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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: 14-24082562-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=24082562&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM2",
"PP2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "NRL",
"hgnc_id": 8002,
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"inheritance_mode": "AR,AD",
"pathogenic_score": 3,
"score": 3,
"transcript": "NM_006177.5",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP2",
"acmg_score": 3,
"allele_count_reference_population": 5,
"alphamissense_prediction": null,
"alphamissense_score": 0.0911,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.15,
"chr": "14",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "Retinal dystrophy,Retinitis pigmentosa 27,not provided",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"computational_prediction_selected": "Uncertain_significance",
"computational_score_selected": 0.5955268740653992,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3543,
"cdna_start": 542,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001354768.3",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000561028.6",
"protein_coding": true,
"protein_id": "NP_001341697.1",
"strand": false,
"transcript": "NM_001354768.3",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3543,
"cdna_start": 542,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000561028.6",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001354768.3",
"protein_coding": true,
"protein_id": "ENSP00000454062.2",
"strand": false,
"transcript": "ENST00000561028.6",
"transcript_support_level": 2
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1517,
"cdna_start": 731,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000396997.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000380193.1",
"strand": false,
"transcript": "ENST00000396997.1",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1976,
"cdna_start": 420,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000397002.6",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000380197.2",
"strand": false,
"transcript": "ENST00000397002.6",
"transcript_support_level": 1
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3708,
"cdna_start": 731,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001354769.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001341698.1",
"strand": false,
"transcript": "NM_001354769.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3731,
"cdna_start": 768,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_006177.5",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_006168.1",
"strand": false,
"transcript": "NM_006177.5",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2398,
"cdna_start": 895,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000905081.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575140.1",
"strand": false,
"transcript": "ENST00000905081.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1225,
"cdna_start": 403,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905082.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575141.1",
"strand": false,
"transcript": "ENST00000905082.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2200,
"cdna_start": 1378,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905083.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575142.1",
"strand": false,
"transcript": "ENST00000905083.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1236,
"cdna_start": 415,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000905084.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000575143.1",
"strand": false,
"transcript": "ENST00000905084.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1239,
"cdna_start": 417,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000933893.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000603952.1",
"strand": false,
"transcript": "ENST00000933893.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1187,
"cdna_start": 365,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 2,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000947384.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617443.1",
"strand": false,
"transcript": "ENST00000947384.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 339,
"aa_ref": "M",
"aa_start": 198,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3618,
"cdna_start": 617,
"cds_end": null,
"cds_length": 1020,
"cds_start": 593,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "XM_011536801.3",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.593T>C",
"hgvs_p": "p.Met198Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011535103.2",
"strand": false,
"transcript": "XM_011536801.3",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 237,
"aa_ref": "M",
"aa_start": 96,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3455,
"cdna_start": 454,
"cds_end": null,
"cds_length": 714,
"cds_start": 287,
"consequences": [
"missense_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "XM_011536805.3",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.287T>C",
"hgvs_p": "p.Met96Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011535107.1",
"strand": false,
"transcript": "XM_011536805.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 132,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3190,
"cdna_start": null,
"cds_end": null,
"cds_length": 399,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001354770.2",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.66+221T>C",
"hgvs_p": null,
"intron_rank": 2,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001341699.1",
"strand": false,
"transcript": "NM_001354770.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 234,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3303,
"cdna_start": null,
"cds_end": null,
"cds_length": 705,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_011536806.3",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.372+221T>C",
"hgvs_p": null,
"intron_rank": 2,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011535108.2",
"strand": false,
"transcript": "XM_011536806.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 64,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 737,
"cdna_start": null,
"cds_end": null,
"cds_length": 195,
"cds_start": null,
"consequences": [
"downstream_gene_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000558280.1",
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"hgvs_c": "c.*92T>C",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000454180.1",
"strand": true,
"transcript": "ENST00000558280.1",
"transcript_support_level": 5
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs397514516",
"effect": "missense_variant",
"frequency_reference_population": 0.0000034214986,
"gene_hgnc_id": 8002,
"gene_symbol": "NRL",
"gnomad_exomes_ac": 5,
"gnomad_exomes_af": 0.0000034215,
"gnomad_exomes_homalt": 0,
"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": "Uncertain significance",
"phenotype_combined": "Retinitis pigmentosa 27|Retinal dystrophy|not provided",
"phylop100way_prediction": "Benign",
"phylop100way_score": 2.067,
"pos": 24082562,
"ref": "A",
"revel_prediction": "Uncertain_significance",
"revel_score": 0.403,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_006177.5"
}
]
}