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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: 4-127898523-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=127898523&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 127898523,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "NM_001441357.1",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2895G>A",
"hgvs_p": "p.Pro965Pro",
"transcript": "NM_014264.5",
"protein_id": "NP_055079.3",
"transcript_support_level": null,
"aa_start": 965,
"aa_end": null,
"aa_length": 970,
"cds_start": 2895,
"cds_end": null,
"cds_length": 2913,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000270861.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014264.5"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2895G>A",
"hgvs_p": "p.Pro965Pro",
"transcript": "ENST00000270861.10",
"protein_id": "ENSP00000270861.5",
"transcript_support_level": 1,
"aa_start": 965,
"aa_end": null,
"aa_length": 970,
"cds_start": 2895,
"cds_end": null,
"cds_length": 2913,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014264.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000270861.10"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2898G>A",
"hgvs_p": "p.Pro966Pro",
"transcript": "NM_001441357.1",
"protein_id": "NP_001428286.1",
"transcript_support_level": null,
"aa_start": 966,
"aa_end": null,
"aa_length": 971,
"cds_start": 2898,
"cds_end": null,
"cds_length": 2916,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441357.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2799G>A",
"hgvs_p": "p.Pro933Pro",
"transcript": "NM_001190799.2",
"protein_id": "NP_001177728.1",
"transcript_support_level": null,
"aa_start": 933,
"aa_end": null,
"aa_length": 938,
"cds_start": 2799,
"cds_end": null,
"cds_length": 2817,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001190799.2"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2799G>A",
"hgvs_p": "p.Pro933Pro",
"transcript": "ENST00000513090.5",
"protein_id": "ENSP00000427554.1",
"transcript_support_level": 2,
"aa_start": 933,
"aa_end": null,
"aa_length": 938,
"cds_start": 2799,
"cds_end": null,
"cds_length": 2817,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000513090.5"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2796G>A",
"hgvs_p": "p.Pro932Pro",
"transcript": "NM_001441358.1",
"protein_id": "NP_001428287.1",
"transcript_support_level": null,
"aa_start": 932,
"aa_end": null,
"aa_length": 937,
"cds_start": 2796,
"cds_end": null,
"cds_length": 2814,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441358.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2793G>A",
"hgvs_p": "p.Pro931Pro",
"transcript": "NM_001441359.1",
"protein_id": "NP_001428288.1",
"transcript_support_level": null,
"aa_start": 931,
"aa_end": null,
"aa_length": 936,
"cds_start": 2793,
"cds_end": null,
"cds_length": 2811,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441359.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2793G>A",
"hgvs_p": "p.Pro931Pro",
"transcript": "ENST00000852980.1",
"protein_id": "ENSP00000523039.1",
"transcript_support_level": null,
"aa_start": 931,
"aa_end": null,
"aa_length": 936,
"cds_start": 2793,
"cds_end": null,
"cds_length": 2811,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000852980.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2772G>A",
"hgvs_p": "p.Pro924Pro",
"transcript": "NM_001190801.2",
"protein_id": "NP_001177730.1",
"transcript_support_level": null,
"aa_start": 924,
"aa_end": null,
"aa_length": 929,
"cds_start": 2772,
"cds_end": null,
"cds_length": 2790,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001190801.2"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2772G>A",
"hgvs_p": "p.Pro924Pro",
"transcript": "ENST00000514379.5",
"protein_id": "ENSP00000423582.1",
"transcript_support_level": 2,
"aa_start": 924,
"aa_end": null,
"aa_length": 929,
"cds_start": 2772,
"cds_end": null,
"cds_length": 2790,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000514379.5"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2754G>A",
"hgvs_p": "p.Pro918Pro",
"transcript": "NM_001441360.1",
"protein_id": "NP_001428289.1",
"transcript_support_level": null,
"aa_start": 918,
"aa_end": null,
"aa_length": 923,
"cds_start": 2754,
"cds_end": null,
"cds_length": 2772,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441360.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2712G>A",
"hgvs_p": "p.Pro904Pro",
"transcript": "ENST00000507249.5",
"protein_id": "ENSP00000423412.1",
"transcript_support_level": 5,
