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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: X-50634194-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=50634194&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 50634194,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000376020.9",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "NM_020717.5",
"protein_id": "NP_065768.2",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 1493,
"cds_start": 1879,
"cds_end": null,
"cds_length": 4482,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 14557,
"mane_select": "ENST00000376020.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "ENST00000376020.9",
"protein_id": "ENSP00000365188.2",
"transcript_support_level": 2,
"aa_start": 627,
"aa_end": null,
"aa_length": 1493,
"cds_start": 1879,
"cds_end": null,
"cds_length": 4482,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 14557,
"mane_select": "NM_020717.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "ENST00000289292.11",
"protein_id": "ENSP00000289292.7",
"transcript_support_level": 1,
"aa_start": 627,
"aa_end": null,
"aa_length": 1493,
"cds_start": 1879,
"cds_end": null,
"cds_length": 4482,
"cdna_start": 2163,
"cdna_end": null,
"cdna_length": 6261,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1531C>T",
"hgvs_p": "p.Pro511Ser",
"transcript": "ENST00000460112.3",
"protein_id": "ENSP00000421450.1",
"transcript_support_level": 5,
"aa_start": 511,
"aa_end": null,
"aa_length": 1377,
"cds_start": 1531,
"cds_end": null,
"cds_length": 4134,
"cdna_start": 1986,
"cdna_end": null,
"cdna_length": 8919,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "XM_017029682.3",
"protein_id": "XP_016885171.1",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 1531,
"cds_start": 1879,
"cds_end": null,
"cds_length": 4596,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 14671,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1744C>T",
"hgvs_p": "p.Pro582Ser",
"transcript": "XM_017029683.2",
"protein_id": "XP_016885172.1",
"transcript_support_level": null,
"aa_start": 582,
"aa_end": null,
"aa_length": 1486,
"cds_start": 1744,
"cds_end": null,
"cds_length": 4461,
"cdna_start": 1920,
"cdna_end": null,
"cdna_length": 14536,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1744C>T",
"hgvs_p": "p.Pro582Ser",
"transcript": "XM_047442279.1",
"protein_id": "XP_047298235.1",
"transcript_support_level": null,
"aa_start": 582,
"aa_end": null,
"aa_length": 1448,
"cds_start": 1744,
"cds_end": null,
"cds_length": 4347,
"cdna_start": 1920,
"cdna_end": null,
"cdna_length": 14422,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1531C>T",
"hgvs_p": "p.Pro511Ser",
"transcript": "XM_017029684.2",
"protein_id": "XP_016885173.1",
"transcript_support_level": null,
"aa_start": 511,
"aa_end": null,
"aa_length": 1415,
"cds_start": 1531,
"cds_end": null,
"cds_length": 4248,
"cdna_start": 1975,
"cdna_end": null,
"cdna_length": 14591,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "XM_017029685.3",
"protein_id": "XP_016885174.1",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 1398,
"cds_start": 1879,
"cds_end": null,
"cds_length": 4197,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 4474,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser",
"transcript": "XM_017029687.3",
"protein_id": "XP_016885176.1",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 999,
"cds_start": 1879,
"cds_end": null,
"cds_length": 3000,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 3396,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "c.1744C>T",
"hgvs_p": "p.Pro582Ser",
"transcript": "XM_047442280.1",
"protein_id": "XP_047298236.1",
"transcript_support_level": null,
"aa_start": 582,
"aa_end": null,
"aa_length": 954,
"cds_start": 1744,
"cds_end": null,
"cds_length": 2865,
"cdna_start": 1920,
"cdna_end": null,
"cdna_length": 3261,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.2055C>T",
"hgvs_p": null,
"transcript": "NR_027121.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 11004,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.1920C>T",
"hgvs_p": null,
"transcript": "NR_172068.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10869,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.1975C>T",
"hgvs_p": null,
"transcript": "NR_172069.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10924,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.1840C>T",
"hgvs_p": null,
"transcript": "NR_172070.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10789,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.2055C>T",
"hgvs_p": null,
"transcript": "XR_001755716.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 11118,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.2055C>T",
"hgvs_p": null,
"transcript": "XR_001755717.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7563,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.2055C>T",
"hgvs_p": null,
"transcript": "XR_001755718.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7820,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.2055C>T",
"hgvs_p": null,
"transcript": "XR_007068196.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7706,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"hgvs_c": "n.1920C>T",
"hgvs_p": null,
"transcript": "XR_007068197.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7571,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SHROOM4",
"gene_hgnc_id": 29215,
"dbsnp": "rs150861758",
"frequency_reference_population": 0.002361031,
"hom_count_reference_population": 917,
"allele_count_reference_population": 2856,
"gnomad_exomes_af": 0.00245247,
"gnomad_genomes_af": 0.00146102,
"gnomad_exomes_ac": 2693,
"gnomad_genomes_ac": 163,
"gnomad_exomes_homalt": 5,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.007726848125457764,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.155,
"revel_prediction": "Benign",
"alphamissense_score": 0.0716,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.52,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.523,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS2",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000376020.9",
"gene_symbol": "SHROOM4",
"hgnc_id": 29215,
"effects": [
"missense_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "c.1879C>T",
"hgvs_p": "p.Pro627Ser"
}
],
"clinvar_disease": "History of neurodevelopmental disorder,not provided,not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3",
"phenotype_combined": "not specified|History of neurodevelopmental disorder|not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}