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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: 6-111334327-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=111334327&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 111334327,
"ref": "G",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000368802.8",
"consequences": [
{
"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": 32,
"intron_rank": 22,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7681-960C>T",
"hgvs_p": null,
"transcript": "NM_001372078.1",
"protein_id": "NP_001359007.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3130,
"cds_start": -4,
"cds_end": null,
"cds_length": 9393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10706,
"mane_select": "ENST00000368802.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 22,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7681-960C>T",
"hgvs_p": null,
"transcript": "ENST00000368802.8",
"protein_id": "ENSP00000357792.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 3130,
"cds_start": -4,
"cds_end": null,
"cds_length": 9393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10706,
"mane_select": "NM_001372078.1",
"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": 33,
"intron_rank": 23,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7681-960C>T",
"hgvs_p": null,
"transcript": "NM_002912.5",
"protein_id": "NP_002903.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3130,
"cds_start": -4,
"cds_end": null,
"cds_length": 9393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10830,
"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": 33,
"intron_rank": 23,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7681-960C>T",
"hgvs_p": null,
"transcript": "ENST00000358835.7",
"protein_id": "ENSP00000351697.3",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 3130,
"cds_start": -4,
"cds_end": null,
"cds_length": 9393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10815,
"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": 35,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7447-960C>T",
"hgvs_p": null,
"transcript": "NM_001286431.2",
"protein_id": "NP_001273360.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3052,
"cds_start": -4,
"cds_end": null,
"cds_length": 9159,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 11065,
"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": 34,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7447-960C>T",
"hgvs_p": null,
"transcript": "NM_001286432.2",
"protein_id": "NP_001273361.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3052,
"cds_start": -4,
"cds_end": null,
"cds_length": 9159,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10958,
"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": 34,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7447-960C>T",
"hgvs_p": null,
"transcript": "ENST00000435970.5",
"protein_id": "ENSP00000402003.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 3052,
"cds_start": -4,
"cds_end": null,
"cds_length": 9159,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10943,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "n.*7665-960C>T",
"hgvs_p": null,
"transcript": "ENST00000422377.5",
"protein_id": "ENSP00000393184.1",
"transcript_support_level": 2,
"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": 10964,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "n.*7772-960C>T",
"hgvs_p": null,
"transcript": "ENST00000434009.5",
"protein_id": "ENSP00000391605.1",
"transcript_support_level": 2,
"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": 10644,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MFSD4B",
"gene_hgnc_id": 21053,
"hgvs_c": "n.278-21456G>A",
"hgvs_p": null,
"transcript": "ENST00000666581.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 622,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MFSD4B",
"gene_hgnc_id": 21053,
"hgvs_c": "n.180-21456G>A",
"hgvs_p": null,
"transcript": "ENST00000673446.1",
"protein_id": null,
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"aa_start": null,
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"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 732,
"mane_select": null,
"mane_plus": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": 23,
"intron_rank_end": null,
"gene_symbol": "REV3L",
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"hgvs_c": "c.7762-960C>T",
"hgvs_p": null,
"transcript": "XM_011536028.3",
"protein_id": "XP_011534330.1",
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},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 33,
"intron_rank": 23,
"intron_rank_end": null,
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7759-960C>T",
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"transcript": "XM_011536029.4",
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},
{
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"strand": false,
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],
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"intron_rank": 22,
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7684-960C>T",
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},
{
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"intron_variant"
],
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7528-960C>T",
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"transcript": "XM_011536032.3",
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},
{
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"intron_variant"
],
"exon_rank": null,
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"exon_count": 30,
"intron_rank": 23,
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7762-960C>T",
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"transcript": "XM_047419215.1",
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},
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],
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7684-960C>T",
"hgvs_p": null,
"transcript": "XM_047419216.1",
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},
{
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"strand": false,
"consequences": [
"intron_variant"
],
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"intron_rank": 23,
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"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"hgvs_c": "c.7762-960C>T",
"hgvs_p": null,
"transcript": "XM_047419217.1",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 26,
"intron_rank": 23,
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7762-960C>T",
"hgvs_p": null,
"transcript": "XM_047419218.1",
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},
{
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"intron_variant"
],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 22,
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"gene_symbol": "REV3L",
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"hgvs_c": "c.7684-960C>T",
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"transcript": "XM_047419219.1",
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}
],
"gene_symbol": "REV3L",
"gene_hgnc_id": 9968,
"dbsnp": "rs465969",
"frequency_reference_population": 0.08690539,
"hom_count_reference_population": 613,
"allele_count_reference_population": 13227,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.0869054,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 13227,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 613,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.949999988079071,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.95,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.544,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000368802.8",
"gene_symbol": "REV3L",
"hgnc_id": 9968,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.7681-960C>T",
"hgvs_p": null
},
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000666581.2",
"gene_symbol": "MFSD4B",
"hgnc_id": 21053,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "n.278-21456G>A",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}