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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: 1-1752977-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=1752977&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 1752977,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001198994.2",
"consequences": [
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "NM_023018.5",
"protein_id": "NP_075394.3",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000341426.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_023018.5"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": true,
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000341426.9",
"protein_id": "ENSP00000341679.5",
"transcript_support_level": 2,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_023018.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000341426.9"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1703A>G",
"hgvs_p": "p.Gln568Arg",
"transcript": "ENST00000378625.5",
"protein_id": "ENSP00000367890.1",
"transcript_support_level": 1,
"aa_start": 568,
"aa_end": null,
"aa_length": 591,
"cds_start": 1703,
"cds_end": null,
"cds_length": 1776,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000378625.5"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000341991.7",
"protein_id": "ENSP00000344340.3",
"transcript_support_level": 1,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000341991.7"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1703A>G",
"hgvs_p": "p.Gln568Arg",
"transcript": "NM_001198994.2",
"protein_id": "NP_001185923.1",
"transcript_support_level": null,
"aa_start": 568,
"aa_end": null,
"aa_length": 591,
"cds_start": 1703,
"cds_end": null,
"cds_length": 1776,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001198994.2"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1295A>G",
"hgvs_p": "p.Gln432Arg",
"transcript": "ENST00000886141.1",
"protein_id": "ENSP00000556200.1",
"transcript_support_level": null,
"aa_start": 432,
"aa_end": null,
"aa_length": 455,
"cds_start": 1295,
"cds_end": null,
"cds_length": 1368,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886141.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1289A>G",
"hgvs_p": "p.Gln430Arg",
"transcript": "ENST00000886139.1",
"protein_id": "ENSP00000556198.1",
"transcript_support_level": null,
"aa_start": 430,
"aa_end": null,
"aa_length": 453,
"cds_start": 1289,
"cds_end": null,
"cds_length": 1362,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886139.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1289A>G",
"hgvs_p": "p.Gln430Arg",
"transcript": "ENST00000931659.1",
"protein_id": "ENSP00000601718.1",
"transcript_support_level": null,
"aa_start": 430,
"aa_end": null,
"aa_length": 453,
"cds_start": 1289,
"cds_end": null,
"cds_length": 1362,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931659.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "NM_001198993.2",
"protein_id": "NP_001185922.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001198993.2"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "NM_001353641.2",
"protein_id": "NP_001340570.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001353641.2"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886130.1",
"protein_id": "ENSP00000556189.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886130.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886131.1",
"protein_id": "ENSP00000556190.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886131.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886132.1",
"protein_id": "ENSP00000556191.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886132.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886133.1",
"protein_id": "ENSP00000556192.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886133.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886134.1",
"protein_id": "ENSP00000556193.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886134.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886136.1",
"protein_id": "ENSP00000556195.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886136.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886137.1",
"protein_id": "ENSP00000556196.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886137.1"
},
{
"aa_ref": "Q",
"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": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886138.1",
"protein_id": "ENSP00000556197.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886138.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000886140.1",
"protein_id": "ENSP00000556199.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886140.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000931657.1",
"protein_id": "ENSP00000601716.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931657.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000931658.1",
"protein_id": "ENSP00000601717.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931658.1"
},
{
"aa_ref": "Q",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NADK",
"gene_hgnc_id": 29831,
"hgvs_c": "c.1268A>G",
"hgvs_p": "p.Gln423Arg",
"transcript": "ENST00000931660.1",
"protein_id": "ENSP00000601719.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 446,
"cds_start": 1268,
"cds_end": null,
"cds_length": 1341,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931660.1"
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"hgvs_p": "p.Gln568Arg"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}