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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: 11-557985-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=557985&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 557985,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000329451.8",
"consequences": [
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.454A>G",
"hgvs_p": "p.Met152Val",
"transcript": "NM_173573.3",
"protein_id": "NP_775844.2",
"transcript_support_level": null,
"aa_start": 152,
"aa_end": null,
"aa_length": 634,
"cds_start": 454,
"cds_end": null,
"cds_length": 1905,
"cdna_start": 476,
"cdna_end": null,
"cdna_length": 2057,
"mane_select": "ENST00000329451.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.454A>G",
"hgvs_p": "p.Met152Val",
"transcript": "ENST00000329451.8",
"protein_id": "ENSP00000331167.3",
"transcript_support_level": 1,
"aa_start": 152,
"aa_end": null,
"aa_length": 634,
"cds_start": 454,
"cds_end": null,
"cds_length": 1905,
"cdna_start": 476,
"cdna_end": null,
"cdna_length": 2057,
"mane_select": "NM_173573.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.475A>G",
"hgvs_p": "p.Met159Val",
"transcript": "ENST00000441853.5",
"protein_id": "ENSP00000393529.1",
"transcript_support_level": 3,
"aa_start": 159,
"aa_end": null,
"aa_length": 301,
"cds_start": 475,
"cds_end": null,
"cds_length": 906,
"cdna_start": 620,
"cdna_end": null,
"cdna_length": 1051,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.484A>G",
"hgvs_p": "p.Met162Val",
"transcript": "ENST00000486629.1",
"protein_id": "ENSP00000435529.1",
"transcript_support_level": 5,
"aa_start": 162,
"aa_end": null,
"aa_length": 246,
"cds_start": 484,
"cds_end": null,
"cds_length": 743,
"cdna_start": 539,
"cdna_end": null,
"cdna_length": 798,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.673A>G",
"hgvs_p": "p.Met225Val",
"transcript": "XM_011519965.3",
"protein_id": "XP_011518267.2",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 707,
"cds_start": 673,
"cds_end": null,
"cds_length": 2124,
"cdna_start": 1827,
"cdna_end": null,
"cdna_length": 3408,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.658A>G",
"hgvs_p": "p.Met220Val",
"transcript": "XM_047426712.1",
"protein_id": "XP_047282668.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 702,
"cds_start": 658,
"cds_end": null,
"cds_length": 2109,
"cdna_start": 1812,
"cdna_end": null,
"cdna_length": 3393,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.673A>G",
"hgvs_p": "p.Met225Val",
"transcript": "XM_011519967.3",
"protein_id": "XP_011518269.2",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 667,
"cds_start": 673,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1827,
"cdna_end": null,
"cdna_length": 3288,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.469A>G",
"hgvs_p": "p.Met157Val",
"transcript": "XM_047426713.1",
"protein_id": "XP_047282669.1",
"transcript_support_level": null,
"aa_start": 157,
"aa_end": null,
"aa_length": 639,
"cds_start": 469,
"cds_end": null,
"cds_length": 1920,
"cdna_start": 491,
"cdna_end": null,
"cdna_length": 2072,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.673A>G",
"hgvs_p": "p.Met225Val",
"transcript": "XM_017017479.3",
"protein_id": "XP_016872968.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 630,
"cds_start": 673,
"cds_end": null,
"cds_length": 1893,
"cdna_start": 1827,
"cdna_end": null,
"cdna_length": 3126,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"hgvs_c": "c.673A>G",
"hgvs_p": "p.Met225Val",
"transcript": "XM_047426714.1",
"protein_id": "XP_047282670.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 406,
"cds_start": 673,
"cds_end": null,
"cds_length": 1221,
"cdna_start": 1827,
"cdna_end": null,
"cdna_length": 2471,
"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": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMNTD2-AS1",
"gene_hgnc_id": 41204,
"hgvs_c": "n.391T>C",
"hgvs_p": null,
"transcript": "ENST00000527620.5",
"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": 2210,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "LMNTD2",
"gene_hgnc_id": 28561,
"dbsnp": "rs1853007415",
"frequency_reference_population": 0.0000048353695,
"hom_count_reference_population": 0,
"allele_count_reference_population": 7,
"gnomad_exomes_af": 0.00000483537,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 7,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.038553833961486816,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.033,
"revel_prediction": "Benign",
"alphamissense_score": 0.0682,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.57,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.32,
"phylop100way_prediction": "Benign",
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong,BP6_Moderate",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 6,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000329451.8",
"gene_symbol": "LMNTD2",
"hgnc_id": 28561,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.454A>G",
"hgvs_p": "p.Met152Val"
},
{
"score": -4,
"benign_score": 6,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000527620.5",
"gene_symbol": "LMNTD2-AS1",
"hgnc_id": 41204,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.391T>C",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}