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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: 1-112689610-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=112689610&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 112689610,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_020963.5",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "NM_001321324.2",
"protein_id": "NP_001308253.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000369645.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001321324.2"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000369645.6",
"protein_id": "ENSP00000358659.1",
"transcript_support_level": 5,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001321324.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000369645.6"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000357443.2",
"protein_id": "ENSP00000350028.2",
"transcript_support_level": 1,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000357443.2"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000413052.6",
"protein_id": "ENSP00000399797.2",
"transcript_support_level": 1,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000413052.6"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.369C>T",
"hgvs_p": "p.Phe123Phe",
"transcript": "ENST00000369644.5",
"protein_id": "ENSP00000358658.1",
"transcript_support_level": 1,
"aa_start": 123,
"aa_end": null,
"aa_length": 947,
"cds_start": 369,
"cds_end": null,
"cds_length": 2844,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000369644.5"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000885028.1",
"protein_id": "ENSP00000555087.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1045,
"cds_start": 537,
"cds_end": null,
"cds_length": 3138,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885028.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000686428.1",
"protein_id": "ENSP00000508727.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1023,
"cds_start": 537,
"cds_end": null,
"cds_length": 3072,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000686428.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000923700.1",
"protein_id": "ENSP00000593759.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1013,
"cds_start": 537,
"cds_end": null,
"cds_length": 3042,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923700.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "NM_001130079.3",
"protein_id": "NP_001123551.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130079.3"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "NM_001369507.1",
"protein_id": "NP_001356436.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001369507.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "NM_020963.5",
"protein_id": "NP_066014.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_020963.5"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000885023.1",
"protein_id": "ENSP00000555082.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885023.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000885025.1",
"protein_id": "ENSP00000555084.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885025.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000885027.1",
"protein_id": "ENSP00000555086.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885027.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000923694.1",
"protein_id": "ENSP00000593753.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923694.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000948326.1",
"protein_id": "ENSP00000618385.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 1003,
"cds_start": 537,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948326.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000948327.1",
"protein_id": "ENSP00000618386.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 999,
"cds_start": 537,
"cds_end": null,
"cds_length": 3000,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948327.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000923695.1",
"protein_id": "ENSP00000593754.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 984,
"cds_start": 537,
"cds_end": null,
"cds_length": 2955,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923695.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000923698.1",
"protein_id": "ENSP00000593757.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 978,
"cds_start": 537,
"cds_end": null,
"cds_length": 2937,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923698.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000885024.1",
"protein_id": "ENSP00000555083.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 958,
"cds_start": 537,
"cds_end": null,
"cds_length": 2877,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885024.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe",
"transcript": "ENST00000923699.1",
"protein_id": "ENSP00000593758.1",
"transcript_support_level": null,
"aa_start": 179,
"aa_end": null,
"aa_length": 958,
"cds_start": 537,
"cds_end": null,
"cds_length": 2877,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923699.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOV10",
"gene_hgnc_id": 7200,
"hgvs_c": "c.369C>T",
"hgvs_p": "p.Phe123Phe",
"transcript": "NM_001286072.2",
"protein_id": "NP_001273001.1",
"transcript_support_level": null,
"aa_start": 123,
"aa_end": null,
"aa_length": 947,
"cds_start": 369,
"cds_end": null,
"cds_length": 2844,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
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"inheritance_mode": "AD",
"hgvs_c": "c.537C>T",
"hgvs_p": "p.Phe179Phe"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}