← Back to variant description
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: 3-48590721-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=48590721&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 48590721,
"ref": "G",
"alt": "A",
"effect": "stop_gained",
"transcript": "NM_000094.4",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 119,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "NM_000094.4",
"protein_id": "NP_000085.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2944,
"cds_start": 1732,
"cds_end": null,
"cds_length": 8835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000681320.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000094.4"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 119,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "ENST00000681320.1",
"protein_id": "ENSP00000506558.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2944,
"cds_start": 1732,
"cds_end": null,
"cds_length": 8835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000094.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000681320.1"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 118,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "ENST00000328333.12",
"protein_id": "ENSP00000332371.8",
"transcript_support_level": 1,
"aa_start": 578,
"aa_end": null,
"aa_length": 2944,
"cds_start": 1732,
"cds_end": null,
"cds_length": 8835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000328333.12"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 118,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "XM_017005688.2",
"protein_id": "XP_016861177.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2924,
"cds_start": 1732,
"cds_end": null,
"cds_length": 8775,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017005688.2"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 106,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "XM_017005689.2",
"protein_id": "XP_016861178.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2609,
"cds_start": 1732,
"cds_end": null,
"cds_length": 7830,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017005689.2"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 98,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "XM_017005690.2",
"protein_id": "XP_016861179.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2470,
"cds_start": 1732,
"cds_end": null,
"cds_length": 7413,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017005690.2"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 98,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "XM_017005691.2",
"protein_id": "XP_016861180.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2466,
"cds_start": 1732,
"cds_end": null,
"cds_length": 7401,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017005691.2"
},
{
"aa_ref": "R",
"aa_alt": "*",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"stop_gained"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 99,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*",
"transcript": "XM_017005692.2",
"protein_id": "XP_016861181.1",
"transcript_support_level": null,
"aa_start": 578,
"aa_end": null,
"aa_length": 2452,
"cds_start": 1732,
"cds_end": null,
"cds_length": 7359,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017005692.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 118,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740003.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740003.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 118,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740004.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740004.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 118,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740005.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740005.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 101,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740006.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740006.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 96,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740007.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740007.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 90,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740008.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740008.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 78,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"hgvs_c": "n.1795C>T",
"hgvs_p": null,
"transcript": "XR_001740009.2",
"protein_id": null,
"transcript_support_level": null,
"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": "XR_001740009.2"
}
],
"gene_symbol": "COL7A1",
"gene_hgnc_id": 2214,
"dbsnp": "rs144023803",
"frequency_reference_population": 0.000116488154,
"hom_count_reference_population": 0,
"allele_count_reference_population": 188,
"gnomad_exomes_af": 0.000126564,
"gnomad_genomes_af": 0.0000197132,
"gnomad_exomes_ac": 185,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.550000011920929,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.55,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 5.328,
"phylop100way_prediction": "Uncertain_significance",
"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": 16,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PVS1,PP5_Very_Strong",
"acmg_by_gene": [
{
"score": 16,
"benign_score": 0,
"pathogenic_score": 16,
"criteria": [
"PVS1",
"PP5_Very_Strong"
],
"verdict": "Pathogenic",
"transcript": "NM_000094.4",
"gene_symbol": "COL7A1",
"hgnc_id": 2214,
"effects": [
"stop_gained"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.1732C>T",
"hgvs_p": "p.Arg578*"
}
],
"clinvar_disease": "7 conditions,COL7A1-related disorder,Epidermolysis bullosa dystrophica,Epidermolysis bullosa pruriginosa,Generalized dominant dystrophic epidermolysis bullosa,Recessive dystrophic epidermolysis bullosa,See cases,not provided",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:8 O:1",
"phenotype_combined": "not provided|7 conditions|Recessive dystrophic epidermolysis bullosa|Epidermolysis bullosa dystrophica|COL7A1-related disorder|Generalized dominant dystrophic epidermolysis bullosa|See cases|Epidermolysis bullosa pruriginosa",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}