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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: 13-108211235-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=108211235&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "13",
"pos": 108211235,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000442234.6",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_206937.2",
"protein_id": "NP_996820.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 188,
"cdna_end": null,
"cdna_length": 3981,
"mane_select": "ENST00000442234.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000442234.6",
"protein_id": "ENSP00000402030.1",
"transcript_support_level": 1,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 188,
"cdna_end": null,
"cdna_length": 3981,
"mane_select": "NM_206937.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000405925.2",
"protein_id": "ENSP00000385955.1",
"transcript_support_level": 1,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 269,
"cdna_end": null,
"cdna_length": 4065,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001098268.2",
"protein_id": "NP_001091738.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 250,
"cdna_end": null,
"cdna_length": 4043,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352598.2",
"protein_id": "NP_001339527.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 4460,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352599.2",
"protein_id": "NP_001339528.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 691,
"cdna_end": null,
"cdna_length": 4484,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352600.2",
"protein_id": "NP_001339529.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 583,
"cdna_end": null,
"cdna_length": 4376,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352601.2",
"protein_id": "NP_001339530.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 292,
"cdna_end": null,
"cdna_length": 4085,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352602.2",
"protein_id": "NP_001339531.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 184,
"cdna_end": null,
"cdna_length": 3977,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001352603.1",
"protein_id": "NP_001339532.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 162,
"cdna_end": null,
"cdna_length": 3955,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_001379095.1",
"protein_id": "NP_001366024.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
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"cds_length": 2736,
"cdna_start": 385,
"cdna_end": null,
"cdna_length": 4178,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "NM_002312.3",
"protein_id": "NP_002303.2",
"transcript_support_level": null,
"aa_start": 12,
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"aa_length": 911,
"cds_start": 34,
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"cdna_start": 307,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000611712.4",
"protein_id": "ENSP00000484288.1",
"transcript_support_level": 4,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
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"cdna_start": 384,
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 3,
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"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000685338.1",
"protein_id": "ENSP00000510567.1",
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},
{
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],
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"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000686095.1",
"protein_id": "ENSP00000509942.1",
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"aa_start": 12,
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"cds_start": 34,
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"cdna_start": 270,
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"mane_select": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 3,
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"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000686204.1",
"protein_id": "ENSP00000509685.1",
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},
{
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],
"exon_rank": 3,
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"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "LIG4",
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"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000686913.1",
"protein_id": "ENSP00000509299.1",
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},
{
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"consequences": [
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],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000686926.1",
"protein_id": "ENSP00000509122.1",
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"aa_end": null,
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},
{
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],
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
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"transcript": "ENST00000687164.1",
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},
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],
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"intron_rank": null,
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"gene_symbol": "LIG4",
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"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000687822.1",
"protein_id": "ENSP00000509344.1",
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},
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"consequences": [
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],
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"intron_rank": null,
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"gene_symbol": "LIG4",
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"hgvs_c": "c.34T>G",
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"transcript": "ENST00000688396.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000688455.1",
"protein_id": "ENSP00000509304.1",
"transcript_support_level": null,
"aa_start": 12,
"aa_end": null,
"aa_length": 911,
"cds_start": 34,
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"cdna_start": 573,
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"cdna_length": 4348,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "LIG4",
"gene_hgnc_id": 6601,
"hgvs_c": "c.34T>G",
"hgvs_p": "p.Ser12Ala",
"transcript": "ENST00000688529.1",
"protein_id": "ENSP00000509906.1",
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{
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],
"clinvar_disease": "DNA ligase IV deficiency",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "DNA ligase IV deficiency",
"pathogenicity_classification_combined": "Uncertain significance",
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}
],
"message": null
}