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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: 12-44523403-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=44523403&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 44523403,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001145107.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "NM_001145108.2",
"protein_id": "NP_001138580.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000429094.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001145108.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "ENST00000429094.7",
"protein_id": "ENSP00000390680.2",
"transcript_support_level": 1,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001145108.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000429094.7"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "ENST00000452445.6",
"protein_id": "ENSP00000394612.2",
"transcript_support_level": 1,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000452445.6"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1883G>C",
"hgvs_p": "p.Arg628Pro",
"transcript": "ENST00000395487.6",
"protein_id": "ENSP00000378866.2",
"transcript_support_level": 1,
"aa_start": 628,
"aa_end": null,
"aa_length": 815,
"cds_start": 1883,
"cds_end": null,
"cds_length": 2448,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000395487.6"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1742G>C",
"hgvs_p": "p.Arg581Pro",
"transcript": "ENST00000551601.5",
"protein_id": "ENSP00000449332.1",
"transcript_support_level": 1,
"aa_start": 581,
"aa_end": null,
"aa_length": 768,
"cds_start": 1742,
"cds_end": null,
"cds_length": 2307,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000551601.5"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.2036G>C",
"hgvs_p": "p.Arg679Pro",
"transcript": "NM_001145107.2",
"protein_id": "NP_001138579.1",
"transcript_support_level": null,
"aa_start": 679,
"aa_end": null,
"aa_length": 866,
"cds_start": 2036,
"cds_end": null,
"cds_length": 2601,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001145107.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.2036G>C",
"hgvs_p": "p.Arg679Pro",
"transcript": "ENST00000437801.6",
"protein_id": "ENSP00000416341.2",
"transcript_support_level": 2,
"aa_start": 679,
"aa_end": null,
"aa_length": 866,
"cds_start": 2036,
"cds_end": null,
"cds_length": 2601,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000437801.6"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1955G>C",
"hgvs_p": "p.Arg652Pro",
"transcript": "NM_001145110.2",
"protein_id": "NP_001138582.1",
"transcript_support_level": null,
"aa_start": 652,
"aa_end": null,
"aa_length": 839,
"cds_start": 1955,
"cds_end": null,
"cds_length": 2520,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001145110.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1955G>C",
"hgvs_p": "p.Arg652Pro",
"transcript": "ENST00000333837.8",
"protein_id": "ENSP00000327988.4",
"transcript_support_level": 2,
"aa_start": 652,
"aa_end": null,
"aa_length": 839,
"cds_start": 1955,
"cds_end": null,
"cds_length": 2520,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000333837.8"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "NM_006159.2",
"protein_id": "NP_006150.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006159.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "ENST00000868481.1",
"protein_id": "ENSP00000538540.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868481.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "ENST00000967237.1",
"protein_id": "ENSP00000637296.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967237.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1883G>C",
"hgvs_p": "p.Arg628Pro",
"transcript": "NM_001145109.2",
"protein_id": "NP_001138581.1",
"transcript_support_level": null,
"aa_start": 628,
"aa_end": null,
"aa_length": 815,
"cds_start": 1883,
"cds_end": null,
"cds_length": 2448,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001145109.2"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1883G>C",
"hgvs_p": "p.Arg628Pro",
"transcript": "ENST00000549027.5",
"protein_id": "ENSP00000447927.1",
"transcript_support_level": 5,
"aa_start": 628,
"aa_end": null,
"aa_length": 815,
"cds_start": 1883,
"cds_end": null,
"cds_length": 2448,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000549027.5"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1745G>C",
"hgvs_p": "p.Arg582Pro",
"transcript": "ENST00000967238.1",
"protein_id": "ENSP00000637297.1",
"transcript_support_level": null,
"aa_start": 582,
"aa_end": null,
"aa_length": 769,
"cds_start": 1745,
"cds_end": null,
"cds_length": 2310,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967238.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "ENST00000868482.1",
"protein_id": "ENSP00000538541.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 736,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2211,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868482.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1562G>C",
"hgvs_p": "p.Arg521Pro",
"transcript": "ENST00000967239.1",
"protein_id": "ENSP00000637298.1",
"transcript_support_level": null,
"aa_start": 521,
"aa_end": null,
"aa_length": 708,
"cds_start": 1562,
"cds_end": null,
"cds_length": 2127,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967239.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.122G>C",
"hgvs_p": "p.Arg41Pro",
"transcript": "ENST00000550139.1",
"protein_id": "ENSP00000448107.1",
"transcript_support_level": 3,
"aa_start": 41,
"aa_end": null,
"aa_length": 85,
"cds_start": 122,
"cds_end": null,
"cds_length": 258,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000550139.1"
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "c.1886G>C",
"hgvs_p": "p.Arg629Pro",
"transcript": "XM_011538396.2",
"protein_id": "XP_011536698.1",
"transcript_support_level": null,
"aa_start": 629,
"aa_end": null,
"aa_length": 816,
"cds_start": 1886,
"cds_end": null,
"cds_length": 2451,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538396.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"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": "NELL2",
"gene_hgnc_id": 7751,
"hgvs_c": "n.233G>C",
"hgvs_p": null,
"transcript": "ENST00000547636.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000547636.1"
}
],
"gene_symbol": "NELL2",
"gene_hgnc_id": 7751,
"dbsnp": "rs757288037",
"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": 0.7851426005363464,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.67,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9867,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.37,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 6.078,
"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": 3,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_by_gene": [
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001145107.2",
"gene_symbol": "NELL2",
"hgnc_id": 7751,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2036G>C",
"hgvs_p": "p.Arg679Pro"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}