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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: 1-9244919-CCCCAGGCA-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=9244919&ref=CCCCAGGCA&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 9244919,
"ref": "CCCCAGGCA",
"alt": "C",
"effect": "splice_acceptor_variant,splice_region_variant,5_prime_UTR_variant,intron_variant",
"transcript": "ENST00000377403.7",
"consequences": [
{
"aa_ref": "M",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant",
"start_lost"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-7_1delCCCAGGCA",
"hgvs_p": "p.Met1fs",
"transcript": "NM_004285.4",
"protein_id": "NP_004276.2",
"transcript_support_level": null,
"aa_start": 1,
"aa_end": null,
"aa_length": 791,
"cds_start": 1,
"cds_end": null,
"cds_length": 2376,
"cdna_start": 297,
"cdna_end": null,
"cdna_length": 9147,
"mane_select": "ENST00000377403.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_region_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-10-5_-8delCCCAGGCA",
"hgvs_p": null,
"transcript": "ENST00000377403.7",
"protein_id": "ENSP00000366620.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9147,
"mane_select": "NM_004285.4",
"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": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-7_1delCCCAGGCA",
"hgvs_p": null,
"transcript": "NM_004285.4",
"protein_id": "NP_004276.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9147,
"mane_select": "ENST00000377403.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_acceptor_variant",
"splice_region_variant",
"5_prime_UTR_variant",
"intron_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-10-5_-8delCCCAGGCA",
"hgvs_p": null,
"transcript": "ENST00000377403.7",
"protein_id": "ENSP00000366620.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9147,
"mane_select": "NM_004285.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "WH",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_acceptor_variant",
"disruptive_inframe_deletion",
"splice_region_variant",
"intron_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.24-5_26delCCCAGGCA",
"hgvs_p": "p.Trp8_His9delinsCys",
"transcript": "ENST00000602477.1",
"protein_id": "ENSP00000473348.1",
"transcript_support_level": 1,
"aa_start": 8,
"aa_end": null,
"aa_length": 802,
"cds_start": 24,
"cds_end": null,
"cds_length": 2409,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5590,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"non_coding_transcript_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-10-5_-8delCCCAGGCA",
"hgvs_p": null,
"transcript": "ENST00000377403.7",
"protein_id": "ENSP00000366620.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9147,
"mane_select": "NM_004285.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "HPGM",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.27_34delCCCAGGCA",
"hgvs_p": "p.Pro10fs",
"transcript": "NM_001282587.2",
"protein_id": "NP_001269516.1",
"transcript_support_level": null,
"aa_start": 9,
"aa_end": null,
"aa_length": 802,
"cds_start": 27,
"cds_end": null,
"cds_length": 2409,
"cdna_start": 176,
"cdna_end": null,
"cdna_length": 9026,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "HPGM",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.27_34delCCCAGGCA",
"hgvs_p": "p.Pro10fs",
"transcript": "XM_047435002.1",
"protein_id": "XP_047290958.1",
"transcript_support_level": null,
"aa_start": 9,
"aa_end": null,
"aa_length": 802,
"cds_start": 27,
"cds_end": null,
"cds_length": 2409,
"cdna_start": 501,
"cdna_end": null,
"cdna_length": 9351,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "HPGM",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.21_28delCCCAGGCA",
"hgvs_p": "p.Pro8fs",
"transcript": "XM_005263540.6",
"protein_id": "XP_005263597.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 800,
"cds_start": 21,
"cds_end": null,
"cds_length": 2403,
"cdna_start": 152,
"cdna_end": null,
"cdna_length": 9002,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "HPGM",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.15_22delCCCAGGCA",
"hgvs_p": "p.Pro6fs",
"transcript": "XM_047435003.1",
"protein_id": "XP_047290959.1",
"transcript_support_level": null,
"aa_start": 5,
"aa_end": null,
"aa_length": 798,
"cds_start": 15,
"cds_end": null,
"cds_length": 2397,
"cdna_start": 146,
"cdna_end": null,
"cdna_length": 8996,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant",
"start_lost"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-7_1delCCCAGGCA",
"hgvs_p": "p.Met1fs",
"transcript": "XM_047435005.1",
"protein_id": "XP_047290961.1",
"transcript_support_level": null,
"aa_start": 1,
"aa_end": null,
"aa_length": 791,
"cds_start": 1,
"cds_end": null,
"cds_length": 2376,
"cdna_start": 166,
"cdna_end": null,
"cdna_length": 9016,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"start_lost",
"conservative_inframe_deletion",
"splice_region_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-2-5_1delCCCAGGCA",
"hgvs_p": "p.Met1del",
"transcript": "XM_006711052.5",
"protein_id": "XP_006711115.1",
"transcript_support_level": null,
"aa_start": 1,
"aa_end": null,
"aa_length": 791,
"cds_start": 1,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9139,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"start_lost",
"conservative_inframe_deletion",
"splice_region_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-2-5_1delCCCAGGCA",
"hgvs_p": "p.Met1del",
"transcript": "XM_017002865.3",
"protein_id": "XP_016858354.1",
"transcript_support_level": null,
"aa_start": 1,
"aa_end": null,
"aa_length": 791,
"cds_start": 1,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9018,
"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": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-7_1delCCCAGGCA",
"hgvs_p": null,
"transcript": "XM_047435005.1",
"protein_id": "XP_047290961.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9016,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_acceptor_variant",
"5_prime_UTR_truncation",
"exon_loss_variant",
"splice_region_variant",
"intron_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-2-5_1delCCCAGGCA",
"hgvs_p": null,
"transcript": "XM_006711052.5",
"protein_id": "XP_006711115.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9139,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"splice_acceptor_variant",
"5_prime_UTR_truncation",
"exon_loss_variant",
"splice_region_variant",
"intron_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"hgvs_c": "c.-2-5_1delCCCAGGCA",
"hgvs_p": null,
"transcript": "XM_017002865.3",
"protein_id": "XP_016858354.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 791,
"cds_start": -4,
"cds_end": null,
"cds_length": 2376,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9018,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "H6PD",
"gene_hgnc_id": 4795,
"dbsnp": null,
"frequency_reference_population": 0.1442441,
"hom_count_reference_population": 18758,
"allele_count_reference_population": 232128,
"gnomad_exomes_af": 0.146442,
"gnomad_genomes_af": 0.123193,
"gnomad_exomes_ac": 213384,
"gnomad_genomes_ac": 18744,
"gnomad_exomes_homalt": 17265,
"gnomad_genomes_homalt": 1493,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": null,
"computational_prediction_selected": null,
"computational_source_selected": null,
"splice_score_selected": null,
"splice_prediction_selected": null,
"splice_source_selected": null,
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 1.773,
"phylop100way_prediction": "Benign",
"spliceai_max_score": null,
"spliceai_max_prediction": null,
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -12,
"acmg_classification": "Benign",
"acmg_criteria": "PVS1_Strong,BP6_Very_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 16,
"pathogenic_score": 4,
"criteria": [
"PVS1_Strong",
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000377403.7",
"gene_symbol": "H6PD",
"hgnc_id": 4795,
"effects": [
"splice_acceptor_variant",
"splice_region_variant",
"5_prime_UTR_variant",
"intron_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.-10-5_-8delCCCAGGCA",
"hgvs_p": null
}
],
"clinvar_disease": "Cortisone reductase deficiency 1,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not specified|Cortisone reductase deficiency 1",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}