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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: 8-144356181-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=144356181&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "8",
"pos": 144356181,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_012162.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1259C>G",
"hgvs_p": "p.Thr420Arg",
"transcript": "NM_012162.4",
"protein_id": "NP_036294.2",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
"aa_length": 539,
"cds_start": 1259,
"cds_end": null,
"cds_length": 1620,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000331890.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012162.4"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1259C>G",
"hgvs_p": "p.Thr420Arg",
"transcript": "ENST00000331890.6",
"protein_id": "ENSP00000330098.5",
"transcript_support_level": 1,
"aa_start": 420,
"aa_end": null,
"aa_length": 539,
"cds_start": 1259,
"cds_end": null,
"cds_length": 1620,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_012162.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000331890.6"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1241C>G",
"hgvs_p": "p.Thr414Arg",
"transcript": "ENST00000455319.6",
"protein_id": "ENSP00000403873.2",
"transcript_support_level": 1,
"aa_start": 414,
"aa_end": null,
"aa_length": 533,
"cds_start": 1241,
"cds_end": null,
"cds_length": 1602,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000455319.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "n.2647C>G",
"hgvs_p": null,
"transcript": "ENST00000530142.5",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000530142.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1241C>G",
"hgvs_p": "p.Thr414Arg",
"transcript": "NM_024555.6",
"protein_id": "NP_078831.4",
"transcript_support_level": null,
"aa_start": 414,
"aa_end": null,
"aa_length": 533,
"cds_start": 1241,
"cds_end": null,
"cds_length": 1602,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_024555.6"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1223C>G",
"hgvs_p": "p.Thr408Arg",
"transcript": "ENST00000876698.1",
"protein_id": "ENSP00000546757.1",
"transcript_support_level": null,
"aa_start": 408,
"aa_end": null,
"aa_length": 527,
"cds_start": 1223,
"cds_end": null,
"cds_length": 1584,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876698.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1223C>G",
"hgvs_p": "p.Thr408Arg",
"transcript": "ENST00000948084.1",
"protein_id": "ENSP00000618143.1",
"transcript_support_level": null,
"aa_start": 408,
"aa_end": null,
"aa_length": 527,
"cds_start": 1223,
"cds_end": null,
"cds_length": 1584,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948084.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1220C>G",
"hgvs_p": "p.Thr407Arg",
"transcript": "ENST00000876699.1",
"protein_id": "ENSP00000546758.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 526,
"cds_start": 1220,
"cds_end": null,
"cds_length": 1581,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876699.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1217C>G",
"hgvs_p": "p.Thr406Arg",
"transcript": "ENST00000876697.1",
"protein_id": "ENSP00000546756.1",
"transcript_support_level": null,
"aa_start": 406,
"aa_end": null,
"aa_length": 525,
"cds_start": 1217,
"cds_end": null,
"cds_length": 1578,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876697.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1178C>G",
"hgvs_p": "p.Thr393Arg",
"transcript": "ENST00000913928.1",
"protein_id": "ENSP00000583987.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 512,
"cds_start": 1178,
"cds_end": null,
"cds_length": 1539,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913928.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1160C>G",
"hgvs_p": "p.Thr387Arg",
"transcript": "ENST00000876696.1",
"protein_id": "ENSP00000546755.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 506,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1521,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876696.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1145C>G",
"hgvs_p": "p.Thr382Arg",
"transcript": "ENST00000948083.1",
"protein_id": "ENSP00000618142.1",
"transcript_support_level": null,
"aa_start": 382,
"aa_end": null,
"aa_length": 501,
"cds_start": 1145,
"cds_end": null,
"cds_length": 1506,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948083.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1127C>G",
"hgvs_p": "p.Thr376Arg",
"transcript": "ENST00000913929.1",
"protein_id": "ENSP00000583988.1",
"transcript_support_level": null,
"aa_start": 376,
"aa_end": null,
"aa_length": 495,
"cds_start": 1127,
"cds_end": null,
"cds_length": 1488,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913929.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1100C>G",
"hgvs_p": "p.Thr367Arg",
"transcript": "ENST00000876701.1",
"protein_id": "ENSP00000546760.1",
"transcript_support_level": null,
"aa_start": 367,
"aa_end": null,
"aa_length": 486,
"cds_start": 1100,
"cds_end": null,
"cds_length": 1461,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876701.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1082C>G",
"hgvs_p": "p.Thr361Arg",
"transcript": "ENST00000948085.1",
"protein_id": "ENSP00000618144.1",
"transcript_support_level": null,
"aa_start": 361,
"aa_end": null,
"aa_length": 480,
"cds_start": 1082,
"cds_end": null,
"cds_length": 1443,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948085.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1046C>G",
"hgvs_p": "p.Thr349Arg",
"transcript": "ENST00000913930.1",
"protein_id": "ENSP00000583989.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 468,
"cds_start": 1046,
"cds_end": null,
"cds_length": 1407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913930.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.1037C>G",
"hgvs_p": "p.Thr346Arg",
"transcript": "ENST00000876700.1",
"protein_id": "ENSP00000546759.1",
"transcript_support_level": null,
"aa_start": 346,
"aa_end": null,
"aa_length": 465,
"cds_start": 1037,
"cds_end": null,
"cds_length": 1398,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876700.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.968C>G",
"hgvs_p": "p.Thr323Arg",
"transcript": "ENST00000913931.1",
"protein_id": "ENSP00000583990.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 442,
"cds_start": 968,
"cds_end": null,
"cds_length": 1329,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000913931.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.803C>G",
"hgvs_p": "p.Thr268Arg",
"transcript": "ENST00000876702.1",
"protein_id": "ENSP00000546761.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 387,
"cds_start": 803,
"cds_end": null,
"cds_length": 1164,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876702.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXL6",
"gene_hgnc_id": 13603,
"hgvs_c": "c.722C>G",
"hgvs_p": "p.Thr241Arg",
"transcript": "ENST00000948086.1",
"protein_id": "ENSP00000618145.1",
"transcript_support_level": null,
"aa_start": 241,
"aa_end": null,
"aa_length": 360,
"cds_start": 722,
"cds_end": null,
"cds_length": 1083,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948086.1"
},
{
"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": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SLC52A2",
"gene_hgnc_id": 30224,
"hgvs_c": "c.-462-1070G>C",
"hgvs_p": null,
"transcript": "ENST00000532815.2",
"protein_id": "ENSP00000501933.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 445,
"cds_start": null,
"cds_end": null,
"cds_length": 1338,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000532815.2"
},
{
"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": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SLC52A2",
"gene_hgnc_id": 30224,
"hgvs_c": "c.-111+798G>C",
"hgvs_p": null,
"transcript": "ENST00000675292.1",
"protein_id": "ENSP00000502652.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 445,
"cds_start": null,
"cds_end": null,
"cds_length": 1338,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000675292.1"
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{
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}
],
"message": null
}