← 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: 19-46722920-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=46722920&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 46722920,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000263280.11",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1796C>A",
"hgvs_p": "p.Thr599Asn",
"transcript": "NM_013403.3",
"protein_id": "NP_037535.2",
"transcript_support_level": null,
"aa_start": 599,
"aa_end": null,
"aa_length": 753,
"cds_start": 1796,
"cds_end": null,
"cds_length": 2262,
"cdna_start": 1816,
"cdna_end": null,
"cdna_length": 3176,
"mane_select": "ENST00000263280.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1796C>A",
"hgvs_p": "p.Thr599Asn",
"transcript": "ENST00000263280.11",
"protein_id": "ENSP00000263280.4",
"transcript_support_level": 1,
"aa_start": 599,
"aa_end": null,
"aa_length": 753,
"cds_start": 1796,
"cds_end": null,
"cds_length": 2262,
"cdna_start": 1816,
"cdna_end": null,
"cdna_length": 3176,
"mane_select": "NM_013403.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1817C>A",
"hgvs_p": "p.Thr606Asn",
"transcript": "NM_001039877.2",
"protein_id": "NP_001034966.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 760,
"cds_start": 1817,
"cds_end": null,
"cds_length": 2283,
"cdna_start": 1837,
"cdna_end": null,
"cdna_length": 3197,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1817C>A",
"hgvs_p": "p.Thr606Asn",
"transcript": "ENST00000391910.7",
"protein_id": "ENSP00000375777.1",
"transcript_support_level": 5,
"aa_start": 606,
"aa_end": null,
"aa_length": 760,
"cds_start": 1817,
"cds_end": null,
"cds_length": 2283,
"cdna_start": 2268,
"cdna_end": null,
"cdna_length": 3628,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1439C>A",
"hgvs_p": "p.Thr480Asn",
"transcript": "ENST00000539396.5",
"protein_id": "ENSP00000440901.1",
"transcript_support_level": 2,
"aa_start": 480,
"aa_end": null,
"aa_length": 634,
"cds_start": 1439,
"cds_end": null,
"cds_length": 1905,
"cdna_start": 1808,
"cdna_end": null,
"cdna_length": 2608,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.836C>A",
"hgvs_p": "p.Thr279Asn",
"transcript": "ENST00000594287.6",
"protein_id": "ENSP00000470634.2",
"transcript_support_level": 5,
"aa_start": 279,
"aa_end": null,
"aa_length": 315,
"cds_start": 836,
"cds_end": null,
"cds_length": 949,
"cdna_start": 838,
"cdna_end": null,
"cdna_length": 951,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.128C>A",
"hgvs_p": "p.Thr43Asn",
"transcript": "ENST00000600615.5",
"protein_id": "ENSP00000472938.1",
"transcript_support_level": 2,
"aa_start": 43,
"aa_end": null,
"aa_length": 197,
"cds_start": 128,
"cds_end": null,
"cds_length": 594,
"cdna_start": 129,
"cdna_end": null,
"cdna_length": 788,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1862C>A",
"hgvs_p": "p.Thr621Asn",
"transcript": "XM_006723171.3",
"protein_id": "XP_006723234.1",
"transcript_support_level": null,
"aa_start": 621,
"aa_end": null,
"aa_length": 775,
"cds_start": 1862,
"cds_end": null,
"cds_length": 2328,
"cdna_start": 1882,
"cdna_end": null,
"cdna_length": 3242,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1841C>A",
"hgvs_p": "p.Thr614Asn",
"transcript": "XM_006723172.3",
"protein_id": "XP_006723235.1",
"transcript_support_level": null,
"aa_start": 614,
"aa_end": null,
"aa_length": 768,
"cds_start": 1841,
"cds_end": null,
"cds_length": 2307,
"cdna_start": 1861,
"cdna_end": null,
"cdna_length": 3221,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1505C>A",
"hgvs_p": "p.Thr502Asn",
"transcript": "XM_047438712.1",
"protein_id": "XP_047294668.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 656,
"cds_start": 1505,
"cds_end": null,
"cds_length": 1971,
"cdna_start": 1959,
"cdna_end": null,
"cdna_length": 3319,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1460C>A",
"hgvs_p": "p.Thr487Asn",
"transcript": "XM_047438713.1",
"protein_id": "XP_047294669.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 641,
"cds_start": 1460,
"cds_end": null,
"cds_length": 1926,
"cdna_start": 1914,
"cdna_end": null,
"cdna_length": 3274,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1439C>A",
"hgvs_p": "p.Thr480Asn",
"transcript": "XM_047438714.1",
"protein_id": "XP_047294670.1",
"transcript_support_level": null,
"aa_start": 480,
"aa_end": null,
"aa_length": 634,
"cds_start": 1439,
"cds_end": null,
"cds_length": 1905,
"cdna_start": 1893,
"cdna_end": null,
"cdna_length": 3253,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "c.1238C>A",
"hgvs_p": "p.Thr413Asn",
"transcript": "XM_047438715.1",
"protein_id": "XP_047294671.1",
"transcript_support_level": null,
"aa_start": 413,
"aa_end": null,
"aa_length": 567,
"cds_start": 1238,
"cds_end": null,
"cds_length": 1704,
"cdna_start": 1397,
"cdna_end": null,
"cdna_length": 2757,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "n.1165C>A",
"hgvs_p": null,
"transcript": "ENST00000594581.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2692,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "n.1064C>A",
"hgvs_p": null,
"transcript": "ENST00000595357.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1602,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "n.1065C>A",
"hgvs_p": null,
"transcript": "ENST00000601631.6",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1125,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "n.*14C>A",
"hgvs_p": null,
"transcript": "ENST00000594357.6",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 850,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"hgvs_c": "n.*3C>A",
"hgvs_p": null,
"transcript": "ENST00000598074.1",
"protein_id": null,
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 448,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "STRN4",
"gene_hgnc_id": 15721,
"dbsnp": "rs375959219",
"frequency_reference_population": 0.000013136461,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.0000131365,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.2638210356235504,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.272,
"revel_prediction": "Benign",
"alphamissense_score": 0.1731,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.29,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.008,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.02,
"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": "ENST00000263280.11",
"gene_symbol": "STRN4",
"hgnc_id": 15721,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1796C>A",
"hgvs_p": "p.Thr599Asn"
}
],
"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
}