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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: 1-1051548-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=1051548&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 1051548,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000379370.7",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5466A>G",
"hgvs_p": "p.Ser1822Ser",
"transcript": "NM_198576.4",
"protein_id": "NP_940978.2",
"transcript_support_level": null,
"aa_start": 1822,
"aa_end": null,
"aa_length": 2045,
"cds_start": 5466,
"cds_end": null,
"cds_length": 6138,
"cdna_start": 5519,
"cdna_end": null,
"cdna_length": 7326,
"mane_select": "ENST00000379370.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5466A>G",
"hgvs_p": "p.Ser1822Ser",
"transcript": "ENST00000379370.7",
"protein_id": "ENSP00000368678.2",
"transcript_support_level": 1,
"aa_start": 1822,
"aa_end": null,
"aa_length": 2045,
"cds_start": 5466,
"cds_end": null,
"cds_length": 6138,
"cdna_start": 5519,
"cdna_end": null,
"cdna_length": 7326,
"mane_select": "NM_198576.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5478A>G",
"hgvs_p": "p.Ser1826Ser",
"transcript": "NM_001305275.2",
"protein_id": "NP_001292204.1",
"transcript_support_level": null,
"aa_start": 1826,
"aa_end": null,
"aa_length": 2068,
"cds_start": 5478,
"cds_end": null,
"cds_length": 6207,
"cdna_start": 5531,
"cdna_end": null,
"cdna_length": 7395,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5163A>G",
"hgvs_p": "p.Ser1721Ser",
"transcript": "ENST00000651234.1",
"protein_id": "ENSP00000499046.1",
"transcript_support_level": null,
"aa_start": 1721,
"aa_end": null,
"aa_length": 1963,
"cds_start": 5163,
"cds_end": null,
"cds_length": 5892,
"cdna_start": 5613,
"cdna_end": null,
"cdna_length": 7477,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5163A>G",
"hgvs_p": "p.Ser1721Ser",
"transcript": "NM_001364727.2",
"protein_id": "NP_001351656.1",
"transcript_support_level": null,
"aa_start": 1721,
"aa_end": null,
"aa_length": 1944,
"cds_start": 5163,
"cds_end": null,
"cds_length": 5835,
"cdna_start": 5726,
"cdna_end": null,
"cdna_length": 7533,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5151A>G",
"hgvs_p": "p.Ser1717Ser",
"transcript": "ENST00000652369.2",
"protein_id": "ENSP00000498543.1",
"transcript_support_level": null,
"aa_start": 1717,
"aa_end": null,
"aa_length": 1940,
"cds_start": 5151,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 5601,
"cdna_end": null,
"cdna_length": 7411,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5064A>G",
"hgvs_p": "p.Ser1688Ser",
"transcript": "ENST00000620552.4",
"protein_id": "ENSP00000484607.1",
"transcript_support_level": 5,
"aa_start": 1688,
"aa_end": null,
"aa_length": 1930,
"cds_start": 5064,
"cds_end": null,
"cds_length": 5793,
"cdna_start": 5528,
"cdna_end": null,
"cdna_length": 7394,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5478A>G",
"hgvs_p": "p.Ser1826Ser",
"transcript": "XM_005244749.4",
"protein_id": "XP_005244806.1",
"transcript_support_level": null,
"aa_start": 1826,
"aa_end": null,
"aa_length": 2049,
"cds_start": 5478,
"cds_end": null,
"cds_length": 6150,
"cdna_start": 5531,
"cdna_end": null,
"cdna_length": 7338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5478A>G",
"hgvs_p": "p.Ser1826Ser",
"transcript": "XM_011541429.3",
"protein_id": "XP_011539731.1",
"transcript_support_level": null,
"aa_start": 1826,
"aa_end": null,
"aa_length": 2004,
"cds_start": 5478,
"cds_end": null,
"cds_length": 6015,
"cdna_start": 5531,
"cdna_end": null,
"cdna_length": 6785,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.5466A>G",
"hgvs_p": "p.Ser1822Ser",
"transcript": "XM_047419836.1",
"protein_id": "XP_047275792.1",
"transcript_support_level": null,
"aa_start": 1822,
"aa_end": null,
"aa_length": 2000,
"cds_start": 5466,
"cds_end": null,
"cds_length": 6003,
"cdna_start": 5519,
"cdna_end": null,
"cdna_length": 6773,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.3744A>G",
"hgvs_p": "p.Ser1248Ser",
"transcript": "XM_047419837.1",
"protein_id": "XP_047275793.1",
"transcript_support_level": null,
"aa_start": 1248,
"aa_end": null,
"aa_length": 1471,
"cds_start": 3744,
"cds_end": null,
"cds_length": 4416,
"cdna_start": 4666,
"cdna_end": null,
"cdna_length": 6473,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"hgvs_c": "c.3744A>G",
"hgvs_p": "p.Ser1248Ser",
"transcript": "XM_047419838.1",
"protein_id": "XP_047275794.1",
"transcript_support_level": null,
"aa_start": 1248,
"aa_end": null,
"aa_length": 1471,
"cds_start": 3744,
"cds_end": null,
"cds_length": 4416,
"cdna_start": 4322,
"cdna_end": null,
"cdna_length": 6129,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "AGRN",
"gene_hgnc_id": 329,
"dbsnp": "rs149659540",
"frequency_reference_population": 0.00038516003,
"hom_count_reference_population": 1,
"allele_count_reference_population": 606,
"gnomad_exomes_af": 0.000196333,
"gnomad_genomes_af": 0.0021468,
"gnomad_exomes_ac": 279,
"gnomad_genomes_ac": 327,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.04899999871850014,
"computational_prediction_selected": "Benign",
"computational_source_selected": "REVEL",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.049,
"revel_prediction": "Benign",
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.55,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.044,
"phylop100way_prediction": "Benign",
"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": "Benign",
"acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BS1",
"acmg_by_gene": [
{
"score": -15,
"benign_score": 15,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Very_Strong",
"BP7",
"BS1"
],
"verdict": "Benign",
"transcript": "ENST00000379370.7",
"gene_symbol": "AGRN",
"hgnc_id": 329,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.5466A>G",
"hgvs_p": "p.Ser1822Ser"
}
],
"clinvar_disease": "Congenital myasthenic syndrome 8,not provided",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2 B:1",
"phenotype_combined": "Congenital myasthenic syndrome 8|not provided",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}