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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: 1-111315400-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=111315400&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 111315400,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_201653.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.445C>T",
"hgvs_p": "p.Pro149Ser",
"transcript": "NM_201653.4",
"protein_id": "NP_970615.2",
"transcript_support_level": null,
"aa_start": 149,
"aa_end": null,
"aa_length": 476,
"cds_start": 445,
"cds_end": null,
"cds_length": 1431,
"cdna_start": 613,
"cdna_end": null,
"cdna_length": 1696,
"mane_select": "ENST00000369740.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.445C>T",
"hgvs_p": "p.Pro149Ser",
"transcript": "ENST00000369740.6",
"protein_id": "ENSP00000358755.1",
"transcript_support_level": 1,
"aa_start": 149,
"aa_end": null,
"aa_length": 476,
"cds_start": 445,
"cds_end": null,
"cds_length": 1431,
"cdna_start": 613,
"cdna_end": null,
"cdna_length": 1696,
"mane_select": "NM_201653.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.277C>T",
"hgvs_p": "p.Pro93Ser",
"transcript": "ENST00000422815.5",
"protein_id": "ENSP00000387671.1",
"transcript_support_level": 1,
"aa_start": 93,
"aa_end": null,
"aa_length": 420,
"cds_start": 277,
"cds_end": null,
"cds_length": 1263,
"cdna_start": 277,
"cdna_end": null,
"cdna_length": 1354,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.121C>T",
"hgvs_p": "p.Pro41Ser",
"transcript": "ENST00000430615.1",
"protein_id": "ENSP00000391132.1",
"transcript_support_level": 1,
"aa_start": 41,
"aa_end": null,
"aa_length": 368,
"cds_start": 121,
"cds_end": null,
"cds_length": 1107,
"cdna_start": 234,
"cdna_end": null,
"cdna_length": 1320,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"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": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "n.121C>T",
"hgvs_p": null,
"transcript": "ENST00000352594.10",
"protein_id": "ENSP00000271312.8",
"transcript_support_level": 1,
"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": 1482,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 10,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-142-334C>T",
"hgvs_p": null,
"transcript": "ENST00000353665.10",
"protein_id": "ENSP00000338970.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1214,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 9,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-4+804C>T",
"hgvs_p": null,
"transcript": "ENST00000451398.6",
"protein_id": "ENSP00000390476.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1256,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 8,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-4+804C>T",
"hgvs_p": null,
"transcript": "ENST00000483391.5",
"protein_id": "ENSP00000436946.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1188,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 9,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-4+804C>T",
"hgvs_p": null,
"transcript": "ENST00000489524.5",
"protein_id": "ENSP00000433309.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 286,
"cds_start": -4,
"cds_end": null,
"cds_length": 862,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 977,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.445C>T",
"hgvs_p": "p.Pro149Ser",
"transcript": "ENST00000343320.10",
"protein_id": "ENSP00000341828.6",
"transcript_support_level": 5,
"aa_start": 149,
"aa_end": null,
"aa_length": 476,
"cds_start": 445,
"cds_end": null,
"cds_length": 1431,
"cdna_start": 539,
"cdna_end": null,
"cdna_length": 1624,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.121C>T",
"hgvs_p": "p.Pro41Ser",
"transcript": "NM_001258001.2",
"protein_id": "NP_001244930.1",
"transcript_support_level": null,
"aa_start": 41,
"aa_end": null,
"aa_length": 368,
"cds_start": 121,
"cds_end": null,
"cds_length": 1107,
"cdna_start": 411,
"cdna_end": null,
"cdna_length": 1494,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.121C>T",
"hgvs_p": "p.Pro41Ser",
"transcript": "NM_001258003.2",
"protein_id": "NP_001244932.1",
"transcript_support_level": null,
"aa_start": 41,
"aa_end": null,
"aa_length": 368,
"cds_start": 121,
"cds_end": null,
"cds_length": 1107,
"cdna_start": 318,
"cdna_end": null,
"cdna_length": 1401,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.121C>T",
"hgvs_p": "p.Pro41Ser",
"transcript": "NM_021797.4",
"protein_id": "NP_068569.2",
"transcript_support_level": null,
"aa_start": 41,
"aa_end": null,
"aa_length": 368,
"cds_start": 121,
"cds_end": null,
"cds_length": 1107,
"cdna_start": 288,
"cdna_end": null,
"cdna_length": 1371,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "n.923C>T",
"hgvs_p": null,
"transcript": "ENST00000477918.6",
"protein_id": null,
"transcript_support_level": 2,
"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": 4250,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-178C>T",
"hgvs_p": null,
"transcript": "NM_001258004.2",
"protein_id": "NP_001244933.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1633,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 10,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-4+804C>T",
"hgvs_p": null,
"transcript": "NM_001040623.3",
"protein_id": "NP_001035713.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1328,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 8,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-4+804C>T",
"hgvs_p": null,
"transcript": "NM_001258002.2",
"protein_id": "NP_001244931.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1205,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 11,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"hgvs_c": "c.-142-334C>T",
"hgvs_p": null,
"transcript": "NM_001258005.2",
"protein_id": "NP_001244934.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 315,
"cds_start": -4,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1467,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CHIA",
"gene_hgnc_id": 17432,
"dbsnp": "rs772586251",
"frequency_reference_population": 0.000019826444,
"hom_count_reference_population": 0,
"allele_count_reference_population": 32,
"gnomad_exomes_af": 0.0000191541,
"gnomad_genomes_af": 0.000026285,
"gnomad_exomes_ac": 28,
"gnomad_genomes_ac": 4,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.07489526271820068,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.023,
"revel_prediction": "Benign",
"alphamissense_score": 0.0901,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.73,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.394,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_201653.4",
"gene_symbol": "CHIA",
"hgnc_id": 17432,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.445C>T",
"hgvs_p": "p.Pro149Ser"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}