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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: X-31444532-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=31444532&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 10,
"criteria": [
"BP4_Strong",
"BP6",
"BP7",
"BS2"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "DMD",
"hgnc_id": 2928,
"hgvs_c": "c.9033G>A",
"hgvs_p": "p.Pro3011Pro",
"inheritance_mode": "XL,AD",
"pathogenic_score": 0,
"score": -10,
"transcript": "NM_004006.3",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BP7,BS2",
"acmg_score": -10,
"allele_count_reference_population": 144,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.29,
"chr": "X",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": "Becker muscular dystrophy,Cardiomyopathy,Cardiovascular phenotype,Dilated cardiomyopathy 3B,Duchenne muscular dystrophy,Dystrophin deficiency,not provided",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:2 LB:1 B:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.014999999664723873,
"computational_source_selected": "REVEL",
"consequences": [
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3685,
"aa_ref": "P",
"aa_start": 3011,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 13992,
"cdna_start": 9270,
"cds_end": null,
"cds_length": 11058,
"cds_start": 9033,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "NM_004006.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.9033G>A",
"hgvs_p": "p.Pro3011Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000357033.9",
"protein_coding": true,
"protein_id": "NP_003997.2",
"strand": false,
"transcript": "NM_004006.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3685,
"aa_ref": "P",
"aa_start": 3011,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 13992,
"cdna_start": 9270,
"cds_end": null,
"cds_length": 11058,
"cds_start": 9033,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "ENST00000357033.9",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.9033G>A",
"hgvs_p": "p.Pro3011Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_004006.3",
"protein_coding": true,
"protein_id": "ENSP00000354923.3",
"strand": false,
"transcript": "ENST00000357033.9",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3681,
"aa_ref": "P",
"aa_start": 3007,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 14000,
"cdna_start": 9284,
"cds_end": null,
"cds_length": 11046,
"cds_start": 9021,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "NM_004009.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.9021G>A",
"hgvs_p": "p.Pro3007Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004000.1",
"strand": false,
"transcript": "NM_004009.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3681,
"aa_ref": "P",
"aa_start": 3007,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 13932,
"cdna_start": 9216,
"cds_end": null,
"cds_length": 11046,
"cds_start": 9021,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "ENST00000378677.6",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.9021G>A",
"hgvs_p": "p.Pro3007Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000367948.2",
"strand": false,
"transcript": "ENST00000378677.6",
"transcript_support_level": 5
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3677,
"aa_ref": "P",
"aa_start": 3003,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 13854,
"cdna_start": 9132,
"cds_end": null,
"cds_length": 11034,
"cds_start": 9009,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "NM_000109.4",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.9009G>A",
"hgvs_p": "p.Pro3003Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_000100.3",
"strand": false,
"transcript": "NM_000109.4",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 3562,
"aa_ref": "P",
"aa_start": 2888,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 14083,
"cdna_start": 9367,
"cds_end": null,
"cds_length": 10689,
"cds_start": 8664,
"consequences": [
"synonymous_variant"
],
"exon_count": 79,
"exon_rank": 60,
"exon_rank_end": null,
"feature": "NM_004010.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.8664G>A",
"hgvs_p": "p.Pro2888Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004001.1",
"strand": false,
"transcript": "NM_004010.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 2344,
"aa_ref": "P",
"aa_start": 1670,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9751,
"cdna_start": 5029,
"cds_end": null,
"cds_length": 7035,
"cds_start": 5010,
"consequences": [
"synonymous_variant"
],
"exon_count": 51,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "NM_004011.4",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.5010G>A",
"hgvs_p": "p.Pro1670Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004002.3",
"strand": false,
"transcript": "NM_004011.4",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 2341,
"aa_ref": "P",
"aa_start": 1667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9894,
"cdna_start": 5172,
"cds_end": null,
"cds_length": 7026,
"cds_start": 5001,
"consequences": [
"synonymous_variant"
],
"exon_count": 51,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "NM_004012.4",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.5001G>A",
"hgvs_p": "p.Pro1667Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004003.2",
"strand": false,
"transcript": "NM_004012.4",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 2341,
"aa_ref": "P",
"aa_start": 1667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9903,
"cdna_start": 5181,
"cds_end": null,
"cds_length": 7026,
"cds_start": 5001,
"consequences": [
"synonymous_variant"
],
"exon_count": 51,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000619831.5",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.5001G>A",
"hgvs_p": "p.Pro1667Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000479270.2",
"strand": false,
"transcript": "ENST00000619831.5",
"transcript_support_level": 5
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1972,
"aa_ref": "P",
"aa_start": 1293,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8531,
"cdna_start": 3879,
"cds_end": null,
"cds_length": 5919,
"cds_start": 3879,
"consequences": [
"synonymous_variant"
],
"exon_count": 41,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000358062.7",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.3879G>A",
"hgvs_p": "p.Pro1293Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000350765.3",
"strand": false,
"transcript": "ENST00000358062.7",
"transcript_support_level": 5
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1243,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7384,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3732,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 35,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_004021.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004012.2",
"strand": false,
"transcript": "NM_004021.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1243,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5209,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3732,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 35,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000474231.5",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000417123.1",
"strand": false,
"transcript": "ENST00000474231.5",
"transcript_support_level": 5
},
{
"aa_alt": "P",
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"aa_length": 1230,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7345,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3693,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 34,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_004022.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004013.2",
"strand": false,
"transcript": "NM_004022.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1230,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7339,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3693,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 34,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000359836.5",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000352894.1",
"strand": false,
"transcript": "ENST00000359836.5",
"transcript_support_level": 5
},
{
"aa_alt": "P",
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"aa_length": 1225,
"aa_ref": "P",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7416,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3678,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 36,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_004013.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004004.2",
"strand": false,
"transcript": "NM_004013.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
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"aa_length": 1225,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7410,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3678,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 36,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000378707.7",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000367979.3",
"strand": false,
"transcript": "ENST00000378707.7",
"transcript_support_level": 5
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1212,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7361,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3639,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 35,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000684130.1",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508037.1",
"strand": false,
"transcript": "ENST00000684130.1",
"transcript_support_level": null
},
{
"aa_alt": "P",
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"aa_ref": "P",
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"biotype": "protein_coding",
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"cdna_end": null,
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"cdna_start": 2694,
"cds_end": null,
"cds_length": 3465,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 33,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000620040.5",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000478150.2",
"strand": false,
"transcript": "ENST00000620040.5",
"transcript_support_level": 5
},
{
"aa_alt": "P",
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"aa_ref": "P",
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"biotype": "protein_coding",
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"cdna_end": null,
"cdna_length": 7054,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3402,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 31,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_004023.3",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_004014.2",
"strand": false,
"transcript": "NM_004023.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7037,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3402,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 31,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000682238.1",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
"hgvs_c": "c.1653G>A",
"hgvs_p": "p.Pro551Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508124.1",
"strand": false,
"transcript": "ENST00000682238.1",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 1115,
"aa_ref": "P",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7086,
"cdna_start": 2694,
"cds_end": null,
"cds_length": 3348,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 32,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_004020.4",
"gene_hgnc_id": 2928,
"gene_symbol": "DMD",
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