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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: 2-206145009-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=206145009&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 206145009,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000233190.11",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.755A>G",
"hgvs_p": "p.Asp252Gly",
"transcript": "NM_005006.7",
"protein_id": "NP_004997.4",
"transcript_support_level": null,
"aa_start": 252,
"aa_end": null,
"aa_length": 727,
"cds_start": 755,
"cds_end": null,
"cds_length": 2184,
"cdna_start": 863,
"cdna_end": null,
"cdna_length": 11660,
"mane_select": "ENST00000233190.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.755A>G",
"hgvs_p": "p.Asp252Gly",
"transcript": "ENST00000233190.11",
"protein_id": "ENSP00000233190.5",
"transcript_support_level": 1,
"aa_start": 252,
"aa_end": null,
"aa_length": 727,
"cds_start": 755,
"cds_end": null,
"cds_length": 2184,
"cdna_start": 863,
"cdna_end": null,
"cdna_length": 11660,
"mane_select": "NM_005006.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.797A>G",
"hgvs_p": "p.Asp266Gly",
"transcript": "NM_001199984.2",
"protein_id": "NP_001186913.1",
"transcript_support_level": null,
"aa_start": 266,
"aa_end": null,
"aa_length": 741,
"cds_start": 797,
"cds_end": null,
"cds_length": 2226,
"cdna_start": 873,
"cdna_end": null,
"cdna_length": 11670,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.755A>G",
"hgvs_p": "p.Asp252Gly",
"transcript": "ENST00000449699.5",
"protein_id": "ENSP00000399912.1",
"transcript_support_level": 2,
"aa_start": 252,
"aa_end": null,
"aa_length": 727,
"cds_start": 755,
"cds_end": null,
"cds_length": 2184,
"cdna_start": 858,
"cdna_end": null,
"cdna_length": 2371,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.647A>G",
"hgvs_p": "p.Asp216Gly",
"transcript": "NM_001199981.2",
"protein_id": "NP_001186910.1",
"transcript_support_level": null,
"aa_start": 216,
"aa_end": null,
"aa_length": 691,
"cds_start": 647,
"cds_end": null,
"cds_length": 2076,
"cdna_start": 755,
"cdna_end": null,
"cdna_length": 11552,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.647A>G",
"hgvs_p": "p.Asp216Gly",
"transcript": "ENST00000440274.5",
"protein_id": "ENSP00000409766.1",
"transcript_support_level": 2,
"aa_start": 216,
"aa_end": null,
"aa_length": 691,
"cds_start": 647,
"cds_end": null,
"cds_length": 2076,
"cdna_start": 736,
"cdna_end": null,
"cdna_length": 2394,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.584A>G",
"hgvs_p": "p.Asp195Gly",
"transcript": "NM_001199983.2",
"protein_id": "NP_001186912.1",
"transcript_support_level": null,
"aa_start": 195,
"aa_end": null,
"aa_length": 670,
"cds_start": 584,
"cds_end": null,
"cds_length": 2013,
"cdna_start": 771,
"cdna_end": null,
"cdna_length": 11568,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.584A>G",
"hgvs_p": "p.Asp195Gly",
"transcript": "ENST00000423725.5",
"protein_id": "ENSP00000397760.1",
"transcript_support_level": 2,
"aa_start": 195,
"aa_end": null,
"aa_length": 670,
"cds_start": 584,
"cds_end": null,
"cds_length": 2013,
"cdna_start": 836,
"cdna_end": null,
"cdna_length": 2631,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.422A>G",
"hgvs_p": "p.Asp141Gly",
"transcript": "NM_001199982.2",
"protein_id": "NP_001186911.1",
"transcript_support_level": null,
"aa_start": 141,
"aa_end": null,
"aa_length": 616,
"cds_start": 422,
"cds_end": null,
"cds_length": 1851,
"cdna_start": 586,
"cdna_end": null,
"cdna_length": 11383,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.422A>G",
"hgvs_p": "p.Asp141Gly",
"transcript": "ENST00000432169.5",
"protein_id": "ENSP00000409689.1",
"transcript_support_level": 2,
"aa_start": 141,
"aa_end": null,
"aa_length": 616,
"cds_start": 422,
"cds_end": null,
"cds_length": 1851,
"cdna_start": 567,
"cdna_end": null,
"cdna_length": 2080,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"hgvs_c": "c.407A>G",
"hgvs_p": "p.Asp136Gly",
"transcript": "ENST00000457011.5",
"protein_id": "ENSP00000400976.1",
"transcript_support_level": 2,
"aa_start": 136,
"aa_end": null,
"aa_length": 611,
"cds_start": 407,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 502,
"cdna_end": null,
"cdna_length": 2171,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "NDUFS1",
"gene_hgnc_id": 7707,
"dbsnp": "rs199422224",
"frequency_reference_population": 0.000007436262,
"hom_count_reference_population": 0,
"allele_count_reference_population": 12,
"gnomad_exomes_af": 0.00000752651,
"gnomad_genomes_af": 0.0000065697,
"gnomad_exomes_ac": 11,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9716318845748901,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.941,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9172,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.44,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.889,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.05,
"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": 15,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PM2,PP2,PP3_Strong,PP5_Very_Strong",
"acmg_by_gene": [
{
"score": 15,
"benign_score": 0,
"pathogenic_score": 15,
"criteria": [
"PM2",
"PP2",
"PP3_Strong",
"PP5_Very_Strong"
],
"verdict": "Pathogenic",
"transcript": "ENST00000233190.11",
"gene_symbol": "NDUFS1",
"hgnc_id": 7707,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.755A>G",
"hgvs_p": "p.Asp252Gly"
}
],
"clinvar_disease": " nuclear type 5,Mitochondrial complex I deficiency,not provided",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:2",
"phenotype_combined": "Mitochondrial complex I deficiency, nuclear type 5|not provided",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}