aa_start": 2,
"aa_end": null,
"aa_length": 69,
"cds_start": 6,
"cds_end": null,
"cds_length": 210,
"cdna_start": 41,
"cdna_end": null,
"cdna_length": 267,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047439201.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "n.379C>T",
"hgvs_p": null,
"transcript": "ENST00000449223.3",
"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": 1523,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000449223.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "c.-178G>A",
"hgvs_p": null,
"transcript": "NM_005001.5",
"protein_id": "NP_004992.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 113,
"cds_start": null,
"cds_end": null,
"cds_length": 342,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 580,
"mane_select": "ENST00000301457.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005001.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "c.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000301457.3",
"protein_id": "ENSP00000301457.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 113,
"cds_start": null,
"cds_end": null,
"cds_length": 342,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 580,
"mane_select": "NM_005001.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000301457.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000167774",
"gene_hgnc_id": null,
"hgvs_c": "n.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000598884.1",
"protein_id": "ENSP00000470609.1",
"transcript_support_level": 4,
"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": 580,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000598884.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "c.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000930188.1",
"protein_id": "ENSP00000600247.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 144,
"cds_start": null,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 604,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930188.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "c.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000870893.1",
"protein_id": "ENSP00000540952.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 63,
"cds_start": null,
"cds_end": null,
"cds_length": 192,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 360,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000870893.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"hgvs_c": "n.-98C>T",
"hgvs_p": null,
"transcript": "ENST00000417088.2",
"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": 334,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000417088.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "n.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000593729.5",
"protein_id": "ENSP00000470962.1",
"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": 569,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000593729.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "n.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000595856.5",
"protein_id": "ENSP00000471943.1",
"transcript_support_level": 5,
"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": 553,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000595856.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "n.-178G>A",
"hgvs_p": null,
"transcript": "ENST00000601101.5",
"protein_id": "ENSP00000471333.1",
"transcript_support_level": 4,
"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": 414,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000601101.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFA7",
"gene_hgnc_id": 7691,
"hgvs_c": "n.-161G>A",
"hgvs_p": null,
"transcript": "NR_135539.2",
"protein_id": null,
"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": 742,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_135539.2"
}
],
"gene_symbol": "RPS28",
"gene_hgnc_id": 10418,
"dbsnp": "rs534143211",
"frequency_reference_population": 0.000043464566,
"hom_count_reference_population": 0,
"allele_count_reference_population": 69,
"gnomad_exomes_af": 0.0000390182,
"gnomad_genomes_af": 0.0000853735,
"gnomad_exomes_ac": 56,
"gnomad_genomes_ac": 13,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.4099999964237213,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.41,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.963,
"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": "Benign",
"acmg_criteria": "BP4_Moderate,BP6_Moderate,BP7,BS2",
"acmg_by_gene": [
{
"score": -9,
"benign_score": 9,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Moderate",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001031.5",
"gene_symbol": "RPS28",
"hgnc_id": 10418,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.6C>T",
"hgvs_p": "p.Asp2Asp"
},
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_005001.5",
"gene_symbol": "NDUFA7",
"hgnc_id": 7691,
"effects": [
"upstream_gene_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.-178G>A",
"hgvs_p": null
},
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000598884.1",
"gene_symbol": "ENSG00000167774",
"hgnc_id": null,
"effects": [
"upstream_gene_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.-178G>A",
"hgvs_p": null
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}