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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: 4-185587654-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=185587654&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 185587654,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001395207.1",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3876C>A",
"hgvs_p": "p.Phe1292Leu",
"transcript": "NM_001395207.1",
"protein_id": "NP_001382136.1",
"transcript_support_level": null,
"aa_start": 1292,
"aa_end": null,
"aa_length": 1300,
"cds_start": 3876,
"cds_end": null,
"cds_length": 3903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000695409.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001395207.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3876C>A",
"hgvs_p": "p.Phe1292Leu",
"transcript": "ENST00000695409.1",
"protein_id": "ENSP00000511888.1",
"transcript_support_level": null,
"aa_start": 1292,
"aa_end": null,
"aa_length": 1300,
"cds_start": 3876,
"cds_end": null,
"cds_length": 3903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001395207.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000695409.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3276C>A",
"hgvs_p": "p.Phe1092Leu",
"transcript": "ENST00000284776.11",
"protein_id": "ENSP00000284776.7",
"transcript_support_level": 1,
"aa_start": 1092,
"aa_end": null,
"aa_length": 1100,
"cds_start": 3276,
"cds_end": null,
"cds_length": 3303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000284776.11"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.2448C>A",
"hgvs_p": "p.Phe816Leu",
"transcript": "ENST00000437304.6",
"protein_id": "ENSP00000396008.2",
"transcript_support_level": 1,
"aa_start": 816,
"aa_end": null,
"aa_length": 824,
"cds_start": 2448,
"cds_end": null,
"cds_length": 2475,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000437304.6"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.2169C>A",
"hgvs_p": "p.Phe723Leu",
"transcript": "ENST00000319471.13",
"protein_id": "ENSP00000322182.9",
"transcript_support_level": 1,
"aa_start": 723,
"aa_end": null,
"aa_length": 731,
"cds_start": 2169,
"cds_end": null,
"cds_length": 2196,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000319471.13"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.1974C>A",
"hgvs_p": "p.Phe658Leu",
"transcript": "ENST00000393528.7",
"protein_id": "ENSP00000377162.3",
"transcript_support_level": 1,
"aa_start": 658,
"aa_end": null,
"aa_length": 666,
"cds_start": 1974,
"cds_end": null,
"cds_length": 2001,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393528.7"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.1908C>A",
"hgvs_p": "p.Phe636Leu",
"transcript": "ENST00000449407.6",
"protein_id": "ENSP00000397262.2",
"transcript_support_level": 1,
"aa_start": 636,
"aa_end": null,
"aa_length": 644,
"cds_start": 1908,
"cds_end": null,
"cds_length": 1935,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000449407.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "n.*2279C>A",
"hgvs_p": null,
"transcript": "ENST00000487184.2",
"protein_id": "ENSP00000511890.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000487184.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "n.*2279C>A",
"hgvs_p": null,
"transcript": "ENST00000487184.2",
"protein_id": "ENSP00000511890.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000487184.2"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.4692C>A",
"hgvs_p": "p.Phe1564Leu",
"transcript": "ENST00000421420.6",
"protein_id": "ENSP00000393258.2",
"transcript_support_level": 4,
"aa_start": 1564,
"aa_end": null,
"aa_length": 1572,
"cds_start": 4692,
"cds_end": null,
"cds_length": 4719,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000421420.6"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3834C>A",
"hgvs_p": "p.Phe1278Leu",
"transcript": "NM_001394245.1",
"protein_id": "NP_001381174.1",
"transcript_support_level": null,
"aa_start": 1278,
"aa_end": null,
"aa_length": 1286,
"cds_start": 3834,
"cds_end": null,
"cds_length": 3861,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394245.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3777C>A",
"hgvs_p": "p.Phe1259Leu",
"transcript": "NM_001394246.1",
"protein_id": "NP_001381175.1",
"transcript_support_level": null,
"aa_start": 1259,
"aa_end": null,
"aa_length": 1267,
"cds_start": 3777,
"cds_end": null,
"cds_length": 3804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394246.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3777C>A",
"hgvs_p": "p.Phe1259Leu",
"transcript": "NM_001394247.1",
"protein_id": "NP_001381176.1",
"transcript_support_level": null,
"aa_start": 1259,
"aa_end": null,
"aa_length": 1267,
"cds_start": 3777,
"cds_end": null,
"cds_length": 3804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394247.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3708C>A",
"hgvs_p": "p.Phe1236Leu",
"transcript": "NM_001394248.1",
"protein_id": "NP_001381177.1",
"transcript_support_level": null,
"aa_start": 1236,
"aa_end": null,
"aa_length": 1244,
"cds_start": 3708,
"cds_end": null,
"cds_length": 3735,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394248.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3708C>A",
"hgvs_p": "p.Phe1236Leu",
"transcript": "NM_001394249.1",
"protein_id": "NP_001381178.1",
"transcript_support_level": null,
"aa_start": 1236,
"aa_end": null,
"aa_length": 1244,
"cds_start": 3708,
"cds_end": null,
"cds_length": 3735,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394249.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3693C>A",
"hgvs_p": "p.Phe1231Leu",
"transcript": "NM_001394250.1",
"protein_id": "NP_001381179.1",
"transcript_support_level": null,
"aa_start": 1231,
"aa_end": null,
"aa_length": 1239,
"cds_start": 3693,
"cds_end": null,
"cds_length": 3720,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394250.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "NM_001270771.3",
"protein_id": "NP_001257700.1",
"transcript_support_level": null,
"aa_start": 1192,
"aa_end": null,
"aa_length": 1200,
"cds_start": 3576,
"cds_end": null,
"cds_length": 3603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001270771.3"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "NM_001394251.1",
"protein_id": "NP_001381180.1",
"transcript_support_level": null,
"aa_start": 1192,
"aa_end": null,
"aa_length": 1200,
"cds_start": 3576,
"cds_end": null,
"cds_length": 3603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394251.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "NM_001394252.1",
"protein_id": "NP_001381181.1",
"transcript_support_level": null,
"aa_start": 1192,
"aa_end": null,
"aa_length": 1200,
"cds_start": 3576,
"cds_end": null,
"cds_length": 3603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394252.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "NM_001394253.1",
"protein_id": "NP_001381182.1",
"transcript_support_level": null,
"aa_start": 1192,
"aa_end": null,
"aa_length": 1200,
"cds_start": 3576,
"cds_end": null,
"cds_length": 3603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394253.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "NM_001394254.1",
"protein_id": "NP_001381183.1",
"transcript_support_level": null,
"aa_start": 1192,
"aa_end": null,
"aa_length": 1200,
"cds_start": 3576,
"cds_end": null,
"cds_length": 3603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001394254.1"
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SORBS2",
"gene_hgnc_id": 24098,
"hgvs_c": "c.3576C>A",
"hgvs_p": "p.Phe1192Leu",
"transcript": "ENST00000355634.9",
"protein_id": "ENSP00000347852.5",
"transcript_support_level": 2,
"aa_start": 1192,
"aa_end": null,
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],
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"splice_prediction_selected": "Benign",
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"revel_prediction": "Uncertain_significance",
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"bayesdelnoaf_score": 0.09,
"bayesdelnoaf_prediction": "Uncertain_significance",
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"spliceai_max_prediction": "Benign",
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{
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"BS2"
],
"verdict": "Likely_benign",
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],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}