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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: 2-219077304-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=219077304&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 219077304,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001377499.1",
"consequences": [
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "NM_024782.3",
"protein_id": "NP_079058.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000356853.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_024782.3"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000356853.10",
"protein_id": "ENSP00000349313.5",
"transcript_support_level": 1,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_024782.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000356853.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000280537",
"gene_hgnc_id": null,
"hgvs_c": "n.*1889A>T",
"hgvs_p": null,
"transcript": "ENST00000318673.6",
"protein_id": "ENSP00000320919.3",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000318673.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000280537",
"gene_hgnc_id": null,
"hgvs_c": "n.*1889A>T",
"hgvs_p": null,
"transcript": "ENST00000318673.6",
"protein_id": "ENSP00000320919.3",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000318673.6"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.833A>T",
"hgvs_p": "p.Gln278Leu",
"transcript": "ENST00000881108.1",
"protein_id": "ENSP00000551167.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 321,
"cds_start": 833,
"cds_end": null,
"cds_length": 966,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881108.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000409720.5",
"protein_id": "ENSP00000387290.1",
"transcript_support_level": 5,
"aa_start": 256,
"aa_end": null,
"aa_length": 316,
"cds_start": 767,
"cds_end": null,
"cds_length": 951,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409720.5"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.782A>T",
"hgvs_p": "p.Gln261Leu",
"transcript": "NM_001377499.1",
"protein_id": "NP_001364428.1",
"transcript_support_level": null,
"aa_start": 261,
"aa_end": null,
"aa_length": 304,
"cds_start": 782,
"cds_end": null,
"cds_length": 915,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001377499.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.782A>T",
"hgvs_p": "p.Gln261Leu",
"transcript": "ENST00000426304.6",
"protein_id": "ENSP00000394896.2",
"transcript_support_level": 3,
"aa_start": 261,
"aa_end": null,
"aa_length": 304,
"cds_start": 782,
"cds_end": null,
"cds_length": 915,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000426304.6"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.782A>T",
"hgvs_p": "p.Gln261Leu",
"transcript": "ENST00000929435.1",
"protein_id": "ENSP00000599494.1",
"transcript_support_level": null,
"aa_start": 261,
"aa_end": null,
"aa_length": 304,
"cds_start": 782,
"cds_end": null,
"cds_length": 915,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929435.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.782A>T",
"hgvs_p": "p.Gln261Leu",
"transcript": "ENST00000929436.1",
"protein_id": "ENSP00000599495.1",
"transcript_support_level": null,
"aa_start": 261,
"aa_end": null,
"aa_length": 304,
"cds_start": 782,
"cds_end": null,
"cds_length": 915,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929436.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "NM_001377498.1",
"protein_id": "NP_001364427.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001377498.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000457600.3",
"protein_id": "ENSP00000407201.2",
"transcript_support_level": 3,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000457600.3"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000881109.1",
"protein_id": "ENSP00000551168.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000881109.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000929432.1",
"protein_id": "ENSP00000599491.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929432.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000929437.1",
"protein_id": "ENSP00000599496.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929437.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.767A>T",
"hgvs_p": "p.Gln256Leu",
"transcript": "ENST00000929438.1",
"protein_id": "ENSP00000599497.1",
"transcript_support_level": null,
"aa_start": 256,
"aa_end": null,
"aa_length": 299,
"cds_start": 767,
"cds_end": null,
"cds_length": 900,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929438.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.764A>T",
"hgvs_p": "p.Gln255Leu",
"transcript": "ENST00000929433.1",
"protein_id": "ENSP00000599492.1",
"transcript_support_level": null,
"aa_start": 255,
"aa_end": null,
"aa_length": 298,
"cds_start": 764,
"cds_end": null,
"cds_length": 897,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929433.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.764A>T",
"hgvs_p": "p.Gln255Leu",
"transcript": "ENST00000929434.1",
"protein_id": "ENSP00000599493.1",
"transcript_support_level": null,
"aa_start": 255,
"aa_end": null,
"aa_length": 298,
"cds_start": 764,
"cds_end": null,
"cds_length": 897,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929434.1"
},
{
"aa_ref": "Q",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "c.554A>T",
"hgvs_p": "p.Gln185Leu",
"transcript": "ENST00000941811.1",
"protein_id": "ENSP00000611870.1",
"transcript_support_level": null,
"aa_start": 185,
"aa_end": null,
"aa_length": 228,
"cds_start": 554,
"cds_end": null,
"cds_length": 687,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941811.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "n.*150A>T",
"hgvs_p": null,
"transcript": "ENST00000418099.5",
"protein_id": "ENSP00000408966.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000418099.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "n.451A>T",
"hgvs_p": null,
"transcript": "ENST00000483627.1",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000483627.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NHEJ1",
"gene_hgnc_id": 25737,
"hgvs_c": "n.376A>T",
"hgvs_p": null,
"transcript": "ENST00000491159.5",
"protein_id": null,
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
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"computational_score_selected": 0.004150658845901489,
"computational_prediction_selected": "Benign",
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"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.161,
"revel_prediction": "Benign",
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"bayesdelnoaf_score": -0.35,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.304,
"phylop100way_prediction": "Benign",
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"spliceai_max_prediction": "Benign",
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"acmg_score": -20,
"acmg_classification": "Benign",
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"acmg_by_gene": [
{
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"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
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"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001377499.1",
"gene_symbol": "NHEJ1",
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"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.782A>T",
"hgvs_p": "p.Gln261Leu"
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{
"score": -20,
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"criteria": [
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"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000318673.6",
"gene_symbol": "ENSG00000280537",
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"effects": [
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],
"inheritance_mode": "",
"hgvs_c": "n.*1889A>T",
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}
],
"clinvar_disease": "Cernunnos-XLF deficiency,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:3",
"phenotype_combined": "not specified|Cernunnos-XLF deficiency|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}