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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: 10-92111170-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=92111170&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 92111170,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_014912.5",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1478A>G",
"hgvs_p": "p.Glu493Gly",
"transcript": "NM_014912.5",
"protein_id": "NP_055727.3",
"transcript_support_level": null,
"aa_start": 493,
"aa_end": null,
"aa_length": 698,
"cds_start": 1478,
"cds_end": null,
"cds_length": 2097,
"cdna_start": 1642,
"cdna_end": null,
"cdna_length": 7781,
"mane_select": "ENST00000265997.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014912.5"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1478A>G",
"hgvs_p": "p.Glu493Gly",
"transcript": "ENST00000265997.5",
"protein_id": "ENSP00000265997.4",
"transcript_support_level": 1,
"aa_start": 493,
"aa_end": null,
"aa_length": 698,
"cds_start": 1478,
"cds_end": null,
"cds_length": 2097,
"cdna_start": 1642,
"cdna_end": null,
"cdna_length": 7781,
"mane_select": "NM_014912.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000265997.5"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "ENST00000412050.8",
"protein_id": "ENSP00000398310.2",
"transcript_support_level": 1,
"aa_start": 479,
"aa_end": null,
"aa_length": 684,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2055,
"cdna_start": 1525,
"cdna_end": null,
"cdna_length": 7664,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000412050.8"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1529A>G",
"hgvs_p": "p.Glu510Gly",
"transcript": "ENST00000903868.1",
"protein_id": "ENSP00000573927.1",
"transcript_support_level": null,
"aa_start": 510,
"aa_end": null,
"aa_length": 715,
"cds_start": 1529,
"cds_end": null,
"cds_length": 2148,
"cdna_start": 1657,
"cdna_end": null,
"cdna_length": 5283,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903868.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1529A>G",
"hgvs_p": "p.Glu510Gly",
"transcript": "ENST00000903872.1",
"protein_id": "ENSP00000573931.1",
"transcript_support_level": null,
"aa_start": 510,
"aa_end": null,
"aa_length": 715,
"cds_start": 1529,
"cds_end": null,
"cds_length": 2148,
"cdna_start": 1649,
"cdna_end": null,
"cdna_length": 5275,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903872.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1529A>G",
"hgvs_p": "p.Glu510Gly",
"transcript": "ENST00000903879.1",
"protein_id": "ENSP00000573938.1",
"transcript_support_level": null,
"aa_start": 510,
"aa_end": null,
"aa_length": 715,
"cds_start": 1529,
"cds_end": null,
"cds_length": 2148,
"cdna_start": 1866,
"cdna_end": null,
"cdna_length": 5492,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903879.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000903866.1",
"protein_id": "ENSP00000573925.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1672,
"cdna_end": null,
"cdna_length": 5508,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903866.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000903870.1",
"protein_id": "ENSP00000573929.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1684,
"cdna_end": null,
"cdna_length": 5310,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903870.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000903875.1",
"protein_id": "ENSP00000573934.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1673,
"cdna_end": null,
"cdna_length": 5299,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903875.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000903878.1",
"protein_id": "ENSP00000573937.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1637,
"cdna_end": null,
"cdna_length": 5262,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903878.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000903880.1",
"protein_id": "ENSP00000573939.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1828,
"cdna_end": null,
"cdna_length": 5454,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903880.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000946417.1",
"protein_id": "ENSP00000616476.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1976,
"cdna_end": null,
"cdna_length": 5570,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946417.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000946418.1",
"protein_id": "ENSP00000616477.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1658,
"cdna_end": null,
"cdna_length": 5850,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946418.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1505A>G",
"hgvs_p": "p.Glu502Gly",
"transcript": "ENST00000946420.1",
"protein_id": "ENSP00000616479.1",
"transcript_support_level": null,
"aa_start": 502,
"aa_end": null,
"aa_length": 707,
"cds_start": 1505,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1701,
"cdna_end": null,
"cdna_length": 5326,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946420.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1478A>G",
"hgvs_p": "p.Glu493Gly",
"transcript": "ENST00000614585.4",
"protein_id": "ENSP00000482128.1",
"transcript_support_level": 5,
"aa_start": 493,
"aa_end": null,
"aa_length": 698,
"cds_start": 1478,
"cds_end": null,
"cds_length": 2097,
"cdna_start": 1600,
"cdna_end": null,
"cdna_length": 5789,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000614585.4"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1460A>G",
"hgvs_p": "p.Glu487Gly",
"transcript": "ENST00000903882.1",
"protein_id": "ENSP00000573941.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 692,
"cds_start": 1460,
"cds_end": null,
"cds_length": 2079,
"cdna_start": 1520,
"cdna_end": null,
"cdna_length": 5146,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903882.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1448A>G",
"hgvs_p": "p.Glu483Gly",
"transcript": "ENST00000912186.1",
"protein_id": "ENSP00000582245.1",
"transcript_support_level": null,
"aa_start": 483,
"aa_end": null,
"aa_length": 688,
"cds_start": 1448,
"cds_end": null,
"cds_length": 2067,
"cdna_start": 1554,
"cdna_end": null,
"cdna_length": 5527,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912186.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "NM_001178137.2",
"protein_id": "NP_001171608.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 684,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2055,
"cdna_start": 1558,
"cdna_end": null,
"cdna_length": 7697,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001178137.2"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "ENST00000903860.1",
"protein_id": "ENSP00000573920.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 684,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2055,
"cdna_start": 1662,
"cdna_end": null,
"cdna_length": 5857,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903860.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "ENST00000903863.1",
"protein_id": "ENSP00000573922.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 684,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2055,
"cdna_start": 1603,
"cdna_end": null,
"cdna_length": 5576,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903863.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "ENST00000903874.1",
"protein_id": "ENSP00000573933.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 684,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2055,
"cdna_start": 1628,
"cdna_end": null,
"cdna_length": 5254,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903874.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CPEB3",
"gene_hgnc_id": 21746,
"hgvs_c": "c.1436A>G",
"hgvs_p": "p.Glu479Gly",
"transcript": "ENST00000903876.1",
"protein_id": "ENSP00000573935.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
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],
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"clinvar_classification": "Uncertain significance",
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"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}