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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: 9-110800319-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=110800319&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 8,
"criteria": [
"BP4_Moderate",
"BP6",
"BP7",
"BS1"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "MUSK",
"hgnc_id": 7525,
"hgvs_c": "c.1941C>T",
"hgvs_p": "p.Val647Val",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -8,
"transcript": "NM_005592.4",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Moderate,BP6,BP7,BS1",
"acmg_score": -8,
"allele_count_reference_population": 306,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.41,
"chr": "9",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": "Congenital myasthenic syndrome 9,Fetal akinesia deformation sequence 1,not specified",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:1 LB:1 B:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.4099999964237213,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 869,
"aa_ref": "V",
"aa_start": 647,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8294,
"cdna_start": 2055,
"cds_end": null,
"cds_length": 2610,
"cds_start": 1941,
"consequences": [
"synonymous_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "NM_005592.4",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1941C>T",
"hgvs_p": "p.Val647Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000374448.9",
"protein_coding": true,
"protein_id": "NP_005583.1",
"strand": true,
"transcript": "NM_005592.4",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 869,
"aa_ref": "V",
"aa_start": 647,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 8294,
"cdna_start": 2055,
"cds_end": null,
"cds_length": 2610,
"cds_start": 1941,
"consequences": [
"synonymous_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000374448.9",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1941C>T",
"hgvs_p": "p.Val647Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_005592.4",
"protein_coding": true,
"protein_id": "ENSP00000363571.4",
"strand": true,
"transcript": "ENST00000374448.9",
"transcript_support_level": 5
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 861,
"aa_ref": "V",
"aa_start": 639,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3344,
"cdna_start": 2043,
"cds_end": null,
"cds_length": 2586,
"cds_start": 1917,
"consequences": [
"synonymous_variant"
],
"exon_count": 14,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000416899.7",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1917C>T",
"hgvs_p": "p.Val639Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000393608.3",
"strand": true,
"transcript": "ENST00000416899.7",
"transcript_support_level": 5
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 783,
"aa_ref": "V",
"aa_start": 561,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8036,
"cdna_start": 1797,
"cds_end": null,
"cds_length": 2352,
"cds_start": 1683,
"consequences": [
"synonymous_variant"
],
"exon_count": 14,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "NM_001166280.2",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1683C>T",
"hgvs_p": "p.Val561Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001159752.1",
"strand": true,
"transcript": "NM_001166280.2",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 783,
"aa_ref": "V",
"aa_start": 561,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2408,
"cdna_start": 1729,
"cds_end": null,
"cds_length": 2352,
"cds_start": 1683,
"consequences": [
"synonymous_variant"
],
"exon_count": 14,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000189978.10",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1683C>T",
"hgvs_p": "p.Val561Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000189978.6",
"strand": true,
"transcript": "ENST00000189978.10",
"transcript_support_level": 5
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 773,
"aa_ref": "V",
"aa_start": 551,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8006,
"cdna_start": 1767,
"cds_end": null,
"cds_length": 2322,
"cds_start": 1653,
"consequences": [
"synonymous_variant"
],
"exon_count": 13,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001166281.2",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1653C>T",
"hgvs_p": "p.Val551Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001159753.1",
"strand": true,
"transcript": "NM_001166281.2",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 449,
"aa_ref": "V",
"aa_start": 227,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7562,
"cdna_start": 1323,
"cds_end": null,
"cds_length": 1350,
"cds_start": 681,
"consequences": [
"synonymous_variant"
],
"exon_count": 10,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001369398.1",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.681C>T",
"hgvs_p": "p.Val227Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001356327.1",
"strand": true,
"transcript": "NM_001369398.1",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 879,
"aa_ref": "V",
"aa_start": 657,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8324,
"cdna_start": 2085,
"cds_end": null,
"cds_length": 2640,
"cds_start": 1971,
"consequences": [
"synonymous_variant"
],
"exon_count": 16,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "XM_005251994.4",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1971C>T",
"hgvs_p": "p.Val657Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005252051.1",
"strand": true,
"transcript": "XM_005251994.4",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 871,
"aa_ref": "V",
"aa_start": 649,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8300,
"cdna_start": 2061,
"cds_end": null,
"cds_length": 2616,
"cds_start": 1947,
"consequences": [
"synonymous_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "XM_005251995.4",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1947C>T",
"hgvs_p": "p.Val649Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005252052.1",
"strand": true,
"transcript": "XM_005251995.4",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 861,
"aa_ref": "V",
"aa_start": 639,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8270,
"cdna_start": 2031,
"cds_end": null,
"cds_length": 2586,
"cds_start": 1917,
"consequences": [
"synonymous_variant"
],
"exon_count": 14,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "XM_005251996.4",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1917C>T",
"hgvs_p": "p.Val639Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005252053.1",
"strand": true,
"transcript": "XM_005251996.4",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 791,
"aa_ref": "V",
"aa_start": 569,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8060,
"cdna_start": 1821,
"cds_end": null,
"cds_length": 2376,
"cds_start": 1707,
"consequences": [
"synonymous_variant"
],
"exon_count": 15,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "XM_017014734.2",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.1707C>T",
"hgvs_p": "p.Val569Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016870223.1",
"strand": true,
"transcript": "XM_017014734.2",
"transcript_support_level": null
},
{
"aa_alt": "V",
"aa_end": null,
"aa_length": 457,
"aa_ref": "V",
"aa_start": 235,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7059,
"cdna_start": 820,
"cds_end": null,
"cds_length": 1374,
"cds_start": 705,
"consequences": [
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "XM_011518708.3",
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"hgvs_c": "c.705C>T",
"hgvs_p": "p.Val235Val",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011517010.1",
"strand": true,
"transcript": "XM_011518708.3",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs200312379",
"effect": "synonymous_variant",
"frequency_reference_population": 0.00019033851,
"gene_hgnc_id": 7525,
"gene_symbol": "MUSK",
"gnomad_exomes_ac": 152,
"gnomad_exomes_af": 0.000104425,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_ac": 154,
"gnomad_genomes_af": 0.00101269,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"phenotype_combined": "not specified|Congenital myasthenic syndrome 9|Congenital myasthenic syndrome 9;Fetal akinesia deformation sequence 1",
"phylop100way_prediction": "Benign",
"phylop100way_score": -1.037,
"pos": 110800319,
"ref": "C",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0.019999999552965164,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0.02,
"transcript": "NM_005592.4"
}
]
}