← 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: X-43767585-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=43767585&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 43767585,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_000898.5",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1444T>A",
"hgvs_p": "p.Leu482Met",
"transcript": "NM_000898.5",
"protein_id": "NP_000889.3",
"transcript_support_level": null,
"aa_start": 482,
"aa_end": null,
"aa_length": 520,
"cds_start": 1444,
"cds_end": null,
"cds_length": 1563,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000378069.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000898.5"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1444T>A",
"hgvs_p": "p.Leu482Met",
"transcript": "ENST00000378069.5",
"protein_id": "ENSP00000367309.4",
"transcript_support_level": 1,
"aa_start": 482,
"aa_end": null,
"aa_length": 520,
"cds_start": 1444,
"cds_end": null,
"cds_length": 1563,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000898.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000378069.5"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1549T>A",
"hgvs_p": "p.Leu517Met",
"transcript": "ENST00000890313.1",
"protein_id": "ENSP00000560372.1",
"transcript_support_level": null,
"aa_start": 517,
"aa_end": null,
"aa_length": 555,
"cds_start": 1549,
"cds_end": null,
"cds_length": 1668,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890313.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1462T>A",
"hgvs_p": "p.Leu488Met",
"transcript": "ENST00000890309.1",
"protein_id": "ENSP00000560368.1",
"transcript_support_level": null,
"aa_start": 488,
"aa_end": null,
"aa_length": 526,
"cds_start": 1462,
"cds_end": null,
"cds_length": 1581,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890309.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1441T>A",
"hgvs_p": "p.Leu481Met",
"transcript": "ENST00000890307.1",
"protein_id": "ENSP00000560366.1",
"transcript_support_level": null,
"aa_start": 481,
"aa_end": null,
"aa_length": 519,
"cds_start": 1441,
"cds_end": null,
"cds_length": 1560,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890307.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1441T>A",
"hgvs_p": "p.Leu481Met",
"transcript": "ENST00000890310.1",
"protein_id": "ENSP00000560369.1",
"transcript_support_level": null,
"aa_start": 481,
"aa_end": null,
"aa_length": 519,
"cds_start": 1441,
"cds_end": null,
"cds_length": 1560,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890310.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1435T>A",
"hgvs_p": "p.Leu479Met",
"transcript": "ENST00000890312.1",
"protein_id": "ENSP00000560371.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 517,
"cds_start": 1435,
"cds_end": null,
"cds_length": 1554,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890312.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1411T>A",
"hgvs_p": "p.Leu471Met",
"transcript": "ENST00000962443.1",
"protein_id": "ENSP00000632502.1",
"transcript_support_level": null,
"aa_start": 471,
"aa_end": null,
"aa_length": 509,
"cds_start": 1411,
"cds_end": null,
"cds_length": 1530,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000962443.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1378T>A",
"hgvs_p": "p.Leu460Met",
"transcript": "ENST00000962442.1",
"protein_id": "ENSP00000632501.1",
"transcript_support_level": null,
"aa_start": 460,
"aa_end": null,
"aa_length": 498,
"cds_start": 1378,
"cds_end": null,
"cds_length": 1497,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000962442.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1339T>A",
"hgvs_p": "p.Leu447Met",
"transcript": "ENST00000890308.1",
"protein_id": "ENSP00000560367.1",
"transcript_support_level": null,
"aa_start": 447,
"aa_end": null,
"aa_length": 485,
"cds_start": 1339,
"cds_end": null,
"cds_length": 1458,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890308.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1324T>A",
"hgvs_p": "p.Leu442Met",
"transcript": "ENST00000962441.1",
"protein_id": "ENSP00000632500.1",
"transcript_support_level": null,
"aa_start": 442,
"aa_end": null,
"aa_length": 480,
"cds_start": 1324,
"cds_end": null,
"cds_length": 1443,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000962441.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1306T>A",
"hgvs_p": "p.Leu436Met",
"transcript": "ENST00000890306.1",
"protein_id": "ENSP00000560365.1",
"transcript_support_level": null,
"aa_start": 436,
"aa_end": null,
"aa_length": 474,
"cds_start": 1306,
"cds_end": null,
"cds_length": 1425,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890306.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1234T>A",
"hgvs_p": "p.Leu412Met",
"transcript": "ENST00000890311.1",
"protein_id": "ENSP00000560370.1",
"transcript_support_level": null,
"aa_start": 412,
"aa_end": null,
"aa_length": 450,
"cds_start": 1234,
"cds_end": null,
"cds_length": 1353,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890311.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1201T>A",
"hgvs_p": "p.Leu401Met",
"transcript": "ENST00000962440.1",
"protein_id": "ENSP00000632499.1",
"transcript_support_level": null,
"aa_start": 401,
"aa_end": null,
"aa_length": 439,
"cds_start": 1201,
"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": "ENST00000962440.1"
},
{
"aa_ref": "L",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"hgvs_c": "c.1396T>A",
"hgvs_p": "p.Leu466Met",
"transcript": "XM_017029524.3",
"protein_id": "XP_016885013.1",
"transcript_support_level": null,
"aa_start": 466,
"aa_end": null,
"aa_length": 504,
"cds_start": 1396,
"cds_end": null,
"cds_length": 1515,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029524.3"
}
],
"gene_symbol": "MAOB",
"gene_hgnc_id": 6834,
"dbsnp": "rs149656736",
"frequency_reference_population": 0.00019020903,
"hom_count_reference_population": 61,
"allele_count_reference_population": 230,
"gnomad_exomes_af": 0.0000920497,
"gnomad_genomes_af": 0.00115217,
"gnomad_exomes_ac": 101,
"gnomad_genomes_ac": 129,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.008376777172088623,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.06,
"revel_prediction": "Benign",
"alphamissense_score": 0.1258,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.74,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.711,
"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": -10,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Moderate,BS2",
"acmg_by_gene": [
{
"score": -10,
"benign_score": 10,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_000898.5",
"gene_symbol": "MAOB",
"hgnc_id": 6834,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.1444T>A",
"hgvs_p": "p.Leu482Met"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}