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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: 7-761781-GT-AC (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=761781&ref=GT&alt=AC&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM5"
],
"effects": [
"missense_variant"
],
"gene_symbol": "DNAAF5",
"hgnc_id": 26013,
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"inheritance_mode": "AR,AD",
"pathogenic_score": 2,
"score": 2,
"transcript": "NM_017802.4",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM5",
"acmg_score": 2,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "AC",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "7",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 855,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3412,
"cdna_start": 1521,
"cds_end": null,
"cds_length": 2568,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_017802.4",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000297440.11",
"protein_coding": true,
"protein_id": "NP_060272.3",
"strand": true,
"transcript": "NM_017802.4",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 855,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3412,
"cdna_start": 1521,
"cds_end": null,
"cds_length": 2568,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000297440.11",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_017802.4",
"protein_coding": true,
"protein_id": "ENSP00000297440.6",
"strand": true,
"transcript": "ENST00000297440.11",
"transcript_support_level": 1
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 882,
"aa_ref": "C",
"aa_start": 527,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3488,
"cdna_start": 1599,
"cds_end": null,
"cds_length": 2649,
"cds_start": 1580,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000852634.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1580_1581delGTinsAC",
"hgvs_p": "p.Cys527Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000522693.1",
"strand": true,
"transcript": "ENST00000852634.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 862,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3430,
"cdna_start": 1518,
"cds_end": null,
"cds_length": 2589,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000852633.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000522692.1",
"strand": true,
"transcript": "ENST00000852633.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 853,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2972,
"cdna_start": 1521,
"cds_end": null,
"cds_length": 2562,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000852635.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000522694.1",
"strand": true,
"transcript": "ENST00000852635.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 830,
"aa_ref": "C",
"aa_start": 475,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3344,
"cdna_start": 1453,
"cds_end": null,
"cds_length": 2493,
"cds_start": 1424,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000913166.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1424_1425delGTinsAC",
"hgvs_p": "p.Cys475Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000583225.1",
"strand": true,
"transcript": "ENST00000913166.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 791,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3227,
"cdna_start": 1528,
"cds_end": null,
"cds_length": 2376,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000852632.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000522691.1",
"strand": true,
"transcript": "ENST00000852632.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 712,
"aa_ref": "C",
"aa_start": 357,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2992,
"cdna_start": 1101,
"cds_end": null,
"cds_length": 2139,
"cds_start": 1070,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000852631.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1070_1071delGTinsAC",
"hgvs_p": "p.Cys357Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000522690.1",
"strand": true,
"transcript": "ENST00000852631.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 656,
"aa_ref": "C",
"aa_start": 301,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2350,
"cdna_start": 903,
"cds_end": null,
"cds_length": 1971,
"cds_start": 902,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000440747.5",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.902_903delGTinsAC",
"hgvs_p": "p.Cys301Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000403165.1",
"strand": true,
"transcript": "ENST00000440747.5",
"transcript_support_level": 2
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 648,
"aa_ref": "C",
"aa_start": 357,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2784,
"cdna_start": 1088,
"cds_end": null,
"cds_length": 1947,
"cds_start": 1070,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000913167.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1070_1071delGTinsAC",
"hgvs_p": "p.Cys357Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000583226.1",
"strand": true,
"transcript": "ENST00000913167.1",
"transcript_support_level": null
},
{
"aa_alt": "Y",
"aa_end": null,
"aa_length": 791,
"aa_ref": "C",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3220,
"cdna_start": 1521,
"cds_end": null,
"cds_length": 2376,
"cds_start": 1499,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_024446813.2",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1499_1500delGTinsAC",
"hgvs_p": "p.Cys500Tyr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_024302581.1",
"strand": true,
"transcript": "XM_024446813.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 602,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2646,
"cdna_start": null,
"cds_end": null,
"cds_length": 1809,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000972191.1",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "c.1025-8690_1025-8689delGTinsAC",
"hgvs_p": null,
"intron_rank": 4,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000642250.1",
"strand": true,
"transcript": "ENST00000972191.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3350,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "NR_075098.2",
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"hgvs_c": "n.1459_1460delGTinsAC",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_075098.2",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": null,
"effect": "missense_variant",
"frequency_reference_population": null,
"gene_hgnc_id": 26013,
"gene_symbol": "DNAAF5",
"gnomad_exomes_ac": null,
"gnomad_exomes_af": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_ac": null,
"gnomad_genomes_af": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": null,
"phenotype_combined": null,
"phylop100way_prediction": "Uncertain_significance",
"phylop100way_score": 7.15,
"pos": 761781,
"ref": "GT",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": null,
"splice_score_selected": null,
"splice_source_selected": null,
"spliceai_max_prediction": null,
"spliceai_max_score": null,
"transcript": "NM_017802.4"
}
]
}