"aa_start": 904,
"aa_end": null,
"aa_length": 909,
"cds_start": 2712,
"cds_end": null,
"cds_length": 2730,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000507249.5"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2697G>A",
"hgvs_p": "p.Pro899Pro",
"transcript": "NM_001441361.1",
"protein_id": "NP_001428290.1",
"transcript_support_level": null,
"aa_start": 899,
"aa_end": null,
"aa_length": 904,
"cds_start": 2697,
"cds_end": null,
"cds_length": 2715,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441361.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2676G>A",
"hgvs_p": "p.Pro892Pro",
"transcript": "NM_001441362.1",
"protein_id": "NP_001428291.1",
"transcript_support_level": null,
"aa_start": 892,
"aa_end": null,
"aa_length": 897,
"cds_start": 2676,
"cds_end": null,
"cds_length": 2694,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441362.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2670G>A",
"hgvs_p": "p.Pro890Pro",
"transcript": "NM_001441366.1",
"protein_id": "NP_001428295.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 895,
"cds_start": 2670,
"cds_end": null,
"cds_length": 2688,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441366.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2661G>A",
"hgvs_p": "p.Pro887Pro",
"transcript": "ENST00000515069.5",
"protein_id": "ENSP00000421774.1",
"transcript_support_level": 5,
"aa_start": 887,
"aa_end": null,
"aa_length": 892,
"cds_start": 2661,
"cds_end": null,
"cds_length": 2679,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000515069.5"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2652G>A",
"hgvs_p": "p.Pro884Pro",
"transcript": "NM_001441367.1",
"protein_id": "NP_001428296.1",
"transcript_support_level": null,
"aa_start": 884,
"aa_end": null,
"aa_length": 889,
"cds_start": 2652,
"cds_end": null,
"cds_length": 2670,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441367.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2625G>A",
"hgvs_p": "p.Pro875Pro",
"transcript": "NM_001441368.1",
"protein_id": "NP_001428297.1",
"transcript_support_level": null,
"aa_start": 875,
"aa_end": null,
"aa_length": 880,
"cds_start": 2625,
"cds_end": null,
"cds_length": 2643,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441368.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2574G>A",
"hgvs_p": "p.Pro858Pro",
"transcript": "NM_001441369.1",
"protein_id": "NP_001428298.1",
"transcript_support_level": null,
"aa_start": 858,
"aa_end": null,
"aa_length": 863,
"cds_start": 2574,
"cds_end": null,
"cds_length": 2592,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441369.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.2274G>A",
"hgvs_p": "p.Pro758Pro",
"transcript": "NM_001441371.1",
"protein_id": "NP_001428300.1",
"transcript_support_level": null,
"aa_start": 758,
"aa_end": null,
"aa_length": 763,
"cds_start": 2274,
"cds_end": null,
"cds_length": 2292,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441371.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "n.792G>A",
"hgvs_p": null,
"transcript": "ENST00000510192.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000510192.1"
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"hgvs_c": "c.*37G>A",
"hgvs_p": null,
"transcript": "ENST00000508113.1",
"protein_id": "ENSP00000427568.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 197,
"cds_start": null,
"cds_end": null,
"cds_length": 596,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000508113.1"
}
],
"gene_symbol": "PLK4",
"gene_hgnc_id": 11397,
"dbsnp": "rs6820138",
"frequency_reference_population": 0.00058372127,
"hom_count_reference_population": 7,
"allele_count_reference_population": 888,
"gnomad_exomes_af": 0.000304563,
"gnomad_genomes_af": 0.00309665,
"gnomad_exomes_ac": 417,
"gnomad_genomes_ac": 471,
"gnomad_exomes_homalt": 3,
"gnomad_genomes_homalt": 4,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.800000011920929,
"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": -0.8,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.008,
"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": -21,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
"acmg_by_gene": [
{
"score": -21,
"benign_score": 21,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001441357.1",
"gene_symbol": "PLK4",
"hgnc_id": 11397,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2898G>A",
"hgvs_p": "p.Pro966Pro"
}
],
"clinvar_disease": "not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not specified|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}