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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: 12-131725611-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=131725611&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 131725611,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001261411.2",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "NM_004592.4",
"protein_id": "NP_004583.2",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 951,
"cds_start": 813,
"cds_end": null,
"cds_length": 2856,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000261674.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004592.4"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "ENST00000261674.9",
"protein_id": "ENSP00000261674.4",
"transcript_support_level": 1,
"aa_start": 271,
"aa_end": null,
"aa_length": 951,
"cds_start": 813,
"cds_end": null,
"cds_length": 2856,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_004592.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000261674.9"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "ENST00000541286.5",
"protein_id": "ENSP00000437738.1",
"transcript_support_level": 1,
"aa_start": 271,
"aa_end": null,
"aa_length": 1003,
"cds_start": 813,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000541286.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "n.4147C>A",
"hgvs_p": null,
"transcript": "ENST00000535236.5",
"protein_id": null,
"transcript_support_level": 1,
"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": "ENST00000535236.5"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "NM_001261411.2",
"protein_id": "NP_001248340.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 1003,
"cds_start": 813,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001261411.2"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "ENST00000938425.1",
"protein_id": "ENSP00000608484.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 950,
"cds_start": 813,
"cds_end": null,
"cds_length": 2853,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938425.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "ENST00000938426.1",
"protein_id": "ENSP00000608485.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 929,
"cds_start": 813,
"cds_end": null,
"cds_length": 2790,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938426.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "XM_011538653.1",
"protein_id": "XP_011536955.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 926,
"cds_start": 813,
"cds_end": null,
"cds_length": 2781,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538653.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.435C>A",
"hgvs_p": "p.Asn145Lys",
"transcript": "XM_024449125.1",
"protein_id": "XP_024304893.1",
"transcript_support_level": null,
"aa_start": 145,
"aa_end": null,
"aa_length": 877,
"cds_start": 435,
"cds_end": null,
"cds_length": 2634,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024449125.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "XM_017019798.1",
"protein_id": "XP_016875287.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 874,
"cds_start": 813,
"cds_end": null,
"cds_length": 2625,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017019798.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys",
"transcript": "XM_011538655.3",
"protein_id": "XP_011536957.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 834,
"cds_start": 813,
"cds_end": null,
"cds_length": 2505,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538655.3"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.435C>A",
"hgvs_p": "p.Asn145Lys",
"transcript": "XM_047429327.1",
"protein_id": "XP_047285283.1",
"transcript_support_level": null,
"aa_start": 145,
"aa_end": null,
"aa_length": 825,
"cds_start": 435,
"cds_end": null,
"cds_length": 2478,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047429327.1"
},
{
"aa_ref": "N",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.435C>A",
"hgvs_p": "p.Asn145Lys",
"transcript": "XM_047429328.1",
"protein_id": "XP_047285284.1",
"transcript_support_level": null,
"aa_start": 145,
"aa_end": null,
"aa_length": 800,
"cds_start": 435,
"cds_end": null,
"cds_length": 2403,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047429328.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "c.218+14164C>A",
"hgvs_p": null,
"transcript": "ENST00000874197.1",
"protein_id": "ENSP00000544256.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 221,
"cds_start": null,
"cds_end": null,
"cds_length": 666,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000874197.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "n.*400C>A",
"hgvs_p": null,
"transcript": "ENST00000538548.5",
"protein_id": "ENSP00000445832.1",
"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": "ENST00000538548.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "n.259C>A",
"hgvs_p": null,
"transcript": "ENST00000542813.2",
"protein_id": null,
"transcript_support_level": 3,
"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": "pseudogene",
"feature": "ENST00000542813.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "n.*400C>A",
"hgvs_p": null,
"transcript": "ENST00000538548.5",
"protein_id": "ENSP00000445832.1",
"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": "ENST00000538548.5"
},
{
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"hgvs_c": "n.*2C>A",
"hgvs_p": null,
"transcript": "ENST00000540469.5",
"protein_id": null,
"transcript_support_level": 3,
"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": "ENST00000540469.5"
}
],
"gene_symbol": "SFSWAP",
"gene_hgnc_id": 10790,
"dbsnp": "rs147670551",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.04851880669593811,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.045,
"revel_prediction": "Benign",
"alphamissense_score": 0.1201,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.79,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.39,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_001261411.2",
"gene_symbol": "SFSWAP",
"hgnc_id": 10790,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.813C>A",
"hgvs_p": "p.Asn271Lys"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}