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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: 12-49040600-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=49040600&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 14,
"criteria": [
"BP4_Strong",
"BP6",
"BP7",
"BS1",
"BS2"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "KMT2D",
"hgnc_id": 7133,
"hgvs_c": "c.7170G>A",
"hgvs_p": "p.Pro2390Pro",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -14,
"transcript": "NM_003482.4",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BP7,BS1,BS2",
"acmg_score": -14,
"allele_count_reference_population": 95,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.76,
"chr": "12",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": "Kabuki syndrome,Kabuki syndrome 1",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:1 LB:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.7599999904632568,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 5537,
"aa_ref": "P",
"aa_start": 2390,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 20635,
"cdna_start": 8389,
"cds_end": null,
"cds_length": 16614,
"cds_start": 7170,
"consequences": [
"synonymous_variant"
],
"exon_count": 55,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "NM_003482.4",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.7170G>A",
"hgvs_p": "p.Pro2390Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000301067.12",
"protein_coding": true,
"protein_id": "NP_003473.3",
"strand": false,
"transcript": "NM_003482.4",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 5537,
"aa_ref": "P",
"aa_start": 2390,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 20635,
"cdna_start": 8389,
"cds_end": null,
"cds_length": 16614,
"cds_start": 7170,
"consequences": [
"synonymous_variant"
],
"exon_count": 55,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000301067.12",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.7170G>A",
"hgvs_p": "p.Pro2390Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_003482.4",
"protein_coding": true,
"protein_id": "ENSP00000301067.7",
"strand": false,
"transcript": "ENST00000301067.12",
"transcript_support_level": 5
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 5553,
"aa_ref": "P",
"aa_start": 2390,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 20686,
"cdna_start": 8389,
"cds_end": null,
"cds_length": 16662,
"cds_start": 7170,
"consequences": [
"synonymous_variant"
],
"exon_count": 56,
"exon_rank": 32,
"exon_rank_end": null,
"feature": "ENST00000683543.2",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.7170G>A",
"hgvs_p": "p.Pro2390Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000506726.1",
"strand": false,
"transcript": "ENST00000683543.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 5540,
"aa_ref": "P",
"aa_start": 2393,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 16623,
"cdna_start": 7179,
"cds_end": null,
"cds_length": 16623,
"cds_start": 7179,
"consequences": [
"synonymous_variant"
],
"exon_count": 54,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000685166.1",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.7179G>A",
"hgvs_p": "p.Pro2393Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000509386.1",
"strand": false,
"transcript": "ENST00000685166.1",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 5536,
"aa_ref": "P",
"aa_start": 2389,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 16611,
"cdna_start": 7167,
"cds_end": null,
"cds_length": 16611,
"cds_start": 7167,
"consequences": [
"synonymous_variant"
],
"exon_count": 54,
"exon_rank": 31,
"exon_rank_end": null,
"feature": "ENST00000692637.1",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.7167G>A",
"hgvs_p": "p.Pro2389Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000509666.1",
"strand": false,
"transcript": "ENST00000692637.1",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 823,
"aa_ref": "P",
"aa_start": 426,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2475,
"cdna_start": 1279,
"cds_end": null,
"cds_length": 2474,
"cds_start": 1278,
"consequences": [
"synonymous_variant"
],
"exon_count": 6,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000689944.1",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.1278G>A",
"hgvs_p": "p.Pro426Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508812.1",
"strand": false,
"transcript": "ENST00000689944.1",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 793,
"aa_ref": "P",
"aa_start": 396,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2385,
"cdna_start": 1189,
"cds_end": null,
"cds_length": 2384,
"cds_start": 1188,
"consequences": [
"synonymous_variant"
],
"exon_count": 6,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000689060.1",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "c.1188G>A",
"hgvs_p": "p.Pro396Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000509018.1",
"strand": false,
"transcript": "ENST00000689060.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3958,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 5,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000689143.1",
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"hgvs_c": "n.843G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000509839.1",
"strand": false,
"transcript": "ENST00000689143.1",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs3741625",
"effect": "synonymous_variant",
"frequency_reference_population": 0.000058985253,
"gene_hgnc_id": 7133,
"gene_symbol": "KMT2D",
"gnomad_exomes_ac": 88,
"gnomad_exomes_af": 0.0000602285,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_ac": 7,
"gnomad_genomes_af": 0.0000468321,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"phenotype_combined": "Kabuki syndrome 1|Kabuki syndrome",
"phylop100way_prediction": "Benign",
"phylop100way_score": 0.471,
"pos": 49040600,
"ref": "C",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_003482.4"
}
]
}