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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: 14-31066217-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=31066217&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "AP4S1",
"hgnc_id": 575,
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"inheritance_mode": "AR",
"pathogenic_score": 2,
"score": 2,
"transcript": "NM_007077.5",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_score": 2,
"allele_count_reference_population": 1,
"alphamissense_prediction": null,
"alphamissense_score": 0.6907,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.21,
"chr": "14",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "not specified",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.3226041793823242,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4060,
"cdna_start": 231,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001128126.3",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000542754.7",
"protein_coding": true,
"protein_id": "NP_001121598.1",
"strand": true,
"transcript": "NM_001128126.3",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 4060,
"cdna_start": 231,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000542754.7",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001128126.3",
"protein_coding": true,
"protein_id": "ENSP00000438170.2",
"strand": true,
"transcript": "ENST00000542754.7",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 149,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1122,
"cdna_start": 212,
"cds_end": null,
"cds_length": 450,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000334725.8",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000334484.4",
"strand": true,
"transcript": "ENST00000334725.8",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 132,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2034,
"cdna_start": 92,
"cds_end": null,
"cds_length": 399,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000216366.9",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000216366.5",
"strand": true,
"transcript": "ENST00000216366.9",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 173,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1502,
"cdna_start": 118,
"cds_end": null,
"cds_length": 522,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000313566.11",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000322508.8",
"strand": true,
"transcript": "ENST00000313566.11",
"transcript_support_level": 3
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 159,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1610,
"cdna_start": 231,
"cds_end": null,
"cds_length": 480,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_007077.5",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_009008.2",
"strand": true,
"transcript": "NM_007077.5",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 159,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1608,
"cdna_start": 229,
"cds_end": null,
"cds_length": 480,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000554345.6",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000450768.2",
"strand": true,
"transcript": "ENST00000554345.6",
"transcript_support_level": 3
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 149,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1732,
"cdna_start": 231,
"cds_end": null,
"cds_length": 450,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001254727.2",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001241656.1",
"strand": true,
"transcript": "NM_001254727.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4596,
"cdna_start": 767,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001254728.2",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001241657.1",
"strand": true,
"transcript": "NM_001254728.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4114,
"cdna_start": 285,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001254729.2",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001241658.1",
"strand": true,
"transcript": "NM_001254729.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1263,
"cdna_start": 767,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000555417.6",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000451609.2",
"strand": true,
"transcript": "ENST00000555417.6",
"transcript_support_level": 3
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1257,
"cdna_start": 446,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000556232.8",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000451918.3",
"strand": true,
"transcript": "ENST00000556232.8",
"transcript_support_level": 4
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 699,
"cdna_start": 285,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000557346.6",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000451479.2",
"strand": true,
"transcript": "ENST00000557346.6",
"transcript_support_level": 3
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1022,
"cdna_start": 214,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000713810.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000519116.1",
"strand": true,
"transcript": "ENST00000713810.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1079,
"cdna_start": 272,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000964657.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000634716.1",
"strand": true,
"transcript": "ENST00000964657.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 144,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1105,
"cdna_start": 300,
"cds_end": null,
"cds_length": 435,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000964659.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000634718.1",
"strand": true,
"transcript": "ENST00000964659.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 135,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1538,
"cdna_start": 231,
"cds_end": null,
"cds_length": 408,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001254726.2",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001241655.1",
"strand": true,
"transcript": "NM_001254726.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 135,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 889,
"cdna_start": 197,
"cds_end": null,
"cds_length": 408,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000554609.6",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000452383.2",
"strand": true,
"transcript": "ENST00000554609.6",
"transcript_support_level": 5
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 135,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2562,
"cdna_start": 242,
"cds_end": null,
"cds_length": 408,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000673317.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000500890.1",
"strand": true,
"transcript": "ENST00000673317.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 130,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1316,
"cdna_start": 413,
"cds_end": null,
"cds_length": 393,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000713808.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000519114.1",
"strand": true,
"transcript": "ENST00000713808.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 121,
"aa_ref": "M",
"aa_start": 7,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1139,
"cdna_start": 414,
"cds_end": null,
"cds_length": 366,
"cds_start": 21,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000964658.1",
"gene_hgnc_id": 575,
"gene_symbol": "AP4S1",
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Met7Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000634717.1",
"strand": true,
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