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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: 6-52503253-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=52503253&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 52503253,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_012288.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1057G>A",
"hgvs_p": "p.Val353Met",
"transcript": "NM_012288.4",
"protein_id": "NP_036420.1",
"transcript_support_level": null,
"aa_start": 353,
"aa_end": null,
"aa_length": 370,
"cds_start": 1057,
"cds_end": null,
"cds_length": 1113,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000182527.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012288.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1057G>A",
"hgvs_p": "p.Val353Met",
"transcript": "ENST00000182527.4",
"protein_id": "ENSP00000182527.3",
"transcript_support_level": 1,
"aa_start": 353,
"aa_end": null,
"aa_length": 370,
"cds_start": 1057,
"cds_end": null,
"cds_length": 1113,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_012288.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000182527.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1156G>A",
"hgvs_p": "p.Val386Met",
"transcript": "ENST00000956692.1",
"protein_id": "ENSP00000626751.1",
"transcript_support_level": null,
"aa_start": 386,
"aa_end": null,
"aa_length": 403,
"cds_start": 1156,
"cds_end": null,
"cds_length": 1212,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956692.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1060G>A",
"hgvs_p": "p.Val354Met",
"transcript": "ENST00000956690.1",
"protein_id": "ENSP00000626749.1",
"transcript_support_level": null,
"aa_start": 354,
"aa_end": null,
"aa_length": 371,
"cds_start": 1060,
"cds_end": null,
"cds_length": 1116,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956690.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1054G>A",
"hgvs_p": "p.Val352Met",
"transcript": "ENST00000912004.1",
"protein_id": "ENSP00000582063.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 369,
"cds_start": 1054,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912004.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1048G>A",
"hgvs_p": "p.Val350Met",
"transcript": "ENST00000863425.1",
"protein_id": "ENSP00000533484.1",
"transcript_support_level": null,
"aa_start": 350,
"aa_end": null,
"aa_length": 367,
"cds_start": 1048,
"cds_end": null,
"cds_length": 1104,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863425.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.1024G>A",
"hgvs_p": "p.Val342Met",
"transcript": "ENST00000863427.1",
"protein_id": "ENSP00000533486.1",
"transcript_support_level": null,
"aa_start": 342,
"aa_end": null,
"aa_length": 359,
"cds_start": 1024,
"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": "ENST00000863427.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.952G>A",
"hgvs_p": "p.Val318Met",
"transcript": "ENST00000863426.1",
"protein_id": "ENSP00000533485.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 335,
"cds_start": 952,
"cds_end": null,
"cds_length": 1008,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863426.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.940G>A",
"hgvs_p": "p.Val314Met",
"transcript": "ENST00000956694.1",
"protein_id": "ENSP00000626753.1",
"transcript_support_level": null,
"aa_start": 314,
"aa_end": null,
"aa_length": 331,
"cds_start": 940,
"cds_end": null,
"cds_length": 996,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956694.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.823G>A",
"hgvs_p": "p.Val275Met",
"transcript": "ENST00000956695.1",
"protein_id": "ENSP00000626754.1",
"transcript_support_level": null,
"aa_start": 275,
"aa_end": null,
"aa_length": 292,
"cds_start": 823,
"cds_end": null,
"cds_length": 879,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956695.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.808G>A",
"hgvs_p": "p.Val270Met",
"transcript": "ENST00000956693.1",
"protein_id": "ENSP00000626752.1",
"transcript_support_level": null,
"aa_start": 270,
"aa_end": null,
"aa_length": 287,
"cds_start": 808,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956693.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.766G>A",
"hgvs_p": "p.Val256Met",
"transcript": "ENST00000956691.1",
"protein_id": "ENSP00000626750.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 273,
"cds_start": 766,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956691.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.652G>A",
"hgvs_p": "p.Val218Met",
"transcript": "ENST00000912005.1",
"protein_id": "ENSP00000582064.1",
"transcript_support_level": null,
"aa_start": 218,
"aa_end": null,
"aa_length": 235,
"cds_start": 652,
"cds_end": null,
"cds_length": 708,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912005.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"hgvs_c": "c.946G>A",
"hgvs_p": "p.Val316Met",
"transcript": "XM_011515005.3",
"protein_id": "XP_011513307.1",
"transcript_support_level": null,
"aa_start": 316,
"aa_end": null,
"aa_length": 333,
"cds_start": 946,
"cds_end": null,
"cds_length": 1002,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011515005.3"
},
{
"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": 11,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "EFHC1",
"gene_hgnc_id": 16406,
"hgvs_c": "c.1851+12903C>T",
"hgvs_p": null,
"transcript": "ENST00000637353.1",
"protein_id": "ENSP00000490441.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 641,
"cds_start": null,
"cds_end": null,
"cds_length": 1926,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000637353.1"
},
{
"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": 9,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "EFHC1",
"gene_hgnc_id": 16406,
"hgvs_c": "c.1516-12642C>T",
"hgvs_p": null,
"transcript": "ENST00000636343.1",
"protein_id": "ENSP00000490193.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 517,
"cds_start": null,
"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": "ENST00000636343.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "EFHC1",
"gene_hgnc_id": 16406,
"hgvs_c": "n.*1552+12903C>T",
"hgvs_p": null,
"transcript": "ENST00000637602.1",
"protein_id": "ENSP00000490074.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000637602.1"
}
],
"gene_symbol": "TRAM2",
"gene_hgnc_id": 16855,
"dbsnp": null,
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.15354812145233154,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.114,
"revel_prediction": "Benign",
"alphamissense_score": 0.104,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.2,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.488,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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_012288.4",
"gene_symbol": "TRAM2",
"hgnc_id": 16855,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1057G>A",
"hgvs_p": "p.Val353Met"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000637602.1",
"gene_symbol": "EFHC1",
"hgnc_id": 16406,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "n.*1552+12903C>T",
"hgvs_p": null
}
],
"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
}