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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: 1-97699535-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=97699535&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 97699535,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_000110.4",
"consequences": [
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "NM_000110.4",
"protein_id": "NP_000101.2",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1025,
"cds_start": 496,
"cds_end": null,
"cds_length": 3078,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4423,
"mane_select": "ENST00000370192.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000110.4"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000370192.8",
"protein_id": "ENSP00000359211.3",
"transcript_support_level": 1,
"aa_start": 166,
"aa_end": null,
"aa_length": 1025,
"cds_start": 496,
"cds_end": null,
"cds_length": 3078,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4423,
"mane_select": "NM_000110.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000370192.8"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876340.1",
"protein_id": "ENSP00000546399.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1081,
"cds_start": 496,
"cds_end": null,
"cds_length": 3246,
"cdna_start": 603,
"cdna_end": null,
"cdna_length": 4583,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876340.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000969915.1",
"protein_id": "ENSP00000639974.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1060,
"cds_start": 496,
"cds_end": null,
"cds_length": 3183,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4525,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969915.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876335.1",
"protein_id": "ENSP00000546394.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1058,
"cds_start": 496,
"cds_end": null,
"cds_length": 3177,
"cdna_start": 614,
"cdna_end": null,
"cdna_length": 4528,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876335.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000969914.1",
"protein_id": "ENSP00000639973.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1055,
"cds_start": 496,
"cds_end": null,
"cds_length": 3168,
"cdna_start": 626,
"cdna_end": null,
"cdna_length": 4527,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969914.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876334.1",
"protein_id": "ENSP00000546393.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 1002,
"cds_start": 496,
"cds_end": null,
"cds_length": 3009,
"cdna_start": 631,
"cdna_end": null,
"cdna_length": 4374,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876334.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876341.1",
"protein_id": "ENSP00000546400.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 993,
"cds_start": 496,
"cds_end": null,
"cds_length": 2982,
"cdna_start": 535,
"cdna_end": null,
"cdna_length": 4254,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876341.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.385A>G",
"hgvs_p": "p.Met129Val",
"transcript": "ENST00000876339.1",
"protein_id": "ENSP00000546398.1",
"transcript_support_level": null,
"aa_start": 129,
"aa_end": null,
"aa_length": 988,
"cds_start": 385,
"cds_end": null,
"cds_length": 2967,
"cdna_start": 492,
"cdna_end": null,
"cdna_length": 4307,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876339.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876337.1",
"protein_id": "ENSP00000546396.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 985,
"cds_start": 496,
"cds_end": null,
"cds_length": 2958,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4303,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876337.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876336.1",
"protein_id": "ENSP00000546395.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 978,
"cds_start": 496,
"cds_end": null,
"cds_length": 2937,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4282,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876336.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "ENST00000876338.1",
"protein_id": "ENSP00000546397.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 953,
"cds_start": 496,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 4207,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000876338.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.385A>G",
"hgvs_p": "p.Met129Val",
"transcript": "XM_017000507.2",
"protein_id": "XP_016855996.1",
"transcript_support_level": null,
"aa_start": 129,
"aa_end": null,
"aa_length": 988,
"cds_start": 385,
"cds_end": null,
"cds_length": 2967,
"cdna_start": 522,
"cdna_end": null,
"cdna_length": 4337,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000507.2"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "XM_005270562.3",
"protein_id": "XP_005270619.2",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 953,
"cds_start": 496,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 633,
"cdna_end": null,
"cdna_length": 4232,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005270562.3"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.268A>G",
"hgvs_p": "p.Met90Val",
"transcript": "XM_047448076.1",
"protein_id": "XP_047304032.1",
"transcript_support_level": null,
"aa_start": 90,
"aa_end": null,
"aa_length": 949,
"cds_start": 268,
"cds_end": null,
"cds_length": 2850,
"cdna_start": 526,
"cdna_end": null,
"cdna_length": 4341,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047448076.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.385A>G",
"hgvs_p": "p.Met129Val",
"transcript": "XM_047448077.1",
"protein_id": "XP_047304033.1",
"transcript_support_level": null,
"aa_start": 129,
"aa_end": null,
"aa_length": 916,
"cds_start": 385,
"cds_end": null,
"cds_length": 2751,
"cdna_start": 522,
"cdna_end": null,
"cdna_length": 4121,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047448077.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val",
"transcript": "XM_006710397.4",
"protein_id": "XP_006710460.1",
"transcript_support_level": null,
"aa_start": 166,
"aa_end": null,
"aa_length": 889,
"cds_start": 496,
"cds_end": null,
"cds_length": 2670,
"cdna_start": 633,
"cdna_end": null,
"cdna_length": 3097,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006710397.4"
},
{
"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": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "n.260A>G",
"hgvs_p": null,
"transcript": "ENST00000474241.1",
"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": 1036,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000474241.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"hgvs_c": "n.735A>G",
"hgvs_p": null,
"transcript": "XR_001737014.2",
"protein_id": null,
"transcript_support_level": null,
"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": 783,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_001737014.2"
}
],
"gene_symbol": "DPYD",
"gene_hgnc_id": 3012,
"dbsnp": "rs2297595",
"frequency_reference_population": 0.08950339,
"hom_count_reference_population": 7345,
"allele_count_reference_population": 144367,
"gnomad_exomes_af": 0.0904762,
"gnomad_genomes_af": 0.0801615,
"gnomad_exomes_ac": 132173,
"gnomad_genomes_ac": 12194,
"gnomad_exomes_homalt": 6719,
"gnomad_genomes_homalt": 626,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0019071698188781738,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.523,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.2209,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.21,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 7.559,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.03,
"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": "NM_000110.4",
"gene_symbol": "DPYD",
"hgnc_id": 3012,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.496A>G",
"hgvs_p": "p.Met166Val"
}
],
"clinvar_disease": "DPYD-related disorder,Dihydropyrimidine dehydrogenase deficiency,capecitabine response - Toxicity,fluorouracil response - Toxicity,not provided,not specified",
"clinvar_classification": "drug response",
"clinvar_review_status": "reviewed by expert panel",
"clinvar_submissions_summary": "US:1 LB:1 B:3 O:3",
"phenotype_combined": "not provided|Dihydropyrimidine dehydrogenase deficiency|not specified|DPYD-related disorder|capecitabine response - Toxicity|fluorouracil response - Toxicity",
"pathogenicity_classification_combined": "drug response",
"custom_annotations": null
}
],
"message": null
}