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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: 9-110800746-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=110800746&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 110800746,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000374448.9",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2368G>A",
"hgvs_p": "p.Val790Met",
"transcript": "NM_005592.4",
"protein_id": "NP_005583.1",
"transcript_support_level": null,
"aa_start": 790,
"aa_end": null,
"aa_length": 869,
"cds_start": 2368,
"cds_end": null,
"cds_length": 2610,
"cdna_start": 2482,
"cdna_end": null,
"cdna_length": 8294,
"mane_select": "ENST00000374448.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2368G>A",
"hgvs_p": "p.Val790Met",
"transcript": "ENST00000374448.9",
"protein_id": "ENSP00000363571.4",
"transcript_support_level": 5,
"aa_start": 790,
"aa_end": null,
"aa_length": 869,
"cds_start": 2368,
"cds_end": null,
"cds_length": 2610,
"cdna_start": 2482,
"cdna_end": null,
"cdna_length": 8294,
"mane_select": "NM_005592.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2344G>A",
"hgvs_p": "p.Val782Met",
"transcript": "ENST00000416899.7",
"protein_id": "ENSP00000393608.3",
"transcript_support_level": 5,
"aa_start": 782,
"aa_end": null,
"aa_length": 861,
"cds_start": 2344,
"cds_end": null,
"cds_length": 2586,
"cdna_start": 2470,
"cdna_end": null,
"cdna_length": 3344,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2110G>A",
"hgvs_p": "p.Val704Met",
"transcript": "NM_001166280.2",
"protein_id": "NP_001159752.1",
"transcript_support_level": null,
"aa_start": 704,
"aa_end": null,
"aa_length": 783,
"cds_start": 2110,
"cds_end": null,
"cds_length": 2352,
"cdna_start": 2224,
"cdna_end": null,
"cdna_length": 8036,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2110G>A",
"hgvs_p": "p.Val704Met",
"transcript": "ENST00000189978.10",
"protein_id": "ENSP00000189978.6",
"transcript_support_level": 5,
"aa_start": 704,
"aa_end": null,
"aa_length": 783,
"cds_start": 2110,
"cds_end": null,
"cds_length": 2352,
"cdna_start": 2156,
"cdna_end": null,
"cdna_length": 2408,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2080G>A",
"hgvs_p": "p.Val694Met",
"transcript": "NM_001166281.2",
"protein_id": "NP_001159753.1",
"transcript_support_level": null,
"aa_start": 694,
"aa_end": null,
"aa_length": 773,
"cds_start": 2080,
"cds_end": null,
"cds_length": 2322,
"cdna_start": 2194,
"cdna_end": null,
"cdna_length": 8006,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.1108G>A",
"hgvs_p": "p.Val370Met",
"transcript": "NM_001369398.1",
"protein_id": "NP_001356327.1",
"transcript_support_level": null,
"aa_start": 370,
"aa_end": null,
"aa_length": 449,
"cds_start": 1108,
"cds_end": null,
"cds_length": 1350,
"cdna_start": 1750,
"cdna_end": null,
"cdna_length": 7562,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2398G>A",
"hgvs_p": "p.Val800Met",
"transcript": "XM_005251994.4",
"protein_id": "XP_005252051.1",
"transcript_support_level": null,
"aa_start": 800,
"aa_end": null,
"aa_length": 879,
"cds_start": 2398,
"cds_end": null,
"cds_length": 2640,
"cdna_start": 2512,
"cdna_end": null,
"cdna_length": 8324,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2374G>A",
"hgvs_p": "p.Val792Met",
"transcript": "XM_005251995.4",
"protein_id": "XP_005252052.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 871,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2616,
"cdna_start": 2488,
"cdna_end": null,
"cdna_length": 8300,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2344G>A",
"hgvs_p": "p.Val782Met",
"transcript": "XM_005251996.4",
"protein_id": "XP_005252053.1",
"transcript_support_level": null,
"aa_start": 782,
"aa_end": null,
"aa_length": 861,
"cds_start": 2344,
"cds_end": null,
"cds_length": 2586,
"cdna_start": 2458,
"cdna_end": null,
"cdna_length": 8270,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.2134G>A",
"hgvs_p": "p.Val712Met",
"transcript": "XM_017014734.2",
"protein_id": "XP_016870223.1",
"transcript_support_level": null,
"aa_start": 712,
"aa_end": null,
"aa_length": 791,
"cds_start": 2134,
"cds_end": null,
"cds_length": 2376,
"cdna_start": 2248,
"cdna_end": null,
"cdna_length": 8060,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"hgvs_c": "c.1132G>A",
"hgvs_p": "p.Val378Met",
"transcript": "XM_011518708.3",
"protein_id": "XP_011517010.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 457,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 1247,
"cdna_end": null,
"cdna_length": 7059,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MUSK",
"gene_hgnc_id": 7525,
"dbsnp": "rs199476083",
"frequency_reference_population": 0.00012578398,
"hom_count_reference_population": 0,
"allele_count_reference_population": 203,
"gnomad_exomes_af": 0.000121775,
"gnomad_genomes_af": 0.000164294,
"gnomad_exomes_ac": 178,
"gnomad_genomes_ac": 25,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.6962610483169556,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.658,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.8253,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.21,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.998,
"phylop100way_prediction": "Pathogenic",
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM1,PP5,BS1_Supporting",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 1,
"pathogenic_score": 3,
"criteria": [
"PM1",
"PP5",
"BS1_Supporting"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000374448.9",
"gene_symbol": "MUSK",
"hgnc_id": 7525,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2368G>A",
"hgvs_p": "p.Val790Met"
}
],
"clinvar_disease": "Congenital myasthenic syndrome 9,Fetal akinesia deformation sequence 1,MUSK-related disorder,not provided",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "P:3 LP:3 US:2",
"phenotype_combined": "Congenital myasthenic syndrome 9|Fetal akinesia deformation sequence 1;Congenital myasthenic syndrome 9|not provided|MUSK-related disorder|Fetal akinesia deformation sequence 1",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}