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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: 3-18349633-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=18349633&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 18349633,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001195470.3",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_002971.6",
"protein_id": "NP_002962.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 3566,
"cdna_end": null,
"cdna_length": 7822,
"mane_select": "ENST00000338745.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002971.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000338745.11",
"protein_id": "ENSP00000341024.5",
"transcript_support_level": 1,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 3566,
"cdna_end": null,
"cdna_length": 7822,
"mane_select": "NM_002971.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000338745.11"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "ENST00000417717.6",
"protein_id": "ENSP00000399518.1",
"transcript_support_level": 1,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 2896,
"cdna_end": null,
"cdna_length": 4589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000417717.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000454909.6",
"protein_id": "ENSP00000399708.2",
"transcript_support_level": 1,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2062,
"cdna_end": null,
"cdna_length": 3755,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000454909.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "NM_001195470.3",
"protein_id": "NP_001182399.1",
"transcript_support_level": null,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 3662,
"cdna_end": null,
"cdna_length": 7918,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001195470.3"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "NM_001322871.2",
"protein_id": "NP_001309800.1",
"transcript_support_level": null,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 2215,
"cdna_end": null,
"cdna_length": 6471,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322871.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "ENST00000920137.1",
"protein_id": "ENSP00000590196.1",
"transcript_support_level": null,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 3509,
"cdna_end": null,
"cdna_length": 4415,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000920137.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "ENST00000941468.1",
"protein_id": "ENSP00000611527.1",
"transcript_support_level": null,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 2072,
"cdna_end": null,
"cdna_length": 3765,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941468.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1925C>G",
"hgvs_p": "p.Pro642Arg",
"transcript": "ENST00000941470.1",
"protein_id": "ENSP00000611529.1",
"transcript_support_level": null,
"aa_start": 642,
"aa_end": null,
"aa_length": 795,
"cds_start": 1925,
"cds_end": null,
"cds_length": 2388,
"cdna_start": 2197,
"cdna_end": null,
"cdna_length": 3103,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941470.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1919C>G",
"hgvs_p": "p.Pro640Arg",
"transcript": "ENST00000941471.1",
"protein_id": "ENSP00000611530.1",
"transcript_support_level": null,
"aa_start": 640,
"aa_end": null,
"aa_length": 793,
"cds_start": 1919,
"cds_end": null,
"cds_length": 2382,
"cdna_start": 2226,
"cdna_end": null,
"cdna_length": 3111,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941471.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_001131010.4",
"protein_id": "NP_001124482.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2025,
"cdna_end": null,
"cdna_length": 6281,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001131010.4"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_001322872.2",
"protein_id": "NP_001309801.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2114,
"cdna_end": null,
"cdna_length": 6370,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322872.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_001322873.2",
"protein_id": "NP_001309802.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2119,
"cdna_end": null,
"cdna_length": 6375,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322873.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_001322874.2",
"protein_id": "NP_001309803.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 1928,
"cdna_end": null,
"cdna_length": 6184,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322874.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "NM_001322875.2",
"protein_id": "NP_001309804.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 1922,
"cdna_end": null,
"cdna_length": 6178,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322875.2"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000415069.6",
"protein_id": "ENSP00000390529.2",
"transcript_support_level": 3,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 1957,
"cdna_end": null,
"cdna_length": 2702,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000415069.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000457005.6",
"protein_id": "ENSP00000398072.2",
"transcript_support_level": 4,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2004,
"cdna_end": null,
"cdna_length": 2467,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000457005.6"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000700177.1",
"protein_id": "ENSP00000514845.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
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"cdna_start": 2027,
"cdna_end": null,
"cdna_length": 3280,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000700177.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000700178.1",
"protein_id": "ENSP00000514846.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 1887,
"cdna_end": null,
"cdna_length": 3115,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000700178.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000700179.1",
"protein_id": "ENSP00000514847.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
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"cds_start": 1829,
"cds_end": null,
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"cdna_start": 2110,
"cdna_end": null,
"cdna_length": 3255,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000700179.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000700180.1",
"protein_id": "ENSP00000514848.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
"cds_end": null,
"cds_length": 2292,
"cdna_start": 2120,
"cdna_end": null,
"cdna_length": 2973,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000700180.1"
},
{
"aa_ref": "P",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SATB1",
"gene_hgnc_id": 10541,
"hgvs_c": "c.1829C>G",
"hgvs_p": "p.Pro610Arg",
"transcript": "ENST00000866365.1",
"protein_id": "ENSP00000536424.1",
"transcript_support_level": null,
"aa_start": 610,
"aa_end": null,
"aa_length": 763,
"cds_start": 1829,
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}