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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: 5-148402010-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=148402010&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 148402010,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000340253.10",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "NM_205836.3",
"protein_id": "NP_995308.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 1188,
"cds_start": 291,
"cds_end": null,
"cds_length": 3567,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 4401,
"mane_select": "ENST00000340253.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "ENST00000340253.10",
"protein_id": "ENSP00000342023.6",
"transcript_support_level": 5,
"aa_start": 97,
"aa_end": null,
"aa_length": 1188,
"cds_start": 291,
"cds_end": null,
"cds_length": 3567,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 4401,
"mane_select": "NM_205836.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "ENST00000394370.7",
"protein_id": "ENSP00000377895.3",
"transcript_support_level": 1,
"aa_start": 97,
"aa_end": null,
"aa_length": 1113,
"cds_start": 291,
"cds_end": null,
"cds_length": 3342,
"cdna_start": 392,
"cdna_end": null,
"cdna_length": 4132,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "ENST00000513826.1",
"protein_id": "ENSP00000426410.1",
"transcript_support_level": 1,
"aa_start": 97,
"aa_end": null,
"aa_length": 943,
"cds_start": 291,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 356,
"cdna_end": null,
"cdna_length": 3585,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "NM_030793.5",
"protein_id": "NP_110420.3",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 1113,
"cds_start": 291,
"cds_end": null,
"cds_length": 3342,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 4176,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "NM_001271723.2",
"protein_id": "NP_001258652.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 943,
"cds_start": 291,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 3666,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "ENST00000296701.10",
"protein_id": "ENSP00000296701.6",
"transcript_support_level": 2,
"aa_start": 97,
"aa_end": null,
"aa_length": 943,
"cds_start": 291,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 459,
"cdna_end": null,
"cdna_length": 3680,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_024446223.2",
"protein_id": "XP_024301991.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 1188,
"cds_start": 291,
"cds_end": null,
"cds_length": 3567,
"cdna_start": 1503,
"cdna_end": null,
"cdna_length": 5468,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_006714797.3",
"protein_id": "XP_006714860.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 1146,
"cds_start": 291,
"cds_end": null,
"cds_length": 3441,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 4275,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_047417784.1",
"protein_id": "XP_047273740.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 1113,
"cds_start": 291,
"cds_end": null,
"cds_length": 3342,
"cdna_start": 1503,
"cdna_end": null,
"cdna_length": 5243,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_047417785.1",
"protein_id": "XP_047273741.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 994,
"cds_start": 291,
"cds_end": null,
"cds_length": 2985,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 3229,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_047417786.1",
"protein_id": "XP_047273742.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 943,
"cds_start": 291,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 1503,
"cdna_end": null,
"cdna_length": 4733,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu",
"transcript": "XM_047417789.1",
"protein_id": "XP_047273745.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 749,
"cds_start": 291,
"cds_end": null,
"cds_length": 2250,
"cdna_start": 436,
"cdna_end": null,
"cdna_length": 2494,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.165A>G",
"hgvs_p": null,
"transcript": "ENST00000502629.1",
"protein_id": null,
"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": 386,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.500A>G",
"hgvs_p": null,
"transcript": "ENST00000503613.5",
"protein_id": null,
"transcript_support_level": 3,
"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": 627,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.392A>G",
"hgvs_p": null,
"transcript": "ENST00000508326.5",
"protein_id": null,
"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": 745,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.356A>G",
"hgvs_p": null,
"transcript": "ENST00000509699.6",
"protein_id": null,
"transcript_support_level": 3,
"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": 1030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.340A>G",
"hgvs_p": null,
"transcript": "ENST00000521160.5",
"protein_id": null,
"transcript_support_level": 4,
"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": 590,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"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": "FBXO38",
"gene_hgnc_id": 28844,
"hgvs_c": "n.221+7106A>G",
"hgvs_p": null,
"transcript": "ENST00000511080.5",
"protein_id": null,
"transcript_support_level": 4,
"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": 514,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "FBXO38",
"gene_hgnc_id": 28844,
"dbsnp": "rs1339219934",
"frequency_reference_population": 0.00000434038,
"hom_count_reference_population": 0,
"allele_count_reference_population": 7,
"gnomad_exomes_af": 0.00000410785,
"gnomad_genomes_af": 0.00000657272,
"gnomad_exomes_ac": 6,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.5699999928474426,
"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": -0.57,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.374,
"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": -11,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Moderate,BP7,BS2",
"acmg_by_gene": [
{
"score": -11,
"benign_score": 11,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000340253.10",
"gene_symbol": "FBXO38",
"hgnc_id": 28844,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.291A>G",
"hgvs_p": "p.Leu97Leu"
}
],
"clinvar_disease": "Distal hereditary motor neuropathy type 2",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "Distal hereditary motor neuropathy type 2",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}