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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: 17-75238705-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=75238705&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 75238705,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_138619.4",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.2008A>C",
"hgvs_p": "p.Ile670Leu",
"transcript": "NM_138619.4",
"protein_id": "NP_619525.1",
"transcript_support_level": null,
"aa_start": 670,
"aa_end": null,
"aa_length": 723,
"cds_start": 2008,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000537686.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_138619.4"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.2008A>C",
"hgvs_p": "p.Ile670Leu",
"transcript": "ENST00000537686.6",
"protein_id": "ENSP00000438085.3",
"transcript_support_level": 1,
"aa_start": 670,
"aa_end": null,
"aa_length": 723,
"cds_start": 2008,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_138619.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000537686.6"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1909A>C",
"hgvs_p": "p.Ile637Leu",
"transcript": "ENST00000538886.5",
"protein_id": "ENSP00000446421.2",
"transcript_support_level": 1,
"aa_start": 637,
"aa_end": null,
"aa_length": 690,
"cds_start": 1909,
"cds_end": null,
"cds_length": 2073,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000538886.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "n.*1967A>C",
"hgvs_p": null,
"transcript": "ENST00000621870.4",
"protein_id": "ENSP00000479464.1",
"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": "ENST00000621870.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "n.*1967A>C",
"hgvs_p": null,
"transcript": "ENST00000621870.4",
"protein_id": "ENSP00000479464.1",
"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": "ENST00000621870.4"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.2008A>C",
"hgvs_p": "p.Ile670Leu",
"transcript": "ENST00000924703.1",
"protein_id": "ENSP00000594762.1",
"transcript_support_level": null,
"aa_start": 670,
"aa_end": null,
"aa_length": 723,
"cds_start": 2008,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924703.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.2008A>C",
"hgvs_p": "p.Ile670Leu",
"transcript": "ENST00000924699.1",
"protein_id": "ENSP00000594758.1",
"transcript_support_level": null,
"aa_start": 670,
"aa_end": null,
"aa_length": 721,
"cds_start": 2008,
"cds_end": null,
"cds_length": 2166,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924699.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1987A>C",
"hgvs_p": "p.Ile663Leu",
"transcript": "ENST00000924706.1",
"protein_id": "ENSP00000594765.1",
"transcript_support_level": null,
"aa_start": 663,
"aa_end": null,
"aa_length": 716,
"cds_start": 1987,
"cds_end": null,
"cds_length": 2151,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924706.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1948A>C",
"hgvs_p": "p.Ile650Leu",
"transcript": "ENST00000924702.1",
"protein_id": "ENSP00000594761.1",
"transcript_support_level": null,
"aa_start": 650,
"aa_end": null,
"aa_length": 703,
"cds_start": 1948,
"cds_end": null,
"cds_length": 2112,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924702.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1942A>C",
"hgvs_p": "p.Ile648Leu",
"transcript": "ENST00000955609.1",
"protein_id": "ENSP00000625668.1",
"transcript_support_level": null,
"aa_start": 648,
"aa_end": null,
"aa_length": 701,
"cds_start": 1942,
"cds_end": null,
"cds_length": 2106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000955609.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1909A>C",
"hgvs_p": "p.Ile637Leu",
"transcript": "NM_014001.5",
"protein_id": "NP_054720.1",
"transcript_support_level": null,
"aa_start": 637,
"aa_end": null,
"aa_length": 690,
"cds_start": 1909,
"cds_end": null,
"cds_length": 2073,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014001.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1909A>C",
"hgvs_p": "p.Ile637Leu",
"transcript": "ENST00000924705.1",
"protein_id": "ENSP00000594764.1",
"transcript_support_level": null,
"aa_start": 637,
"aa_end": null,
"aa_length": 688,
"cds_start": 1909,
"cds_end": null,
"cds_length": 2067,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924705.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1843A>C",
"hgvs_p": "p.Ile615Leu",
"transcript": "ENST00000924704.1",
"protein_id": "ENSP00000594763.1",
"transcript_support_level": null,
"aa_start": 615,
"aa_end": null,
"aa_length": 668,
"cds_start": 1843,
"cds_end": null,
"cds_length": 2007,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924704.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1825A>C",
"hgvs_p": "p.Ile609Leu",
"transcript": "ENST00000924701.1",
"protein_id": "ENSP00000594760.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 662,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1989,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924701.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1792A>C",
"hgvs_p": "p.Ile598Leu",
"transcript": "NM_001172703.3",
"protein_id": "NP_001166174.1",
"transcript_support_level": null,
"aa_start": 598,
"aa_end": null,
"aa_length": 651,
"cds_start": 1792,
"cds_end": null,
"cds_length": 1956,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001172703.3"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1792A>C",
"hgvs_p": "p.Ile598Leu",
"transcript": "NM_001291641.2",
"protein_id": "NP_001278570.1",
"transcript_support_level": null,
"aa_start": 598,
"aa_end": null,
"aa_length": 651,
"cds_start": 1792,
"cds_end": null,
"cds_length": 1956,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291641.2"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1792A>C",
"hgvs_p": "p.Ile598Leu",
"transcript": "ENST00000582717.5",
"protein_id": "ENSP00000462081.1",
"transcript_support_level": 2,
"aa_start": 598,
"aa_end": null,
"aa_length": 651,
"cds_start": 1792,
"cds_end": null,
"cds_length": 1956,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000582717.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1786A>C",
"hgvs_p": "p.Ile596Leu",
"transcript": "ENST00000878323.1",
"protein_id": "ENSP00000548382.1",
"transcript_support_level": null,
"aa_start": 596,
"aa_end": null,
"aa_length": 649,
"cds_start": 1786,
"cds_end": null,
"cds_length": 1950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878323.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1792A>C",
"hgvs_p": "p.Ile598Leu",
"transcript": "ENST00000582486.5",
"protein_id": "ENSP00000462629.1",
"transcript_support_level": 5,
"aa_start": 598,
"aa_end": null,
"aa_length": 632,
"cds_start": 1792,
"cds_end": null,
"cds_length": 1899,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000582486.5"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1726A>C",
"hgvs_p": "p.Ile576Leu",
"transcript": "ENST00000924707.1",
"protein_id": "ENSP00000594766.1",
"transcript_support_level": null,
"aa_start": 576,
"aa_end": null,
"aa_length": 629,
"cds_start": 1726,
"cds_end": null,
"cds_length": 1890,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924707.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1708A>C",
"hgvs_p": "p.Ile570Leu",
"transcript": "ENST00000955610.1",
"protein_id": "ENSP00000625669.1",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 623,
"cds_start": 1708,
"cds_end": null,
"cds_length": 1872,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000955610.1"
},
{
"aa_ref": "I",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GGA3",
"gene_hgnc_id": 17079,
"hgvs_c": "c.1645A>C",
"hgvs_p": "p.Ile549Leu",
"transcript": "ENST00000924698.1",
"protein_id": "ENSP00000594757.1",
"transcript_support_level": null,
"aa_start": 549,
"aa_end": null,
"aa_length": 602,
"cds_start": 1645,
"cds_end": null,
"cds_length": 1809,
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{
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],
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"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
}