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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: 6-38923068-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=38923068&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 38923068,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001206927.2",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 72,
"exon_rank_end": null,
"exon_count": 93,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr",
"transcript": "NM_001206927.2",
"protein_id": "NP_001193856.1",
"transcript_support_level": null,
"aa_start": 3558,
"aa_end": null,
"aa_length": 4707,
"cds_start": 10673,
"cds_end": null,
"cds_length": 14124,
"cdna_start": 10812,
"cdna_end": null,
"cdna_length": 14663,
"mane_select": "ENST00000327475.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 72,
"exon_rank_end": null,
"exon_count": 93,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr",
"transcript": "ENST00000327475.11",
"protein_id": "ENSP00000333363.7",
"transcript_support_level": 5,
"aa_start": 3558,
"aa_end": null,
"aa_length": 4707,
"cds_start": 10673,
"cds_end": null,
"cds_length": 14124,
"cdna_start": 10812,
"cdna_end": null,
"cdna_length": 14663,
"mane_select": "NM_001206927.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 71,
"exon_rank_end": null,
"exon_count": 92,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10022A>C",
"hgvs_p": "p.Asn3341Thr",
"transcript": "NM_001371.4",
"protein_id": "NP_001362.2",
"transcript_support_level": null,
"aa_start": 3341,
"aa_end": null,
"aa_length": 4490,
"cds_start": 10022,
"cds_end": null,
"cds_length": 13473,
"cdna_start": 10727,
"cdna_end": null,
"cdna_length": 14578,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 70,
"exon_rank_end": null,
"exon_count": 91,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10022A>C",
"hgvs_p": "p.Asn3341Thr",
"transcript": "ENST00000359357.7",
"protein_id": "ENSP00000352312.3",
"transcript_support_level": 2,
"aa_start": 3341,
"aa_end": null,
"aa_length": 4490,
"cds_start": 10022,
"cds_end": null,
"cds_length": 13473,
"cdna_start": 10276,
"cdna_end": null,
"cdna_length": 13864,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 71,
"exon_rank_end": null,
"exon_count": 82,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr",
"transcript": "ENST00000449981.6",
"protein_id": "ENSP00000415331.2",
"transcript_support_level": 5,
"aa_start": 3558,
"aa_end": null,
"aa_length": 4188,
"cds_start": 10673,
"cds_end": null,
"cds_length": 12567,
"cdna_start": 10673,
"cdna_end": null,
"cdna_length": 12940,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 71,
"exon_rank_end": null,
"exon_count": 92,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10610A>C",
"hgvs_p": "p.Asn3537Thr",
"transcript": "XM_011514318.3",
"protein_id": "XP_011512620.1",
"transcript_support_level": null,
"aa_start": 3537,
"aa_end": null,
"aa_length": 4686,
"cds_start": 10610,
"cds_end": null,
"cds_length": 14061,
"cdna_start": 10749,
"cdna_end": null,
"cdna_length": 14600,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 71,
"exon_rank_end": null,
"exon_count": 92,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10565A>C",
"hgvs_p": "p.Asn3522Thr",
"transcript": "XM_011514319.3",
"protein_id": "XP_011512621.1",
"transcript_support_level": null,
"aa_start": 3522,
"aa_end": null,
"aa_length": 4671,
"cds_start": 10565,
"cds_end": null,
"cds_length": 14016,
"cdna_start": 10704,
"cdna_end": null,
"cdna_length": 14555,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 70,
"exon_rank_end": null,
"exon_count": 91,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10436A>C",
"hgvs_p": "p.Asn3479Thr",
"transcript": "XM_011514320.3",
"protein_id": "XP_011512622.1",
"transcript_support_level": null,
"aa_start": 3479,
"aa_end": null,
"aa_length": 4628,
"cds_start": 10436,
"cds_end": null,
"cds_length": 13887,
"cdna_start": 10575,
"cdna_end": null,
"cdna_length": 14426,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 72,
"exon_rank_end": null,
"exon_count": 89,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr",
"transcript": "XM_017010325.2",
"protein_id": "XP_016865814.1",
"transcript_support_level": null,
"aa_start": 3558,
"aa_end": null,
"aa_length": 4459,
"cds_start": 10673,
"cds_end": null,
"cds_length": 13380,
"cdna_start": 10812,
"cdna_end": null,
"cdna_length": 14479,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 72,
"exon_rank_end": null,
"exon_count": 81,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr",
"transcript": "XM_017010326.2",
"protein_id": "XP_016865815.1",
"transcript_support_level": null,
"aa_start": 3558,
"aa_end": null,
"aa_length": 4081,
"cds_start": 10673,
"cds_end": null,
"cds_length": 12246,
"cdna_start": 10812,
"cdna_end": null,
"cdna_length": 12466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8-AS1",
"gene_hgnc_id": 40188,
"hgvs_c": "n.791T>G",
"hgvs_p": null,
"transcript": "ENST00000416948.1",
"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": 830,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8-AS1",
"gene_hgnc_id": 40188,
"hgvs_c": "n.714T>G",
"hgvs_p": null,
"transcript": "ENST00000418399.5",
"protein_id": null,
"transcript_support_level": 3,
"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": 753,
"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": 72,
"exon_rank_end": null,
"exon_count": 94,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"hgvs_c": "n.10812A>C",
"hgvs_p": null,
"transcript": "XR_926078.3",
"protein_id": null,
"transcript_support_level": null,
"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": 14253,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "DNAH8-AS1",
"gene_hgnc_id": 40188,
"hgvs_c": "n.782+17T>G",
"hgvs_p": null,
"transcript": "NR_038401.1",
"protein_id": null,
"transcript_support_level": null,
"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": 2125,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "DNAH8",
"gene_hgnc_id": 2952,
"dbsnp": "rs1308574895",
"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": 0.3601610064506531,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.259,
"revel_prediction": "Benign",
"alphamissense_score": 0.1096,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.27,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 7.398,
"phylop100way_prediction": "Uncertain_significance",
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001206927.2",
"gene_symbol": "DNAH8",
"hgnc_id": 2952,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.10673A>C",
"hgvs_p": "p.Asn3558Thr"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000416948.1",
"gene_symbol": "DNAH8-AS1",
"hgnc_id": 40188,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.791T>G",
"hgvs_p": null
}
],
"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
}