← Back to variant description
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: 1-225921232-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=225921232&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 225921232,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_013328.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.773T>A",
"hgvs_p": "p.Val258Asp",
"transcript": "NM_013328.4",
"protein_id": "NP_037460.2",
"transcript_support_level": null,
"aa_start": 258,
"aa_end": null,
"aa_length": 320,
"cds_start": 773,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000343818.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_013328.4"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.773T>A",
"hgvs_p": "p.Val258Asp",
"transcript": "ENST00000343818.11",
"protein_id": "ENSP00000342502.6",
"transcript_support_level": 1,
"aa_start": 258,
"aa_end": null,
"aa_length": 320,
"cds_start": 773,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_013328.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000343818.11"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000255835",
"gene_hgnc_id": null,
"hgvs_c": "c.551T>A",
"hgvs_p": "p.Val184Asp",
"transcript": "ENST00000432920.2",
"protein_id": "ENSP00000414068.2",
"transcript_support_level": 2,
"aa_start": 184,
"aa_end": null,
"aa_length": 359,
"cds_start": 551,
"cds_end": null,
"cds_length": 1080,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000432920.2"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.770T>A",
"hgvs_p": "p.Val257Asp",
"transcript": "ENST00000872062.1",
"protein_id": "ENSP00000542121.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 319,
"cds_start": 770,
"cds_end": null,
"cds_length": 960,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872062.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.770T>A",
"hgvs_p": "p.Val257Asp",
"transcript": "ENST00000872065.1",
"protein_id": "ENSP00000542124.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 319,
"cds_start": 770,
"cds_end": null,
"cds_length": 960,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872065.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.767T>A",
"hgvs_p": "p.Val256Asp",
"transcript": "ENST00000931949.1",
"protein_id": "ENSP00000602007.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 318,
"cds_start": 767,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931949.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.704T>A",
"hgvs_p": "p.Val235Asp",
"transcript": "ENST00000931947.1",
"protein_id": "ENSP00000602005.1",
"transcript_support_level": null,
"aa_start": 235,
"aa_end": null,
"aa_length": 297,
"cds_start": 704,
"cds_end": null,
"cds_length": 894,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931947.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.698T>A",
"hgvs_p": "p.Val233Asp",
"transcript": "ENST00000872071.1",
"protein_id": "ENSP00000542130.1",
"transcript_support_level": null,
"aa_start": 233,
"aa_end": null,
"aa_length": 295,
"cds_start": 698,
"cds_end": null,
"cds_length": 888,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872071.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.680T>A",
"hgvs_p": "p.Val227Asp",
"transcript": "ENST00000872063.1",
"protein_id": "ENSP00000542122.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 289,
"cds_start": 680,
"cds_end": null,
"cds_length": 870,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872063.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.677T>A",
"hgvs_p": "p.Val226Asp",
"transcript": "ENST00000954487.1",
"protein_id": "ENSP00000624546.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 288,
"cds_start": 677,
"cds_end": null,
"cds_length": 867,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954487.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.677T>A",
"hgvs_p": "p.Val226Asp",
"transcript": "ENST00000954488.1",
"protein_id": "ENSP00000624547.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 288,
"cds_start": 677,
"cds_end": null,
"cds_length": 867,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000954488.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.593T>A",
"hgvs_p": "p.Val198Asp",
"transcript": "ENST00000872068.1",
"protein_id": "ENSP00000542128.1",
"transcript_support_level": null,
"aa_start": 198,
"aa_end": null,
"aa_length": 260,
"cds_start": 593,
"cds_end": null,
"cds_length": 783,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872068.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.551T>A",
"hgvs_p": "p.Val184Asp",
"transcript": "NM_001271681.2",
"protein_id": "NP_001258610.1",
"transcript_support_level": null,
"aa_start": 184,
"aa_end": null,
"aa_length": 246,
"cds_start": 551,
"cds_end": null,
"cds_length": 741,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001271681.2"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.551T>A",
"hgvs_p": "p.Val184Asp",
"transcript": "ENST00000612039.4",
"protein_id": "ENSP00000478165.1",
"transcript_support_level": 3,
"aa_start": 184,
"aa_end": null,
"aa_length": 246,
"cds_start": 551,
"cds_end": null,
"cds_length": 741,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000612039.4"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.458T>A",
"hgvs_p": "p.Val153Asp",
"transcript": "ENST00000872070.1",
"protein_id": "ENSP00000542129.1",
"transcript_support_level": null,
"aa_start": 153,
"aa_end": null,
"aa_length": 215,
"cds_start": 458,
"cds_end": null,
"cds_length": 648,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872070.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.371T>A",
"hgvs_p": "p.Val124Asp",
"transcript": "ENST00000872067.1",
"protein_id": "ENSP00000542125.1",
"transcript_support_level": null,
"aa_start": 124,
"aa_end": null,
"aa_length": 186,
"cds_start": 371,
"cds_end": null,
"cds_length": 561,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000872067.1"
},
{
"aa_ref": "V",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "c.278T>A",
"hgvs_p": "p.Val93Asp",
"transcript": "ENST00000931948.1",
"protein_id": "ENSP00000602006.1",
"transcript_support_level": null,
"aa_start": 93,
"aa_end": null,
"aa_length": 155,
"cds_start": 278,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931948.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "n.1331T>A",
"hgvs_p": null,
"transcript": "ENST00000446534.1",
"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": "ENST00000446534.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "n.490T>A",
"hgvs_p": null,
"transcript": "ENST00000466127.1",
"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": "ENST00000466127.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"hgvs_c": "n.2382T>A",
"hgvs_p": null,
"transcript": "ENST00000478402.5",
"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": "ENST00000478402.5"
}
],
"gene_symbol": "PYCR2",
"gene_hgnc_id": 30262,
"dbsnp": "rs886037932",
"frequency_reference_population": 0.0000013682829,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000136828,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9580621719360352,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.854,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9955,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.21,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.342,
"phylop100way_prediction": "Uncertain_significance",
"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": "PM2,PM5,PP2,PP3_Strong",
"acmg_by_gene": [
{
"score": 9,
"benign_score": 0,
"pathogenic_score": 9,
"criteria": [
"PM2",
"PM5",
"PP2",
"PP3_Strong"
],
"verdict": "Likely_pathogenic",
"transcript": "NM_013328.4",
"gene_symbol": "PYCR2",
"hgnc_id": 30262,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.773T>A",
"hgvs_p": "p.Val258Asp"
},
{
"score": 8,
"benign_score": 0,
"pathogenic_score": 8,
"criteria": [
"PM2",
"PM5",
"PP3_Strong"
],
"verdict": "Likely_pathogenic",
"transcript": "ENST00000432920.2",
"gene_symbol": "ENSG00000255835",
"hgnc_id": null,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.551T>A",
"hgvs_p": "p.Val184Asp"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}