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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: 8-144474259-CAG-TAA (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=144474259&ref=CAG&alt=TAA&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 1,
"criteria": [
"BP7"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "FOXH1",
"hgnc_id": 3814,
"hgvs_c": "c.1075_1077delCTGinsTTA",
"hgvs_p": "p.360",
"inheritance_mode": "Unknown",
"pathogenic_score": 0,
"score": -1,
"transcript": "NM_003923.3",
"verdict": "Likely_benign"
},
{
"benign_score": 0,
"criteria": [],
"effects": [
"downstream_gene_variant"
],
"gene_symbol": "KIFC2",
"hgnc_id": 29530,
"hgvs_c": "c.*809_*811delCAGinsTAA",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 0,
"score": 0,
"transcript": "NM_145754.5",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP7",
"acmg_score": -1,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "TAA",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "8",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 365,
"aa_ref": "L",
"aa_start": 359,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2017,
"cdna_start": 1170,
"cds_end": null,
"cds_length": 1098,
"cds_start": 1075,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_003923.3",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.1075_1077delCTGinsTTA",
"hgvs_p": "p.360",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000377317.5",
"protein_coding": true,
"protein_id": "NP_003914.1",
"strand": false,
"transcript": "NM_003923.3",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 365,
"aa_ref": "L",
"aa_start": 359,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2017,
"cdna_start": 1170,
"cds_end": null,
"cds_length": 1098,
"cds_start": 1075,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377317.5",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.1075_1077delCTGinsTTA",
"hgvs_p": "p.360",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_003923.3",
"protein_coding": true,
"protein_id": "ENSP00000366534.4",
"strand": false,
"transcript": "ENST00000377317.5",
"transcript_support_level": 1
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 362,
"aa_ref": "L",
"aa_start": 356,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1692,
"cdna_start": 1165,
"cds_end": null,
"cds_length": 1089,
"cds_start": 1066,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000935088.1",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.1066_1068delCTGinsTTA",
"hgvs_p": "p.357",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605147.1",
"strand": false,
"transcript": "ENST00000935088.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 361,
"aa_ref": "L",
"aa_start": 355,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1684,
"cdna_start": 1157,
"cds_end": null,
"cds_length": 1086,
"cds_start": 1063,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000935090.1",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.1063_1065delCTGinsTTA",
"hgvs_p": "p.356",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605149.1",
"strand": false,
"transcript": "ENST00000935090.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 359,
"aa_ref": "L",
"aa_start": 353,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1700,
"cdna_start": 1173,
"cds_end": null,
"cds_length": 1080,
"cds_start": 1057,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000935087.1",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.1057_1059delCTGinsTTA",
"hgvs_p": "p.354",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605146.1",
"strand": false,
"transcript": "ENST00000935087.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 330,
"aa_ref": "L",
"aa_start": 324,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1595,
"cdna_start": 1068,
"cds_end": null,
"cds_length": 993,
"cds_start": 970,
"consequences": [
"synonymous_variant"
],
"exon_count": 2,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000935089.1",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.970_972delCTGinsTTA",
"hgvs_p": "p.325",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605148.1",
"strand": false,
"transcript": "ENST00000935089.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 321,
"aa_ref": "L",
"aa_start": 315,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1589,
"cdna_start": 1062,
"cds_end": null,
"cds_length": 966,
"cds_start": 943,
"consequences": [
"synonymous_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000935086.1",
"gene_hgnc_id": 3814,
"gene_symbol": "FOXH1",
"hgvs_c": "c.943_945delCTGinsTTA",
"hgvs_p": "p.316",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000605145.1",
"strand": false,
"transcript": "ENST00000935086.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 791,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3272,
"cdna_start": null,
"cds_end": null,
"cds_length": 2376,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001369769.2",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000645548.2",
"protein_coding": true,
"protein_id": "NP_001356698.1",
"strand": true,
"transcript": "NM_001369769.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 791,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3272,
"cdna_start": null,
"cds_end": null,
"cds_length": 2376,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000645548.2",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001369769.2",
"protein_coding": true,
"protein_id": "ENSP00000494595.1",
"strand": true,
"transcript": "ENST00000645548.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 838,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3247,
"cdna_start": null,
"cds_end": null,
"cds_length": 2517,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000301332.3",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*809_*811delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000301332.2",
"strand": true,
"transcript": "ENST00000301332.3",
"transcript_support_level": 1
},
{
"aa_alt": null,
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"aa_length": 838,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3352,
"cdna_start": null,
"cds_end": null,
"cds_length": 2517,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_145754.5",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*809_*811delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_665697.1",
"strand": true,
"transcript": "NM_145754.5",
"transcript_support_level": null
},
{
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"aa_length": 821,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3279,
"cdna_start": null,
"cds_end": null,
"cds_length": 2466,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 19,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880943.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000551002.1",
"strand": true,
"transcript": "ENST00000880943.1",
"transcript_support_level": null
},
{
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"aa_ref": null,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3221,
"cdna_start": null,
"cds_end": null,
"cds_length": 2439,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 17,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880945.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000551004.1",
"strand": true,
"transcript": "ENST00000880945.1",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 804,
"aa_ref": null,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3195,
"cdna_start": null,
"cds_end": null,
"cds_length": 2415,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 19,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000966083.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000636142.1",
"strand": true,
"transcript": "ENST00000966083.1",
"transcript_support_level": null
},
{
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"aa_length": 775,
"aa_ref": null,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3142,
"cdna_start": null,
"cds_end": null,
"cds_length": 2328,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880942.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000551001.1",
"strand": true,
"transcript": "ENST00000880942.1",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 773,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3133,
"cdna_start": null,
"cds_end": null,
"cds_length": 2322,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880944.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000551003.1",
"strand": true,
"transcript": "ENST00000880944.1",
"transcript_support_level": null
},
{
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"aa_end": null,
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"aa_ref": null,
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2978,
"cdna_start": null,
"cds_end": null,
"cds_length": 2151,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 16,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880941.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000551000.1",
"strand": true,
"transcript": "ENST00000880941.1",
"transcript_support_level": null
},
{
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3015,
"cdna_start": null,
"cds_end": null,
"cds_length": 1809,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000880940.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*870_*872delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
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"mane_plus": null,
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"protein_coding": true,
"protein_id": "ENSP00000550999.1",
"strand": true,
"transcript": "ENST00000880940.1",
"transcript_support_level": null
},
{
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"biotype": "protein_coding",
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"cdna_end": null,
"cdna_length": 3282,
"cdna_start": null,
"cds_end": null,
"cds_length": 1761,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047422405.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*809_*811delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278361.1",
"strand": true,
"transcript": "XM_047422405.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 586,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3416,
"cdna_start": null,
"cds_end": null,
"cds_length": 1761,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 18,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047422406.1",
"gene_hgnc_id": 29530,
"gene_symbol": "KIFC2",
"hgvs_c": "c.*809_*811delCAGinsTAA",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047278362.1",
"strand": true,
"transcript": "XM_047422406.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 3646,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
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