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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: 5-150396792-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=150396792&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 150396792,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000643257.2",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4295G>C",
"hgvs_p": "p.Gly1432Ala",
"transcript": "NM_001371623.1",
"protein_id": "NP_001358552.1",
"transcript_support_level": null,
"aa_start": 1432,
"aa_end": null,
"aa_length": 1489,
"cds_start": 4295,
"cds_end": null,
"cds_length": 4470,
"cdna_start": 4345,
"cdna_end": null,
"cdna_length": 5026,
"mane_select": "ENST00000643257.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4295G>C",
"hgvs_p": "p.Gly1432Ala",
"transcript": "ENST00000643257.2",
"protein_id": "ENSP00000493815.1",
"transcript_support_level": null,
"aa_start": 1432,
"aa_end": null,
"aa_length": 1489,
"cds_start": 4295,
"cds_end": null,
"cds_length": 4470,
"cdna_start": 4345,
"cdna_end": null,
"cdna_length": 5026,
"mane_select": "NM_001371623.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4292G>C",
"hgvs_p": "p.Gly1431Ala",
"transcript": "ENST00000504761.6",
"protein_id": "ENSP00000421655.2",
"transcript_support_level": 1,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1488,
"cds_start": 4292,
"cds_end": null,
"cds_length": 4467,
"cdna_start": 4292,
"cdna_end": null,
"cdna_length": 4467,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4061G>C",
"hgvs_p": "p.Gly1354Ala",
"transcript": "ENST00000323668.11",
"protein_id": "ENSP00000325223.6",
"transcript_support_level": 1,
"aa_start": 1354,
"aa_end": null,
"aa_length": 1411,
"cds_start": 4061,
"cds_end": null,
"cds_length": 4236,
"cdna_start": 4136,
"cdna_end": null,
"cdna_length": 4832,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4292G>C",
"hgvs_p": "p.Gly1431Ala",
"transcript": "NM_001135243.2",
"protein_id": "NP_001128715.1",
"transcript_support_level": null,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1488,
"cds_start": 4292,
"cds_end": null,
"cds_length": 4467,
"cdna_start": 4342,
"cdna_end": null,
"cdna_length": 5023,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4292G>C",
"hgvs_p": "p.Gly1431Ala",
"transcript": "ENST00000377797.7",
"protein_id": "ENSP00000367028.4",
"transcript_support_level": 5,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1488,
"cds_start": 4292,
"cds_end": null,
"cds_length": 4467,
"cdna_start": 4400,
"cdna_end": null,
"cdna_length": 5095,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4292G>C",
"hgvs_p": "p.Gly1431Ala",
"transcript": "ENST00000513346.5",
"protein_id": "ENSP00000427484.1",
"transcript_support_level": 5,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1488,
"cds_start": 4292,
"cds_end": null,
"cds_length": 4467,
"cdna_start": 4292,
"cdna_end": null,
"cdna_length": 4646,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4181G>C",
"hgvs_p": "p.Gly1394Ala",
"transcript": "NM_001135244.2",
"protein_id": "NP_001128716.1",
"transcript_support_level": null,
"aa_start": 1394,
"aa_end": null,
"aa_length": 1451,
"cds_start": 4181,
"cds_end": null,
"cds_length": 4356,
"cdna_start": 4231,
"cdna_end": null,
"cdna_length": 4912,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4181G>C",
"hgvs_p": "p.Gly1394Ala",
"transcript": "ENST00000439160.6",
"protein_id": "ENSP00000406888.2",
"transcript_support_level": 5,
"aa_start": 1394,
"aa_end": null,
"aa_length": 1451,
"cds_start": 4181,
"cds_end": null,
"cds_length": 4356,
"cdna_start": 4214,
"cdna_end": null,
"cdna_length": 4644,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4178G>C",
"hgvs_p": "p.Gly1393Ala",
"transcript": "NM_001195141.2",
"protein_id": "NP_001182070.1",
"transcript_support_level": null,
"aa_start": 1393,
"aa_end": null,
"aa_length": 1450,
"cds_start": 4178,
"cds_end": null,
"cds_length": 4353,
"cdna_start": 4228,
"cdna_end": null,
"cdna_length": 4909,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4178G>C",
"hgvs_p": "p.Gly1393Ala",
"transcript": "ENST00000427724.7",
"protein_id": "ENSP00000390717.3",
"transcript_support_level": 5,
"aa_start": 1393,
"aa_end": null,
"aa_length": 1450,
"cds_start": 4178,
"cds_end": null,
"cds_length": 4353,
"cdna_start": 4206,
"cdna_end": null,
"cdna_length": 4800,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4064G>C",
"hgvs_p": "p.Gly1355Ala",
"transcript": "NM_001135245.2",
"protein_id": "NP_001128717.1",
"transcript_support_level": null,
"aa_start": 1355,
"aa_end": null,
"aa_length": 1412,
"cds_start": 4064,
"cds_end": null,
"cds_length": 4239,
"cdna_start": 4114,
"cdna_end": null,
"cdna_length": 4795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4064G>C",
