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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: 5-16670764-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=16670764&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 16670764,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_012334.3",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 39,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.5645C>T",
"hgvs_p": "p.Thr1882Met",
"transcript": "NM_012334.3",
"protein_id": "NP_036466.2",
"transcript_support_level": null,
"aa_start": 1882,
"aa_end": null,
"aa_length": 2058,
"cds_start": 5645,
"cds_end": null,
"cds_length": 6177,
"cdna_start": 6125,
"cdna_end": null,
"cdna_length": 11442,
"mane_select": "ENST00000513610.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012334.3"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 39,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.5645C>T",
"hgvs_p": "p.Thr1882Met",
"transcript": "ENST00000513610.6",
"protein_id": "ENSP00000421280.1",
"transcript_support_level": 1,
"aa_start": 1882,
"aa_end": null,
"aa_length": 2058,
"cds_start": 5645,
"cds_end": null,
"cds_length": 6177,
"cdna_start": 6125,
"cdna_end": null,
"cdna_length": 11442,
"mane_select": "NM_012334.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000513610.6"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 39,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.5678C>T",
"hgvs_p": "p.Thr1893Met",
"transcript": "ENST00000274203.13",
"protein_id": "ENSP00000274203.10",
"transcript_support_level": 5,
"aa_start": 1893,
"aa_end": null,
"aa_length": 2069,
"cds_start": 5678,
"cds_end": null,
"cds_length": 6210,
"cdna_start": 6146,
"cdna_end": null,
"cdna_length": 11456,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000274203.13"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.3662C>T",
"hgvs_p": "p.Thr1221Met",
"transcript": "ENST00000505695.5",
"protein_id": "ENSP00000421170.1",
"transcript_support_level": 2,
"aa_start": 1221,
"aa_end": null,
"aa_length": 1397,
"cds_start": 3662,
"cds_end": null,
"cds_length": 4194,
"cdna_start": 4141,
"cdna_end": null,
"cdna_length": 4803,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000505695.5"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.3662C>T",
"hgvs_p": "p.Thr1221Met",
"transcript": "ENST00000515803.5",
"protein_id": "ENSP00000425051.1",
"transcript_support_level": 2,
"aa_start": 1221,
"aa_end": null,
"aa_length": 1397,
"cds_start": 3662,
"cds_end": null,
"cds_length": 4194,
"cdna_start": 3995,
"cdna_end": null,
"cdna_length": 4839,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000515803.5"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 38,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.5576C>T",
"hgvs_p": "p.Thr1859Met",
"transcript": "XM_006714475.4",
"protein_id": "XP_006714538.1",
"transcript_support_level": null,
"aa_start": 1859,
"aa_end": null,
"aa_length": 2035,
"cds_start": 5576,
"cds_end": null,
"cds_length": 6108,
"cdna_start": 6056,
"cdna_end": null,
"cdna_length": 11373,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006714475.4"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.3719C>T",
"hgvs_p": "p.Thr1240Met",
"transcript": "XM_005248306.5",
"protein_id": "XP_005248363.1",
"transcript_support_level": null,
"aa_start": 1240,
"aa_end": null,
"aa_length": 1416,
"cds_start": 3719,
"cds_end": null,
"cds_length": 4251,
"cdna_start": 3832,
"cdna_end": null,
"cdna_length": 9149,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005248306.5"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.3716C>T",
"hgvs_p": "p.Thr1239Met",
"transcript": "XM_005248307.3",
"protein_id": "XP_005248364.1",
"transcript_support_level": null,
"aa_start": 1239,
"aa_end": null,
"aa_length": 1415,
"cds_start": 3716,
"cds_end": null,
"cds_length": 4248,
"cdna_start": 3822,
"cdna_end": null,
"cdna_length": 9139,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005248307.3"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"hgvs_c": "c.3716C>T",
"hgvs_p": "p.Thr1239Met",
"transcript": "XM_011514046.3",
"protein_id": "XP_011512348.1",
"transcript_support_level": null,
"aa_start": 1239,
"aa_end": null,
"aa_length": 1415,
"cds_start": 3716,
"cds_end": null,
"cds_length": 4248,
"cdna_start": 3769,
"cdna_end": null,
"cdna_length": 9086,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011514046.3"
},
{
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "RETREG1-AS1",
"gene_hgnc_id": 55551,
"hgvs_c": "n.330-8070G>A",
"hgvs_p": null,
"transcript": "ENST00000653650.1",
"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": 1894,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000653650.1"
}
],
"gene_symbol": "MYO10",
"gene_hgnc_id": 7593,
"dbsnp": "rs532130077",
"frequency_reference_population": 0.000011771936,
"hom_count_reference_population": 0,
"allele_count_reference_population": 19,
"gnomad_exomes_af": 0.00000957782,
"gnomad_genomes_af": 0.0000328304,
"gnomad_exomes_ac": 14,
"gnomad_genomes_ac": 5,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3163427412509918,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.477,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.1543,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.11,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 6.448,
"phylop100way_prediction": "Uncertain_significance",
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_012334.3",
"gene_symbol": "MYO10",
"hgnc_id": 7593,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.5645C>T",
"hgvs_p": "p.Thr1882Met"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000653650.1",
"gene_symbol": "RETREG1-AS1",
"hgnc_id": 55551,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.330-8070G>A",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}