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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: 22-40827202-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=40827202&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 40827202,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_003932.5",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.875A>G",
"hgvs_p": "p.Asn292Ser",
"transcript": "NM_003932.5",
"protein_id": "NP_003923.2",
"transcript_support_level": null,
"aa_start": 292,
"aa_end": null,
"aa_length": 369,
"cds_start": 875,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000216218.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003932.5"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.875A>G",
"hgvs_p": "p.Asn292Ser",
"transcript": "ENST00000216218.8",
"protein_id": "ENSP00000216218.3",
"transcript_support_level": 1,
"aa_start": 292,
"aa_end": null,
"aa_length": 369,
"cds_start": 875,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003932.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000216218.8"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.992A>G",
"hgvs_p": "p.Asn331Ser",
"transcript": "ENST00000893870.1",
"protein_id": "ENSP00000563929.1",
"transcript_support_level": null,
"aa_start": 331,
"aa_end": null,
"aa_length": 408,
"cds_start": 992,
"cds_end": null,
"cds_length": 1227,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893870.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "ENST00000893867.1",
"protein_id": "ENSP00000563926.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 394,
"cds_start": 950,
"cds_end": null,
"cds_length": 1185,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893867.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.929A>G",
"hgvs_p": "p.Asn310Ser",
"transcript": "ENST00000960885.1",
"protein_id": "ENSP00000630944.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 387,
"cds_start": 929,
"cds_end": null,
"cds_length": 1164,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960885.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.905A>G",
"hgvs_p": "p.Asn302Ser",
"transcript": "ENST00000893864.1",
"protein_id": "ENSP00000563923.1",
"transcript_support_level": null,
"aa_start": 302,
"aa_end": null,
"aa_length": 379,
"cds_start": 905,
"cds_end": null,
"cds_length": 1140,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893864.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.872A>G",
"hgvs_p": "p.Asn291Ser",
"transcript": "ENST00000893862.1",
"protein_id": "ENSP00000563921.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 368,
"cds_start": 872,
"cds_end": null,
"cds_length": 1107,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893862.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.860A>G",
"hgvs_p": "p.Asn287Ser",
"transcript": "ENST00000893865.1",
"protein_id": "ENSP00000563924.1",
"transcript_support_level": null,
"aa_start": 287,
"aa_end": null,
"aa_length": 364,
"cds_start": 860,
"cds_end": null,
"cds_length": 1095,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893865.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.845A>G",
"hgvs_p": "p.Asn282Ser",
"transcript": "NM_001278589.2",
"protein_id": "NP_001265518.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 359,
"cds_start": 845,
"cds_end": null,
"cds_length": 1080,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278589.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.845A>G",
"hgvs_p": "p.Asn282Ser",
"transcript": "ENST00000893871.1",
"protein_id": "ENSP00000563930.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 359,
"cds_start": 845,
"cds_end": null,
"cds_length": 1080,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893871.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.836A>G",
"hgvs_p": "p.Asn279Ser",
"transcript": "ENST00000893863.1",
"protein_id": "ENSP00000563922.1",
"transcript_support_level": null,
"aa_start": 279,
"aa_end": null,
"aa_length": 356,
"cds_start": 836,
"cds_end": null,
"cds_length": 1071,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893863.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.758A>G",
"hgvs_p": "p.Asn253Ser",
"transcript": "ENST00000893868.1",
"protein_id": "ENSP00000563927.1",
"transcript_support_level": null,
"aa_start": 253,
"aa_end": null,
"aa_length": 330,
"cds_start": 758,
"cds_end": null,
"cds_length": 993,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893868.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.728A>G",
"hgvs_p": "p.Asn243Ser",
"transcript": "ENST00000893861.1",
"protein_id": "ENSP00000563920.1",
"transcript_support_level": null,
"aa_start": 243,
"aa_end": null,
"aa_length": 320,
"cds_start": 728,
"cds_end": null,
"cds_length": 963,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893861.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.509A>G",
"hgvs_p": "p.Asn170Ser",
"transcript": "ENST00000893869.1",
"protein_id": "ENSP00000563928.1",
"transcript_support_level": null,
"aa_start": 170,
"aa_end": null,
"aa_length": 247,
"cds_start": 509,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893869.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.407A>G",
"hgvs_p": "p.Asn136Ser",
"transcript": "ENST00000893866.1",
"protein_id": "ENSP00000563925.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 213,
"cds_start": 407,
"cds_end": null,
"cds_length": 642,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893866.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.362A>G",
"hgvs_p": "p.Asn121Ser",
"transcript": "ENST00000930431.1",
"protein_id": "ENSP00000600490.1",
"transcript_support_level": null,
"aa_start": 121,
"aa_end": null,
"aa_length": 198,
"cds_start": 362,
"cds_end": null,
"cds_length": 597,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930431.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "c.245-87A>G",
"hgvs_p": null,
"transcript": "ENST00000930430.1",
"protein_id": "ENSP00000600489.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 130,
"cds_start": null,
"cds_end": null,
"cds_length": 393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000930430.1"
},
{
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "n.540A>G",
"hgvs_p": null,
"transcript": "ENST00000480048.5",
"protein_id": null,
"transcript_support_level": 4,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000480048.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"hgvs_c": "n.*624A>G",
"hgvs_p": null,
"transcript": "ENST00000455824.1",
"protein_id": "ENSP00000397062.1",
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000455824.1"
}
],
"gene_symbol": "ST13",
"gene_hgnc_id": 11343,
"dbsnp": "rs144283288",
"frequency_reference_population": 0.0016783786,
"hom_count_reference_population": 45,
"allele_count_reference_population": 2708,
"gnomad_exomes_af": 0.000932099,
"gnomad_genomes_af": 0.00884107,
"gnomad_exomes_ac": 1362,
"gnomad_genomes_ac": 1346,
"gnomad_exomes_homalt": 27,
"gnomad_genomes_homalt": 18,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0031644701957702637,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.124,
"revel_prediction": "Benign",
"alphamissense_score": 0.0486,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.51,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.483,
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_003932.5",
"gene_symbol": "ST13",
"hgnc_id": 11343,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.875A>G",
"hgvs_p": "p.Asn292Ser"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}