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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: 12-124782749-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=124782749&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 124782749,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_005505.5",
"consequences": [
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1464G>A",
"hgvs_p": "p.Gln488Gln",
"transcript": "NM_005505.5",
"protein_id": "NP_005496.4",
"transcript_support_level": null,
"aa_start": 488,
"aa_end": null,
"aa_length": 509,
"cds_start": 1464,
"cds_end": null,
"cds_length": 1530,
"cdna_start": 1608,
"cdna_end": null,
"cdna_length": 3405,
"mane_select": "ENST00000261693.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1464G>A",
"hgvs_p": "p.Gln488Gln",
"transcript": "ENST00000261693.11",
"protein_id": "ENSP00000261693.6",
"transcript_support_level": 1,
"aa_start": 488,
"aa_end": null,
"aa_length": 509,
"cds_start": 1464,
"cds_end": null,
"cds_length": 1530,
"cdna_start": 1608,
"cdna_end": null,
"cdna_length": 3405,
"mane_select": "NM_005505.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1380G>A",
"hgvs_p": "p.Gln460Gln",
"transcript": "ENST00000546215.5",
"protein_id": "ENSP00000442862.1",
"transcript_support_level": 1,
"aa_start": 460,
"aa_end": null,
"aa_length": 481,
"cds_start": 1380,
"cds_end": null,
"cds_length": 1446,
"cdna_start": 1443,
"cdna_end": null,
"cdna_length": 1597,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1779G>A",
"hgvs_p": null,
"transcript": "ENST00000535005.5",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1845,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1470G>A",
"hgvs_p": "p.Gln490Gln",
"transcript": "NM_001367983.1",
"protein_id": "NP_001354912.1",
"transcript_support_level": null,
"aa_start": 490,
"aa_end": null,
"aa_length": 511,
"cds_start": 1470,
"cds_end": null,
"cds_length": 1536,
"cdna_start": 1614,
"cdna_end": null,
"cdna_length": 3411,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1464G>A",
"hgvs_p": "p.Gln488Gln",
"transcript": "NM_001367989.1",
"protein_id": "NP_001354918.1",
"transcript_support_level": null,
"aa_start": 488,
"aa_end": null,
"aa_length": 509,
"cds_start": 1464,
"cds_end": null,
"cds_length": 1530,
"cdna_start": 1608,
"cdna_end": null,
"cdna_length": 3416,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1461G>A",
"hgvs_p": "p.Gln487Gln",
"transcript": "NM_001367984.1",
"protein_id": "NP_001354913.1",
"transcript_support_level": null,
"aa_start": 487,
"aa_end": null,
"aa_length": 508,
"cds_start": 1461,
"cds_end": null,
"cds_length": 1527,
"cdna_start": 1605,
"cdna_end": null,
"cdna_length": 3402,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1440G>A",
"hgvs_p": "p.Gln480Gln",
"transcript": "NM_001367985.1",
"protein_id": "NP_001354914.1",
"transcript_support_level": null,
"aa_start": 480,
"aa_end": null,
"aa_length": 501,
"cds_start": 1440,
"cds_end": null,
"cds_length": 1506,
"cdna_start": 1584,
"cdna_end": null,
"cdna_length": 3381,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1380G>A",
"hgvs_p": "p.Gln460Gln",
"transcript": "NM_001367986.1",
"protein_id": "NP_001354915.1",
"transcript_support_level": null,
"aa_start": 460,
"aa_end": null,
"aa_length": 481,
"cds_start": 1380,
"cds_end": null,
"cds_length": 1446,
"cdna_start": 1524,
"cdna_end": null,
"cdna_length": 3321,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1062G>A",
"hgvs_p": "p.Gln354Gln",
"transcript": "NM_001367988.1",
"protein_id": "NP_001354917.1",
"transcript_support_level": null,
"aa_start": 354,
"aa_end": null,
"aa_length": 375,
"cds_start": 1062,
"cds_end": null,
"cds_length": 1128,
"cdna_start": 1206,
"cdna_end": null,
"cdna_length": 3003,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.5152G>A",
"hgvs_p": null,
"transcript": "ENST00000538291.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5527,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.*583G>A",
"hgvs_p": null,
"transcript": "ENST00000681117.1",
"protein_id": "ENSP00000506693.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2493,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1337G>A",
"hgvs_p": null,
"transcript": "ENST00000681499.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2289,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1609G>A",
"hgvs_p": null,
"transcript": "NR_160416.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 3406,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1608G>A",
"hgvs_p": null,
"transcript": "NR_160417.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3508,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1534G>A",
"hgvs_p": null,
"transcript": "NR_160419.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1492G>A",
"hgvs_p": null,
"transcript": "NR_160422.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
"cdna_end": null,
"cdna_length": 3289,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.1489G>A",
"hgvs_p": null,
"transcript": "NR_160423.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3286,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "n.*583G>A",
"hgvs_p": null,
"transcript": "ENST00000681117.1",
"protein_id": "ENSP00000506693.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1651+3358G>A",
"hgvs_p": null,
"transcript": "NM_001367981.1",
"protein_id": "NP_001354910.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 552,
"cds_start": -4,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1651+3358G>A",
"hgvs_p": null,
"transcript": "ENST00000415380.6",
"protein_id": "ENSP00000414979.2",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 552,
"cds_start": -4,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
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"cdna_length": 2731,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1401+3608G>A",
"hgvs_p": null,
"transcript": "NM_001082959.2",
"protein_id": "NP_001076428.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 506,
"cds_start": -4,
"cds_end": null,
"cds_length": 1521,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3276,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "SCARB1",
"gene_hgnc_id": 1664,
"hgvs_c": "c.1401+3608G>A",
"hgvs_p": null,
"transcript": "ENST00000339570.9",
"protein_id": "ENSP00000343795.4",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 506,
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"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Likely benign",
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}
],
"message": null
}