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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: 19-50268175-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=50268175&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 50268175,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "ENST00000642316.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2841C>T",
"hgvs_p": "p.Arg947Arg",
"transcript": "NM_001145809.2",
"protein_id": "NP_001139281.1",
"transcript_support_level": null,
"aa_start": 947,
"aa_end": null,
"aa_length": 2036,
"cds_start": 2841,
"cds_end": null,
"cds_length": 6111,
"cdna_start": 2894,
"cdna_end": null,
"cdna_length": 6914,
"mane_select": "ENST00000642316.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2841C>T",
"hgvs_p": "p.Arg947Arg",
"transcript": "ENST00000642316.2",
"protein_id": "ENSP00000493594.1",
"transcript_support_level": null,
"aa_start": 947,
"aa_end": null,
"aa_length": 2036,
"cds_start": 2841,
"cds_end": null,
"cds_length": 6111,
"cdna_start": 2894,
"cdna_end": null,
"cdna_length": 6914,
"mane_select": "NM_001145809.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2742C>T",
"hgvs_p": "p.Arg914Arg",
"transcript": "ENST00000599920.5",
"protein_id": "ENSP00000469573.1",
"transcript_support_level": 1,
"aa_start": 914,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2742,
"cds_end": null,
"cds_length": 3008,
"cdna_start": 2780,
"cdna_end": null,
"cdna_length": 3046,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2742C>T",
"hgvs_p": "p.Arg914Arg",
"transcript": "NM_001077186.2",
"protein_id": "NP_001070654.1",
"transcript_support_level": null,
"aa_start": 914,
"aa_end": null,
"aa_length": 2003,
"cds_start": 2742,
"cds_end": null,
"cds_length": 6012,
"cdna_start": 2795,
"cdna_end": null,
"cdna_length": 6815,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2742C>T",
"hgvs_p": "p.Arg914Arg",
"transcript": "ENST00000425460.6",
"protein_id": "ENSP00000407879.1",
"transcript_support_level": 5,
"aa_start": 914,
"aa_end": null,
"aa_length": 2003,
"cds_start": 2742,
"cds_end": null,
"cds_length": 6012,
"cdna_start": 2795,
"cdna_end": null,
"cdna_length": 6815,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2742C>T",
"hgvs_p": "p.Arg914Arg",
"transcript": "ENST00000598205.5",
"protein_id": "ENSP00000472543.1",
"transcript_support_level": 5,
"aa_start": 914,
"aa_end": null,
"aa_length": 2003,
"cds_start": 2742,
"cds_end": null,
"cds_length": 6012,
"cdna_start": 2867,
"cdna_end": null,
"cdna_length": 6137,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2718C>T",
"hgvs_p": "p.Arg906Arg",
"transcript": "NM_024729.4",
"protein_id": "NP_079005.3",
"transcript_support_level": null,
"aa_start": 906,
"aa_end": null,
"aa_length": 1995,
"cds_start": 2718,
"cds_end": null,
"cds_length": 5988,
"cdna_start": 2771,
"cdna_end": null,
"cdna_length": 6791,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2718C>T",
"hgvs_p": "p.Arg906Arg",
"transcript": "ENST00000376970.6",
"protein_id": "ENSP00000366169.3",
"transcript_support_level": 5,
"aa_start": 906,
"aa_end": null,
"aa_length": 1995,
"cds_start": 2718,
"cds_end": null,
"cds_length": 5988,
"cdna_start": 2765,
"cdna_end": null,
"cdna_length": 6787,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"hgvs_c": "c.2718C>T",
"hgvs_p": "p.Arg906Arg",
"transcript": "ENST00000596571.5",
"protein_id": "ENSP00000472819.1",
"transcript_support_level": 5,
"aa_start": 906,
"aa_end": null,
"aa_length": 1995,
"cds_start": 2718,
"cds_end": null,
"cds_length": 5988,
"cdna_start": 2718,
"cdna_end": null,
"cdna_length": 5988,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MYH14",
"gene_hgnc_id": 23212,
"dbsnp": "rs138987081",
"frequency_reference_population": 0.013665342,
"hom_count_reference_population": 183,
"allele_count_reference_population": 21144,
"gnomad_exomes_af": 0.0140408,
"gnomad_genomes_af": 0.0102271,
"gnomad_exomes_ac": 19586,
"gnomad_genomes_ac": 1558,
"gnomad_exomes_homalt": 169,
"gnomad_genomes_homalt": 14,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.550000011920929,
"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": -0.55,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.717,
"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": -21,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
"acmg_by_gene": [
{
"score": -21,
"benign_score": 21,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000642316.2",
"gene_symbol": "MYH14",
"hgnc_id": 23212,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.2841C>T",
"hgvs_p": "p.Arg947Arg"
}
],
"clinvar_disease": "Autosomal dominant nonsyndromic hearing loss 4A,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:9",
"phenotype_combined": "not specified|Autosomal dominant nonsyndromic hearing loss 4A|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}