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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: 12-122137490-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=122137490&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 122137490,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_014938.6",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "NM_014938.6",
"protein_id": "NP_055753.3",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 919,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2760,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000319080.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014938.6"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "ENST00000319080.12",
"protein_id": "ENSP00000312834.6",
"transcript_support_level": 1,
"aa_start": 685,
"aa_end": null,
"aa_length": 919,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2760,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014938.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000319080.12"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.875G>C",
"hgvs_p": "p.Gly292Ala",
"transcript": "ENST00000538698.5",
"protein_id": "ENSP00000440769.1",
"transcript_support_level": 1,
"aa_start": 292,
"aa_end": null,
"aa_length": 526,
"cds_start": 875,
"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": "ENST00000538698.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "ENST00000890512.1",
"protein_id": "ENSP00000560571.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 920,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2763,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890512.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2042G>C",
"hgvs_p": "p.Gly681Ala",
"transcript": "ENST00000890511.1",
"protein_id": "ENSP00000560570.1",
"transcript_support_level": null,
"aa_start": 681,
"aa_end": null,
"aa_length": 915,
"cds_start": 2042,
"cds_end": null,
"cds_length": 2748,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890511.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1322G>C",
"hgvs_p": "p.Gly441Ala",
"transcript": "ENST00000945226.1",
"protein_id": "ENSP00000615285.1",
"transcript_support_level": null,
"aa_start": 441,
"aa_end": null,
"aa_length": 676,
"cds_start": 1322,
"cds_end": null,
"cds_length": 2031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945226.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1322G>C",
"hgvs_p": "p.Gly441Ala",
"transcript": "ENST00000945227.1",
"protein_id": "ENSP00000615286.1",
"transcript_support_level": null,
"aa_start": 441,
"aa_end": null,
"aa_length": 675,
"cds_start": 1322,
"cds_end": null,
"cds_length": 2028,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945227.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1322G>C",
"hgvs_p": "p.Gly441Ala",
"transcript": "ENST00000945229.1",
"protein_id": "ENSP00000615288.1",
"transcript_support_level": null,
"aa_start": 441,
"aa_end": null,
"aa_length": 658,
"cds_start": 1322,
"cds_end": null,
"cds_length": 1977,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945229.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1022G>C",
"hgvs_p": "p.Gly341Ala",
"transcript": "ENST00000945225.1",
"protein_id": "ENSP00000615284.1",
"transcript_support_level": null,
"aa_start": 341,
"aa_end": null,
"aa_length": 576,
"cds_start": 1022,
"cds_end": null,
"cds_length": 1731,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945225.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1022G>C",
"hgvs_p": "p.Gly341Ala",
"transcript": "ENST00000945228.1",
"protein_id": "ENSP00000615287.1",
"transcript_support_level": null,
"aa_start": 341,
"aa_end": null,
"aa_length": 575,
"cds_start": 1022,
"cds_end": null,
"cds_length": 1728,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945228.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.467G>C",
"hgvs_p": "p.Gly156Ala",
"transcript": "ENST00000366272.6",
"protein_id": "ENSP00000445891.1",
"transcript_support_level": 3,
"aa_start": 156,
"aa_end": null,
"aa_length": 307,
"cds_start": 467,
"cds_end": null,
"cds_length": 924,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000366272.6"
},
{
"aa_ref": "G",
"aa_alt": "A",
"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": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.59G>C",
"hgvs_p": "p.Gly20Ala",
"transcript": "ENST00000542417.1",
"protein_id": "ENSP00000444507.1",
"transcript_support_level": 2,
"aa_start": 20,
"aa_end": null,
"aa_length": 169,
"cds_start": 59,
"cds_end": null,
"cds_length": 511,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000542417.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "XM_006719290.5",
"protein_id": "XP_006719353.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 960,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2883,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719290.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "XM_006719291.5",
"protein_id": "XP_006719354.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 959,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2880,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719291.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "XM_006719292.5",
"protein_id": "XP_006719355.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 920,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2763,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719292.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala",
"transcript": "XM_047428537.1",
"protein_id": "XP_047284493.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 771,
"cds_start": 2054,
"cds_end": null,
"cds_length": 2316,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047428537.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.1178+1824G>C",
"hgvs_p": null,
"transcript": "ENST00000945230.1",
"protein_id": "ENSP00000615289.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 518,
"cds_start": null,
"cds_end": null,
"cds_length": 1557,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000945230.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.2033-704G>C",
"hgvs_p": null,
"transcript": "XM_047428538.1",
"protein_id": "XP_047284494.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 686,
"cds_start": null,
"cds_end": null,
"cds_length": 2061,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047428538.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "n.2441G>C",
"hgvs_p": null,
"transcript": "ENST00000541750.1",
"protein_id": null,
"transcript_support_level": 5,
"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": "ENST00000541750.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"hgvs_c": "c.*102G>C",
"hgvs_p": null,
"transcript": "XM_006719293.4",
"protein_id": "XP_006719356.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 708,
"cds_start": null,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719293.4"
}
],
"gene_symbol": "MLXIP",
"gene_hgnc_id": 17055,
"dbsnp": "rs1345556667",
"frequency_reference_population": 6.841761e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84176e-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": 0.23851856589317322,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.103,
"revel_prediction": "Benign",
"alphamissense_score": 0.1419,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.37,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.157,
"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": 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_014938.6",
"gene_symbol": "MLXIP",
"hgnc_id": 17055,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2054G>C",
"hgvs_p": "p.Gly685Ala"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}