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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: 17-58983877-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=58983877&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 58983877,
"ref": "G",
"alt": "A",
"effect": "3_prime_UTR_variant",
"transcript": "ENST00000308249.4",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPM1E",
"gene_hgnc_id": 19322,
"hgvs_c": "c.*2846G>A",
"hgvs_p": null,
"transcript": "NM_014906.5",
"protein_id": "NP_055721.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 755,
"cds_start": -4,
"cds_end": null,
"cds_length": 2268,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6560,
"mane_select": "ENST00000308249.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPM1E",
"gene_hgnc_id": 19322,
"hgvs_c": "c.*2846G>A",
"hgvs_p": null,
"transcript": "ENST00000308249.4",
"protein_id": "ENSP00000312411.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 755,
"cds_start": -4,
"cds_end": null,
"cds_length": 2268,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6560,
"mane_select": "NM_014906.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2892-956C>T",
"hgvs_p": null,
"transcript": "ENST00000393066.7",
"protein_id": "ENSP00000376785.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 964,
"cds_start": -4,
"cds_end": null,
"cds_length": 2895,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3622,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPM1E",
"gene_hgnc_id": 19322,
"hgvs_c": "n.5043G>A",
"hgvs_p": null,
"transcript": "NR_048561.1",
"protein_id": null,
"transcript_support_level": null,
"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": 6345,
"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": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPM1E",
"gene_hgnc_id": 19322,
"hgvs_c": "c.*2846G>A",
"hgvs_p": null,
"transcript": "XM_047435630.1",
"protein_id": "XP_047291586.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 518,
"cds_start": -4,
"cds_end": null,
"cds_length": 1557,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6666,
"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": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPM1E",
"gene_hgnc_id": 19322,
"hgvs_c": "c.*2846G>A",
"hgvs_p": null,
"transcript": "XM_024450657.2",
"protein_id": "XP_024306425.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 516,
"cds_start": -4,
"cds_end": null,
"cds_length": 1551,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6865,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2892-956C>T",
"hgvs_p": null,
"transcript": "NM_001005207.5",
"protein_id": "NP_001005207.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 964,
"cds_start": -4,
"cds_end": null,
"cds_length": 2895,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": 23,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2775-956C>T",
"hgvs_p": null,
"transcript": "NM_001320989.3",
"protein_id": "NP_001307918.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 925,
"cds_start": -4,
"cds_end": null,
"cds_length": 2778,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.351-956C>T",
"hgvs_p": null,
"transcript": "ENST00000585287.5",
"protein_id": "ENSP00000464666.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 117,
"cds_start": -4,
"cds_end": null,
"cds_length": 354,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 634,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.159-956C>T",
"hgvs_p": null,
"transcript": "ENST00000583945.5",
"protein_id": "ENSP00000462778.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 53,
"cds_start": -4,
"cds_end": null,
"cds_length": 162,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 430,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2919-13778C>T",
"hgvs_p": null,
"transcript": "XM_017024662.2",
"protein_id": "XP_016880151.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 995,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 24,
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2892-13778C>T",
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"transcript": "XM_017024663.3",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 24,
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"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2919-956C>T",
"hgvs_p": null,
"transcript": "XM_005257385.2",
"protein_id": "XP_005257442.1",
"transcript_support_level": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 24,
"intron_rank": 23,
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2817-13778C>T",
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"transcript": "XM_047436107.1",
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},
{
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"consequences": [
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],
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"gene_symbol": "TRIM37",
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"transcript": "XM_047436108.1",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 23,
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2790-13778C>T",
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"transcript": "XM_047436110.1",
"protein_id": "XP_047292066.1",
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},
{
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],
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2841-956C>T",
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"transcript": "XM_017024667.2",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 24,
"intron_rank": 23,
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2775-13778C>T",
"hgvs_p": null,
"transcript": "XM_047436111.1",
"protein_id": "XP_047292067.1",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "TRIM37",
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"hgvs_c": "c.2817-956C>T",
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"transcript": "XM_047436113.1",
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},
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],
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"gene_symbol": "TRIM37",
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},
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],
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 23,
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"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2763-956C>T",
"hgvs_p": null,
"transcript": "XM_047436116.1",
"protein_id": "XP_047292072.1",
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"cds_start": -4,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 23,
"intron_rank": 22,
"intron_rank_end": null,
"gene_symbol": "TRIM37",
"gene_hgnc_id": 7523,
"hgvs_c": "c.2724-956C>T",
"hgvs_p": null,
"transcript": "XM_047436117.1",
"protein_id": "XP_047292073.1",
"transcript_support_level": null,
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{
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{
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}
],
"message": null
}