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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: 21-25601389-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=25601389&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "21",
"pos": 25601389,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_080794.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "NM_017446.4",
"protein_id": "NP_059142.3",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 338,
"cds_start": 499,
"cds_end": null,
"cds_length": 1017,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000352957.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017446.4"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000352957.9",
"protein_id": "ENSP00000284967.7",
"transcript_support_level": 1,
"aa_start": 167,
"aa_end": null,
"aa_length": 338,
"cds_start": 499,
"cds_end": null,
"cds_length": 1017,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_017446.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000352957.9"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "NM_080794.4",
"protein_id": "NP_542984.3",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 353,
"cds_start": 499,
"cds_end": null,
"cds_length": 1062,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_080794.4"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000307301.11",
"protein_id": "ENSP00000305682.7",
"transcript_support_level": 5,
"aa_start": 167,
"aa_end": null,
"aa_length": 353,
"cds_start": 499,
"cds_end": null,
"cds_length": 1062,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000307301.11"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.517G>A",
"hgvs_p": "p.Val173Ile",
"transcript": "ENST00000925346.1",
"protein_id": "ENSP00000595405.1",
"transcript_support_level": null,
"aa_start": 173,
"aa_end": null,
"aa_length": 344,
"cds_start": 517,
"cds_end": null,
"cds_length": 1035,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925346.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000925341.1",
"protein_id": "ENSP00000595400.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 339,
"cds_start": 499,
"cds_end": null,
"cds_length": 1020,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925341.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000946900.1",
"protein_id": "ENSP00000616959.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 337,
"cds_start": 499,
"cds_end": null,
"cds_length": 1014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946900.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.490G>A",
"hgvs_p": "p.Val164Ile",
"transcript": "ENST00000925344.1",
"protein_id": "ENSP00000595403.1",
"transcript_support_level": null,
"aa_start": 164,
"aa_end": null,
"aa_length": 325,
"cds_start": 490,
"cds_end": null,
"cds_length": 978,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925344.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000946901.1",
"protein_id": "ENSP00000616960.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 323,
"cds_start": 499,
"cds_end": null,
"cds_length": 972,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946901.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000925340.1",
"protein_id": "ENSP00000595399.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 322,
"cds_start": 499,
"cds_end": null,
"cds_length": 969,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925340.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000875588.1",
"protein_id": "ENSP00000545647.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 321,
"cds_start": 499,
"cds_end": null,
"cds_length": 966,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000875588.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.445G>A",
"hgvs_p": "p.Val149Ile",
"transcript": "ENST00000875589.1",
"protein_id": "ENSP00000545648.1",
"transcript_support_level": null,
"aa_start": 149,
"aa_end": null,
"aa_length": 320,
"cds_start": 445,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000875589.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.385G>A",
"hgvs_p": "p.Val129Ile",
"transcript": "ENST00000925343.1",
"protein_id": "ENSP00000595402.1",
"transcript_support_level": null,
"aa_start": 129,
"aa_end": null,
"aa_length": 300,
"cds_start": 385,
"cds_end": null,
"cds_length": 903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925343.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "ENST00000419219.1",
"protein_id": "ENSP00000404426.1",
"transcript_support_level": 5,
"aa_start": 167,
"aa_end": null,
"aa_length": 296,
"cds_start": 499,
"cds_end": null,
"cds_length": 891,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000419219.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.292G>A",
"hgvs_p": "p.Val98Ile",
"transcript": "ENST00000925345.1",
"protein_id": "ENSP00000595404.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 269,
"cds_start": 292,
"cds_end": null,
"cds_length": 810,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925345.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile",
"transcript": "XM_006724026.5",
"protein_id": "XP_006724089.1",
"transcript_support_level": null,
"aa_start": 167,
"aa_end": null,
"aa_length": 353,
"cds_start": 499,
"cds_end": null,
"cds_length": 1062,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006724026.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.373G>A",
"hgvs_p": "p.Val125Ile",
"transcript": "XM_011529651.3",
"protein_id": "XP_011527953.1",
"transcript_support_level": null,
"aa_start": 125,
"aa_end": null,
"aa_length": 296,
"cds_start": 373,
"cds_end": null,
"cds_length": 891,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011529651.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"hgvs_c": "c.281-1523G>A",
"hgvs_p": null,
"transcript": "ENST00000925342.1",
"protein_id": "ENSP00000595401.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 258,
"cds_start": null,
"cds_end": null,
"cds_length": 777,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925342.1"
}
],
"gene_symbol": "MRPL39",
"gene_hgnc_id": 14027,
"dbsnp": "rs373638144",
"frequency_reference_population": 0.000016765542,
"hom_count_reference_population": 0,
"allele_count_reference_population": 27,
"gnomad_exomes_af": 0.0000178277,
"gnomad_genomes_af": 0.00000657704,
"gnomad_exomes_ac": 26,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.08674946427345276,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.033,
"revel_prediction": "Benign",
"alphamissense_score": 0.0769,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.65,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.533,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 2,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_080794.4",
"gene_symbol": "MRPL39",
"hgnc_id": 14027,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.499G>A",
"hgvs_p": "p.Val167Ile"
}
],
"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
}