← 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: 11-9724820-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=9724820&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 9724820,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_015055.4",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "NM_015055.4",
"protein_id": "NP_055870.2",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 585,
"cds_start": 577,
"cds_end": null,
"cds_length": 1758,
"cdna_start": 680,
"cdna_end": null,
"cdna_length": 4884,
"mane_select": "ENST00000318950.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015055.4"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000318950.11",
"protein_id": "ENSP00000315630.6",
"transcript_support_level": 1,
"aa_start": 193,
"aa_end": null,
"aa_length": 585,
"cds_start": 577,
"cds_end": null,
"cds_length": 1758,
"cdna_start": 680,
"cdna_end": null,
"cdna_length": 4884,
"mane_select": "NM_015055.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000318950.11"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "n.622C>G",
"hgvs_p": null,
"transcript": "ENST00000524817.5",
"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": 3006,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000524817.5"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000868909.1",
"protein_id": "ENSP00000538968.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 549,
"cds_start": 577,
"cds_end": null,
"cds_length": 1650,
"cdna_start": 670,
"cdna_end": null,
"cdna_length": 2250,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868909.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.436C>G",
"hgvs_p": "p.Arg146Gly",
"transcript": "ENST00000966579.1",
"protein_id": "ENSP00000636638.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 538,
"cds_start": 436,
"cds_end": null,
"cds_length": 1617,
"cdna_start": 539,
"cdna_end": null,
"cdna_length": 4700,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966579.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.403C>G",
"hgvs_p": "p.Arg135Gly",
"transcript": "NM_001297714.2",
"protein_id": "NP_001284643.1",
"transcript_support_level": null,
"aa_start": 135,
"aa_end": null,
"aa_length": 527,
"cds_start": 403,
"cds_end": null,
"cds_length": 1584,
"cdna_start": 506,
"cdna_end": null,
"cdna_length": 4710,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001297714.2"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.403C>G",
"hgvs_p": "p.Arg135Gly",
"transcript": "ENST00000447399.6",
"protein_id": "ENSP00000399056.2",
"transcript_support_level": 2,
"aa_start": 135,
"aa_end": null,
"aa_length": 527,
"cds_start": 403,
"cds_end": null,
"cds_length": 1584,
"cdna_start": 506,
"cdna_end": null,
"cdna_length": 3538,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000447399.6"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000868911.1",
"protein_id": "ENSP00000538970.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 519,
"cds_start": 577,
"cds_end": null,
"cds_length": 1560,
"cdna_start": 629,
"cdna_end": null,
"cdna_length": 2014,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868911.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.130C>G",
"hgvs_p": "p.Arg44Gly",
"transcript": "ENST00000534662.1",
"protein_id": "ENSP00000435587.1",
"transcript_support_level": 5,
"aa_start": 44,
"aa_end": null,
"aa_length": 225,
"cds_start": 130,
"cds_end": null,
"cds_length": 680,
"cdna_start": 581,
"cdna_end": null,
"cdna_length": 1131,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000534662.1"
},
{
"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": 11,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.415-3233C>G",
"hgvs_p": null,
"transcript": "ENST00000868908.1",
"protein_id": "ENSP00000538967.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 509,
"cds_start": null,
"cds_end": null,
"cds_length": 1530,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4618,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868908.1"
},
{
"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": 11,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.415-3233C>G",
"hgvs_p": null,
"transcript": "ENST00000966580.1",
"protein_id": "ENSP00000636639.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 495,
"cds_start": null,
"cds_end": null,
"cds_length": 1488,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3413,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000966580.1"
},
{
"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": 2,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "c.241-3233C>G",
"hgvs_p": null,
"transcript": "ENST00000868910.1",
"protein_id": "ENSP00000538969.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 451,
"cds_start": null,
"cds_end": null,
"cds_length": 1356,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1834,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868910.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "n.*180C>G",
"hgvs_p": null,
"transcript": "ENST00000526358.5",
"protein_id": "ENSP00000431768.1",
"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": 813,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526358.5"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "n.481C>G",
"hgvs_p": null,
"transcript": "ENST00000531814.5",
"protein_id": null,
"transcript_support_level": 3,
"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": 716,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000531814.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"hgvs_c": "n.*180C>G",
"hgvs_p": null,
"transcript": "ENST00000526358.5",
"protein_id": "ENSP00000431768.1",
"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": 813,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000526358.5"
}
],
"gene_symbol": "SWAP70",
"gene_hgnc_id": 17070,
"dbsnp": "rs560808312",
"frequency_reference_population": 6.841059e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84106e-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": 0.12459695339202881,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.088,
"revel_prediction": "Benign",
"alphamissense_score": 0.1193,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.4,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.644,
"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_015055.4",
"gene_symbol": "SWAP70",
"hgnc_id": 17070,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}