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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: 17-31343104-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=31343104&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 31343104,
"ref": "T",
"alt": "C",
"effect": "synonymous_variant",
"transcript": "NM_001042492.3",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7158T>C",
"hgvs_p": "p.Phe2386Phe",
"transcript": "NM_001042492.3",
"protein_id": "NP_001035957.1",
"transcript_support_level": null,
"aa_start": 2386,
"aa_end": null,
"aa_length": 2839,
"cds_start": 7158,
"cds_end": null,
"cds_length": 8520,
"cdna_start": 7491,
"cdna_end": null,
"cdna_length": 12373,
"mane_select": "ENST00000358273.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001042492.3"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7158T>C",
"hgvs_p": "p.Phe2386Phe",
"transcript": "ENST00000358273.9",
"protein_id": "ENSP00000351015.4",
"transcript_support_level": 1,
"aa_start": 2386,
"aa_end": null,
"aa_length": 2839,
"cds_start": 7158,
"cds_end": null,
"cds_length": 8520,
"cdna_start": 7491,
"cdna_end": null,
"cdna_length": 12373,
"mane_select": "NM_001042492.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000358273.9"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 47,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7095T>C",
"hgvs_p": "p.Phe2365Phe",
"transcript": "ENST00000356175.7",
"protein_id": "ENSP00000348498.3",
"transcript_support_level": 1,
"aa_start": 2365,
"aa_end": null,
"aa_length": 2818,
"cds_start": 7095,
"cds_end": null,
"cds_length": 8457,
"cdna_start": 7478,
"cdna_end": null,
"cdna_length": 12362,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000356175.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.*2323T>C",
"hgvs_p": null,
"transcript": "ENST00000579081.6",
"protein_id": "ENSP00000462408.2",
"transcript_support_level": 1,
"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": 8788,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000579081.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.*2323T>C",
"hgvs_p": null,
"transcript": "ENST00000579081.6",
"protein_id": "ENSP00000462408.2",
"transcript_support_level": 1,
"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": 8788,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000579081.6"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 49,
"exon_rank_end": null,
"exon_count": 59,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7188T>C",
"hgvs_p": "p.Phe2396Phe",
"transcript": "ENST00000691014.1",
"protein_id": "ENSP00000510595.1",
"transcript_support_level": null,
"aa_start": 2396,
"aa_end": null,
"aa_length": 2849,
"cds_start": 7188,
"cds_end": null,
"cds_length": 8550,
"cdna_start": 7521,
"cdna_end": null,
"cdna_length": 12415,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000691014.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 47,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7095T>C",
"hgvs_p": "p.Phe2365Phe",
"transcript": "NM_000267.4",
"protein_id": "NP_000258.1",
"transcript_support_level": null,
"aa_start": 2365,
"aa_end": null,
"aa_length": 2818,
"cds_start": 7095,
"cds_end": null,
"cds_length": 8457,
"cdna_start": 7428,
"cdna_end": null,
"cdna_length": 12310,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000267.4"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 48,
"exon_rank_end": null,
"exon_count": 59,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.7140T>C",
"hgvs_p": "p.Phe2380Phe",
"transcript": "ENST00000696138.1",
"protein_id": "ENSP00000512431.1",
"transcript_support_level": null,
"aa_start": 2380,
"aa_end": null,
"aa_length": 2807,
"cds_start": 7140,
"cds_end": null,
"cds_length": 8424,
"cdna_start": 7523,
"cdna_end": null,
"cdna_length": 12484,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000696138.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 39,
"exon_rank_end": null,
"exon_count": 50,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.6093T>C",
"hgvs_p": "p.Phe2031Phe",
"transcript": "ENST00000456735.6",
"protein_id": "ENSP00000389907.2",
"transcript_support_level": 5,
"aa_start": 2031,
"aa_end": null,
"aa_length": 2502,
"cds_start": 6093,
"cds_end": null,
"cds_length": 7509,
"cdna_start": 6093,
"cdna_end": null,
"cdna_length": 7787,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000456735.6"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.1722T>C",
"hgvs_p": "p.Phe574Phe",
"transcript": "ENST00000684826.1",
"protein_id": "ENSP00000509994.1",
"transcript_support_level": null,
"aa_start": 574,
"aa_end": null,
"aa_length": 1045,
"cds_start": 1722,
"cds_end": null,
"cds_length": 3138,
"cdna_start": 2431,
"cdna_end": null,
"cdna_length": 7344,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000684826.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.1722T>C",
"hgvs_p": "p.Phe574Phe",
"transcript": "ENST00000693617.1",
"protein_id": "ENSP00000510031.1",
"transcript_support_level": null,
"aa_start": 574,
"aa_end": null,
"aa_length": 1027,
"cds_start": 1722,
"cds_end": null,
"cds_length": 3084,
"cdna_start": 2607,
"cdna_end": null,
"cdna_length": 7501,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000693617.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.1314T>C",
"hgvs_p": "p.Phe438Phe",
"transcript": "ENST00000687027.1",
"protein_id": "ENSP00000508715.1",
"transcript_support_level": null,
"aa_start": 438,
"aa_end": null,
"aa_length": 891,
"cds_start": 1314,
"cds_end": null,
"cds_length": 2676,
"cdna_start": 2091,
"cdna_end": null,
"cdna_length": 6985,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000687027.1"
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "c.96T>C",
"hgvs_p": "p.Phe32Phe",
"transcript": "ENST00000689464.1",
"protein_id": "ENSP00000510673.1",
"transcript_support_level": null,
"aa_start": 32,
"aa_end": null,
"aa_length": 540,
"cds_start": 96,
"cds_end": null,
"cds_length": 1623,
"cdna_start": 97,
"cdna_end": null,
"cdna_length": 5082,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000689464.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.540T>C",
"hgvs_p": null,
"transcript": "ENST00000471572.6",
"protein_id": "ENSP00000464678.1",
"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": 2028,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000471572.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.300T>C",
"hgvs_p": null,
"transcript": "ENST00000581790.5",
"protein_id": "ENSP00000462700.1",
"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": 1256,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000581790.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.400T>C",
"hgvs_p": null,
"transcript": "ENST00000582892.1",
"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": 462,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000582892.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.3803T>C",
"hgvs_p": null,
"transcript": "ENST00000687863.1",
"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": 5018,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000687863.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"hgvs_c": "n.*6T>C",
"hgvs_p": null,
"transcript": "ENST00000584328.1",
"protein_id": null,
"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": 566,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000584328.1"
}
],
"gene_symbol": "NF1",
"gene_hgnc_id": 7765,
"dbsnp": "rs876660271",
"frequency_reference_population": 0.0000041050343,
"hom_count_reference_population": 0,
"allele_count_reference_population": 6,
"gnomad_exomes_af": 0.00000410503,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 6,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.5,
"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": -0.5,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.136,
"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": -14,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2_Supporting",
"acmg_by_gene": [
{
"score": -14,
"benign_score": 14,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS2_Supporting"
],
"verdict": "Benign",
"transcript": "NM_001042492.3",
"gene_symbol": "NF1",
"hgnc_id": 7765,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.7158T>C",
"hgvs_p": "p.Phe2386Phe"
}
],
"clinvar_disease": " type 1,Hereditary cancer-predisposing syndrome,Neurofibromatosis,not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:4",
"phenotype_combined": "Hereditary cancer-predisposing syndrome|Neurofibromatosis, type 1|not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}