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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: 16-88654746-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=88654746&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 88654746,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_002461.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.959C>T",
"hgvs_p": "p.Ala320Val",
"transcript": "NM_002461.3",
"protein_id": "NP_002452.1",
"transcript_support_level": null,
"aa_start": 320,
"aa_end": null,
"aa_length": 400,
"cds_start": 959,
"cds_end": null,
"cds_length": 1203,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000301012.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002461.3"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.959C>T",
"hgvs_p": "p.Ala320Val",
"transcript": "ENST00000301012.8",
"protein_id": "ENSP00000301012.3",
"transcript_support_level": 1,
"aa_start": 320,
"aa_end": null,
"aa_length": 400,
"cds_start": 959,
"cds_end": null,
"cds_length": 1203,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002461.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000301012.8"
},
{
"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": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "n.1518C>T",
"hgvs_p": null,
"transcript": "ENST00000565149.5",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000565149.5"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.1079C>T",
"hgvs_p": "p.Ala360Val",
"transcript": "ENST00000899622.1",
"protein_id": "ENSP00000569681.1",
"transcript_support_level": null,
"aa_start": 360,
"aa_end": null,
"aa_length": 440,
"cds_start": 1079,
"cds_end": null,
"cds_length": 1323,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899622.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.1076C>T",
"hgvs_p": "p.Ala359Val",
"transcript": "ENST00000960173.1",
"protein_id": "ENSP00000630232.1",
"transcript_support_level": null,
"aa_start": 359,
"aa_end": null,
"aa_length": 439,
"cds_start": 1076,
"cds_end": null,
"cds_length": 1320,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960173.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Ala352Val",
"transcript": "ENST00000960172.1",
"protein_id": "ENSP00000630231.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 432,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1299,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960172.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.956C>T",
"hgvs_p": "p.Ala319Val",
"transcript": "ENST00000930046.1",
"protein_id": "ENSP00000600105.1",
"transcript_support_level": null,
"aa_start": 319,
"aa_end": null,
"aa_length": 399,
"cds_start": 956,
"cds_end": null,
"cds_length": 1200,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930046.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Ala295Val",
"transcript": "ENST00000960174.1",
"protein_id": "ENSP00000630233.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 375,
"cds_start": 884,
"cds_end": null,
"cds_length": 1128,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960174.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.626C>T",
"hgvs_p": "p.Ala209Val",
"transcript": "ENST00000899621.1",
"protein_id": "ENSP00000569680.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 289,
"cds_start": 626,
"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": "ENST00000899621.1"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.1061C>T",
"hgvs_p": "p.Ala354Val",
"transcript": "XM_011523086.3",
"protein_id": "XP_011521388.1",
"transcript_support_level": null,
"aa_start": 354,
"aa_end": null,
"aa_length": 434,
"cds_start": 1061,
"cds_end": null,
"cds_length": 1305,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011523086.3"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.998C>T",
"hgvs_p": "p.Ala333Val",
"transcript": "XM_011523087.3",
"protein_id": "XP_011521389.1",
"transcript_support_level": null,
"aa_start": 333,
"aa_end": null,
"aa_length": 413,
"cds_start": 998,
"cds_end": null,
"cds_length": 1242,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011523087.3"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.896C>T",
"hgvs_p": "p.Ala299Val",
"transcript": "XM_011523088.3",
"protein_id": "XP_011521390.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 379,
"cds_start": 896,
"cds_end": null,
"cds_length": 1140,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011523088.3"
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "c.608C>T",
"hgvs_p": "p.Ala203Val",
"transcript": "XM_011523089.3",
"protein_id": "XP_011521391.1",
"transcript_support_level": null,
"aa_start": 203,
"aa_end": null,
"aa_length": 283,
"cds_start": 608,
"cds_end": null,
"cds_length": 852,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011523089.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"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": "MVD",
"gene_hgnc_id": 7529,
"hgvs_c": "n.240C>T",
"hgvs_p": null,
"transcript": "ENST00000561895.1",
"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": "ENST00000561895.1"
}
],
"gene_symbol": "MVD",
"gene_hgnc_id": 7529,
"dbsnp": "rs1488556161",
"frequency_reference_population": 6.8906115e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.89061e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.2389415204524994,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.036,
"revel_prediction": "Benign",
"alphamissense_score": 0.1228,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.51,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.352,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_002461.3",
"gene_symbol": "MVD",
"hgnc_id": 7529,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.959C>T",
"hgvs_p": "p.Ala320Val"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}