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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: 4-95104504-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=95104504&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 95104504,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000515059.6",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "NM_001203.3",
"protein_id": "NP_001194.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 376,
"cdna_end": null,
"cdna_length": 5580,
"mane_select": "ENST00000515059.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000515059.6",
"protein_id": "ENSP00000426617.1",
"transcript_support_level": 1,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 376,
"cdna_end": null,
"cdna_length": 5580,
"mane_select": "NM_001203.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000394931.1",
"protein_id": "ENSP00000378389.1",
"transcript_support_level": 1,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 150,
"cdna_end": null,
"cdna_length": 1922,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000512312.5",
"protein_id": "ENSP00000425444.1",
"transcript_support_level": 1,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 250,
"cdna_end": null,
"cdna_length": 1679,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.170C>G",
"hgvs_p": "p.Pro57Arg",
"transcript": "NM_001256793.2",
"protein_id": "NP_001243722.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 532,
"cds_start": 170,
"cds_end": null,
"cds_length": 1599,
"cdna_start": 193,
"cdna_end": null,
"cdna_length": 5397,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.170C>G",
"hgvs_p": "p.Pro57Arg",
"transcript": "ENST00000440890.7",
"protein_id": "ENSP00000401907.2",
"transcript_support_level": 2,
"aa_start": 57,
"aa_end": null,
"aa_length": 532,
"cds_start": 170,
"cds_end": null,
"cds_length": 1599,
"cdna_start": 193,
"cdna_end": null,
"cdna_length": 5397,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "NM_001256792.2",
"protein_id": "NP_001243721.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 642,
"cdna_end": null,
"cdna_length": 5846,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "NM_001256794.1",
"protein_id": "NP_001243723.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 234,
"cdna_end": null,
"cdna_length": 5440,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000264568.8",
"protein_id": "ENSP00000264568.4",
"transcript_support_level": 2,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 234,
"cdna_end": null,
"cdna_length": 1807,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000509540.6",
"protein_id": "ENSP00000421671.1",
"transcript_support_level": 2,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 289,
"cdna_end": null,
"cdna_length": 1821,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000672698.1",
"protein_id": "ENSP00000500035.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 428,
"cdna_end": null,
"cdna_length": 4541,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "ENST00000506363.5",
"protein_id": "ENSP00000421144.1",
"transcript_support_level": 4,
"aa_start": 27,
"aa_end": null,
"aa_length": 124,
"cds_start": 80,
"cds_end": null,
"cds_length": 375,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 731,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_011532201.3",
"protein_id": "XP_011530503.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 281,
"cdna_end": null,
"cdna_length": 5487,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_017008558.2",
"protein_id": "XP_016864047.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 419,
"cdna_end": null,
"cdna_length": 5625,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_017008559.2",
"protein_id": "XP_016864048.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 463,
"cdna_end": null,
"cdna_length": 5669,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_017008560.2",
"protein_id": "XP_016864049.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 392,
"cdna_end": null,
"cdna_length": 5598,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_047416091.1",
"protein_id": "XP_047272047.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 605,
"cdna_end": null,
"cdna_length": 5811,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_047416093.1",
"protein_id": "XP_047272049.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 448,
"cdna_end": null,
"cdna_length": 5654,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_047416094.1",
"protein_id": "XP_047272050.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 328,
"cdna_end": null,
"cdna_length": 5534,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg",
"transcript": "XM_047416095.1",
"protein_id": "XP_047272051.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 502,
"cds_start": 80,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 2670,
"cdna_end": null,
"cdna_length": 7876,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"hgvs_c": "n.291C>G",
"hgvs_p": null,
"transcript": "ENST00000502683.6",
"protein_id": null,
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 572,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "BMPR1B",
"gene_hgnc_id": 1077,
"dbsnp": "rs757312834",
"frequency_reference_population": 0.00001177665,
"hom_count_reference_population": 0,
"allele_count_reference_population": 19,
"gnomad_exomes_af": 0.0000123171,
"gnomad_genomes_af": 0.0000065799,
"gnomad_exomes_ac": 18,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.1905384063720703,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.395,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0674,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.06,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 3.398,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000515059.6",
"gene_symbol": "BMPR1B",
"hgnc_id": 1077,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR,Unknown",
"hgvs_c": "c.80C>G",
"hgvs_p": "p.Pro27Arg"
}
],
"clinvar_disease": " 3, primary,Acromesomelic dysplasia 3,Pulmonary hypertension,Type A2 brachydactyly",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "Pulmonary hypertension, primary, 3|Acromesomelic dysplasia 3;Type A2 brachydactyly",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}