"hgvs_p": "p.Gly1355Ala",
"transcript": "ENST00000445265.6",
"protein_id": "ENSP00000409944.2",
"transcript_support_level": 5,
"aa_start": 1355,
"aa_end": null,
"aa_length": 1412,
"cds_start": 4064,
"cds_end": null,
"cds_length": 4239,
"cdna_start": 4145,
"cdna_end": null,
"cdna_length": 4825,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4061G>C",
"hgvs_p": "p.Gly1354Ala",
"transcript": "NM_000356.4",
"protein_id": "NP_000347.2",
"transcript_support_level": null,
"aa_start": 1354,
"aa_end": null,
"aa_length": 1411,
"cds_start": 4061,
"cds_end": null,
"cds_length": 4236,
"cdna_start": 4111,
"cdna_end": null,
"cdna_length": 4792,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4061G>C",
"hgvs_p": "p.Gly1354Ala",
"transcript": "NM_001437406.1",
"protein_id": "NP_001424335.1",
"transcript_support_level": null,
"aa_start": 1354,
"aa_end": null,
"aa_length": 1411,
"cds_start": 4061,
"cds_end": null,
"cds_length": 4236,
"cdna_start": 4111,
"cdna_end": null,
"cdna_length": 4792,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.3950G>C",
"hgvs_p": "p.Gly1317Ala",
"transcript": "ENST00000650162.1",
"protein_id": "ENSP00000497075.1",
"transcript_support_level": null,
"aa_start": 1317,
"aa_end": null,
"aa_length": 1357,
"cds_start": 3950,
"cds_end": null,
"cds_length": 4076,
"cdna_start": 4068,
"cdna_end": null,
"cdna_length": 4194,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.3692G>C",
"hgvs_p": "p.Gly1231Ala",
"transcript": "ENST00000674413.1",
"protein_id": "ENSP00000501343.1",
"transcript_support_level": null,
"aa_start": 1231,
"aa_end": null,
"aa_length": 1238,
"cds_start": 3692,
"cds_end": null,
"cds_length": 3719,
"cdna_start": 3694,
"cdna_end": null,
"cdna_length": 3726,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.392G>C",
"hgvs_p": "p.Gly131Ala",
"transcript": "ENST00000515516.1",
"protein_id": "ENSP00000426471.1",
"transcript_support_level": 5,
"aa_start": 131,
"aa_end": null,
"aa_length": 188,
"cds_start": 392,
"cds_end": null,
"cds_length": 567,
"cdna_start": 392,
"cdna_end": null,
"cdna_length": 661,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4406G>C",
"hgvs_p": "p.Gly1469Ala",
"transcript": "XM_005268502.5",
"protein_id": "XP_005268559.1",
"transcript_support_level": null,
"aa_start": 1469,
"aa_end": null,
"aa_length": 1526,
"cds_start": 4406,
"cds_end": null,
"cds_length": 4581,
"cdna_start": 4456,
"cdna_end": null,
"cdna_length": 5137,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4403G>C",
"hgvs_p": "p.Gly1468Ala",
"transcript": "XM_005268503.5",
"protein_id": "XP_005268560.1",
"transcript_support_level": null,
"aa_start": 1468,
"aa_end": null,
"aa_length": 1525,
"cds_start": 4403,
"cds_end": null,
"cds_length": 4578,
"cdna_start": 4453,
"cdna_end": null,
"cdna_length": 5134,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4403G>C",
"hgvs_p": "p.Gly1468Ala",
"transcript": "XM_005268504.5",
"protein_id": "XP_005268561.1",
"transcript_support_level": null,
"aa_start": 1468,
"aa_end": null,
"aa_length": 1525,
"cds_start": 4403,
"cds_end": null,
"cds_length": 4578,
"cdna_start": 4453,
"cdna_end": null,
"cdna_length": 5134,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCOF1",
"gene_hgnc_id": 11654,
"hgvs_c": "c.4400G>C",
"hgvs_p": "p.Gly1467Ala",
"transcript": "XM_047417645.1",
"protein_id": "XP_047273601.1",
"transcript_support_level": null,
"aa_start": 1467,
"aa_end": null,
"aa_length": 1524,
"cds_start": 4400,
"cds_end": null,
"cds_length": 4575,
"cdna_start": 4450,
"cdna_end": null,
"cdna_length": 5131,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 27,
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],
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"computational_prediction_selected": "Benign",
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"splice_prediction_selected": "Benign",
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"bayesdelnoaf_score": -0.18,
"bayesdelnoaf_prediction": "Benign",
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"acmg_by_gene": [
{
"score": -20,
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"criteria": [
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"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000643257.2",
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"effects": [
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],
"inheritance_mode": "AD",
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],
"clinvar_disease": "Treacher Collins syndrome 1,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:5",
"phenotype_combined": "not specified|Treacher Collins syndrome 1|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}