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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: 2-97657182-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=97657182&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 97657182,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_005735.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.998C>G",
"hgvs_p": "p.Pro333Arg",
"transcript": "NM_005735.4",
"protein_id": "NP_005726.1",
"transcript_support_level": null,
"aa_start": 333,
"aa_end": null,
"aa_length": 376,
"cds_start": 998,
"cds_end": null,
"cds_length": 1131,
"cdna_start": 1152,
"cdna_end": null,
"cdna_length": 2204,
"mane_select": "ENST00000289228.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005735.4"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.998C>G",
"hgvs_p": "p.Pro333Arg",
"transcript": "ENST00000289228.7",
"protein_id": "ENSP00000289228.5",
"transcript_support_level": 1,
"aa_start": 333,
"aa_end": null,
"aa_length": 376,
"cds_start": 998,
"cds_end": null,
"cds_length": 1131,
"cdna_start": 1152,
"cdna_end": null,
"cdna_length": 2204,
"mane_select": "NM_005735.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000289228.7"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.998C>G",
"hgvs_p": "p.Pro333Arg",
"transcript": "ENST00000855774.1",
"protein_id": "ENSP00000525833.1",
"transcript_support_level": null,
"aa_start": 333,
"aa_end": null,
"aa_length": 387,
"cds_start": 998,
"cds_end": null,
"cds_length": 1164,
"cdna_start": 1152,
"cdna_end": null,
"cdna_length": 2207,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855774.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.1031C>G",
"hgvs_p": "p.Pro344Arg",
"transcript": "ENST00000936776.1",
"protein_id": "ENSP00000606835.1",
"transcript_support_level": null,
"aa_start": 344,
"aa_end": null,
"aa_length": 387,
"cds_start": 1031,
"cds_end": null,
"cds_length": 1164,
"cdna_start": 1149,
"cdna_end": null,
"cdna_length": 2193,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936776.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.1016C>G",
"hgvs_p": "p.Pro339Arg",
"transcript": "ENST00000855778.1",
"protein_id": "ENSP00000525837.1",
"transcript_support_level": null,
"aa_start": 339,
"aa_end": null,
"aa_length": 382,
"cds_start": 1016,
"cds_end": null,
"cds_length": 1149,
"cdna_start": 1086,
"cdna_end": null,
"cdna_length": 2107,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855778.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.995C>G",
"hgvs_p": "p.Pro332Arg",
"transcript": "ENST00000936775.1",
"protein_id": "ENSP00000606834.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 375,
"cds_start": 995,
"cds_end": null,
"cds_length": 1128,
"cdna_start": 1134,
"cdna_end": null,
"cdna_length": 2176,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936775.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.977C>G",
"hgvs_p": "p.Pro326Arg",
"transcript": "ENST00000855775.1",
"protein_id": "ENSP00000525834.1",
"transcript_support_level": null,
"aa_start": 326,
"aa_end": null,
"aa_length": 369,
"cds_start": 977,
"cds_end": null,
"cds_length": 1110,
"cdna_start": 1101,
"cdna_end": null,
"cdna_length": 2144,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855775.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.962C>G",
"hgvs_p": "p.Pro321Arg",
"transcript": "ENST00000855776.1",
"protein_id": "ENSP00000525835.1",
"transcript_support_level": null,
"aa_start": 321,
"aa_end": null,
"aa_length": 364,
"cds_start": 962,
"cds_end": null,
"cds_length": 1095,
"cdna_start": 1093,
"cdna_end": null,
"cdna_length": 2121,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855776.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.890C>G",
"hgvs_p": "p.Pro297Arg",
"transcript": "ENST00000936777.1",
"protein_id": "ENSP00000606836.1",
"transcript_support_level": null,
"aa_start": 297,
"aa_end": null,
"aa_length": 340,
"cds_start": 890,
"cds_end": null,
"cds_length": 1023,
"cdna_start": 1003,
"cdna_end": null,
"cdna_length": 2030,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936777.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.857C>G",
"hgvs_p": "p.Pro286Arg",
"transcript": "ENST00000855773.1",
"protein_id": "ENSP00000525832.1",
"transcript_support_level": null,
"aa_start": 286,
"aa_end": null,
"aa_length": 329,
"cds_start": 857,
"cds_end": null,
"cds_length": 990,
"cdna_start": 1081,
"cdna_end": null,
"cdna_length": 2105,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855773.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.791C>G",
"hgvs_p": "p.Pro264Arg",
"transcript": "ENST00000855777.1",
"protein_id": "ENSP00000525836.1",
"transcript_support_level": null,
"aa_start": 264,
"aa_end": null,
"aa_length": 307,
"cds_start": 791,
"cds_end": null,
"cds_length": 924,
"cdna_start": 906,
"cdna_end": null,
"cdna_length": 1928,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855777.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.656C>G",
"hgvs_p": "p.Pro219Arg",
"transcript": "ENST00000936778.1",
"protein_id": "ENSP00000606837.1",
"transcript_support_level": null,
"aa_start": 219,
"aa_end": null,
"aa_length": 262,
"cds_start": 656,
"cds_end": null,
"cds_length": 789,
"cdna_start": 764,
"cdna_end": null,
"cdna_length": 1786,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936778.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.866C>G",
"hgvs_p": "p.Pro289Arg",
"transcript": "XM_017003116.2",
"protein_id": "XP_016858605.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 332,
"cds_start": 866,
"cds_end": null,
"cds_length": 999,
"cdna_start": 1288,
"cdna_end": null,
"cdna_length": 2340,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017003116.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"hgvs_c": "c.776C>G",
"hgvs_p": "p.Pro259Arg",
"transcript": "XM_005263854.6",
"protein_id": "XP_005263911.1",
"transcript_support_level": null,
"aa_start": 259,
"aa_end": null,
"aa_length": 302,
"cds_start": 776,
"cds_end": null,
"cds_length": 909,
"cdna_start": 1076,
"cdna_end": null,
"cdna_length": 2128,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005263854.6"
}
],
"gene_symbol": "ACTR1B",
"gene_hgnc_id": 168,
"dbsnp": "rs571901265",
"frequency_reference_population": 0.0000020531409,
"hom_count_reference_population": 0,
"allele_count_reference_population": 3,
"gnomad_exomes_af": 0.00000205314,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 3,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9720205068588257,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.539,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.9565,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.14,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.932,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.03,
"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": 6,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PM2,PP3_Strong",
"acmg_by_gene": [
{
"score": 6,
"benign_score": 0,
"pathogenic_score": 6,
"criteria": [
"PM2",
"PP3_Strong"
],
"verdict": "Likely_pathogenic",
"transcript": "NM_005735.4",
"gene_symbol": "ACTR1B",
"hgnc_id": 168,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.998C>G",
"hgvs_p": "p.Pro333Arg"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}