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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: 5-36608922-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=36608922&ref=T&alt=A&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "5",
"pos": 36608922,
"ref": "T",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000265113.9",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.*301T>A",
"hgvs_p": null,
"transcript": "ENST00000512374.1",
"protein_id": "ENSP00000506048.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 65,
"cds_start": -4,
"cds_end": null,
"cds_length": 198,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1096,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_004172.5",
"protein_id": "NP_004163.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3919,
"mane_select": "ENST00000265113.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "ENST00000265113.9",
"protein_id": "ENSP00000265113.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3919,
"mane_select": "NM_004172.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "ENST00000381918.4",
"protein_id": "ENSP00000371343.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3834,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.*301T>A",
"hgvs_p": null,
"transcript": "NM_001166696.3",
"protein_id": "NP_001160168.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 65,
"cds_start": -4,
"cds_end": null,
"cds_length": 198,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1101,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 2,
"intron_rank_end": null,
"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_001438458.1",
"protein_id": "NP_001425387.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 589,
"cds_start": -4,
"cds_end": null,
"cds_length": 1770,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4060,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 2,
"intron_rank_end": null,
"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "ENST00000680232.1",
"protein_id": "ENSP00000506207.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 589,
"cds_start": -4,
"cds_end": null,
"cds_length": 1770,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4194,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_001438454.1",
"protein_id": "NP_001425383.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4007,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_001438455.1",
"protein_id": "NP_001425384.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3880,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_001438456.1",
"protein_id": "NP_001425385.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 4058,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"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": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
"hgvs_p": null,
"transcript": "NM_001438457.1",
"protein_id": "NP_001425386.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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},
{
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"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"gene_symbol": "SLC1A3",
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"hgvs_c": "c.181+318T>A",
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"transcript": "ENST00000679983.1",
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"cds_start": -4,
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},
{
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"strand": true,
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"intron_variant"
],
"exon_rank": null,
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"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
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"transcript": "ENST00000679992.1",
"protein_id": "ENSP00000506585.1",
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],
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"exon_count": 10,
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"gene_symbol": "SLC1A3",
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"hgvs_c": "c.181+318T>A",
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"transcript": "ENST00000680318.1",
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},
{
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],
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"gene_symbol": "SLC1A3",
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"hgvs_c": "c.181+318T>A",
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"feature": null
},
{
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"strand": true,
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],
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"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.181+318T>A",
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"transcript": "NM_001438459.1",
"protein_id": "NP_001425388.1",
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"gene_symbol": "SLC1A3",
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"transcript": "ENST00000680125.1",
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},
{
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],
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"gene_symbol": "SLC1A3",
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"transcript": "ENST00000681926.1",
"protein_id": "ENSP00000505850.1",
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"gene_symbol": "SLC1A3",
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],
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"gene_symbol": "SLC1A3",
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],
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"gene_symbol": "SLC1A3",
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},
{
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],
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"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.-290+318T>A",
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"transcript": "NM_001438460.1",
"protein_id": "NP_001425389.1",
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"feature": null
},
{
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"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "SLC1A3",
"gene_hgnc_id": 10941,
"hgvs_c": "c.-290+318T>A",
"hgvs_p": null,
"transcript": "NM_001438461.1",
"protein_id": "NP_001425390.1",
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},
{
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{
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{
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],
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"splice_prediction_selected": "Benign",
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"acmg_by_gene": [
{
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"BP4_Strong"
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"verdict": "Likely_benign",
"transcript": "ENST00000265113.9",
"gene_symbol": "SLC1A3",
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"effects": [
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],
"inheritance_mode": "AD,Unknown",
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}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}