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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: 2-203049905-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=203049905&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 203049905,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001378026.1",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "NM_001378026.1",
"protein_id": "NP_001364955.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2723,
"cds_start": 235,
"cds_end": null,
"cds_length": 8172,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 16349,
"mane_select": "ENST00000683969.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "ENST00000683969.1",
"protein_id": "ENSP00000508055.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2723,
"cds_start": 235,
"cds_end": null,
"cds_length": 8172,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 16349,
"mane_select": "NM_001378026.1",
"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": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.522G>T",
"hgvs_p": null,
"transcript": "ENST00000478884.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 1012,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "NM_001114132.2",
"protein_id": "NP_001107604.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2694,
"cds_start": 235,
"cds_end": null,
"cds_length": 8085,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 16262,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "ENST00000449802.5",
"protein_id": "ENSP00000399903.1",
"transcript_support_level": 5,
"aa_start": 79,
"aa_end": null,
"aa_length": 2694,
"cds_start": 235,
"cds_end": null,
"cds_length": 8085,
"cdna_start": 568,
"cdna_end": null,
"cdna_length": 10938,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "ENST00000682108.1",
"protein_id": "ENSP00000507379.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2655,
"cds_start": 235,
"cds_end": null,
"cds_length": 7968,
"cdna_start": 235,
"cdna_end": null,
"cdna_length": 7968,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "ENST00000683091.1",
"protein_id": "ENSP00000506951.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 137,
"cds_start": 235,
"cds_end": null,
"cds_length": 415,
"cdna_start": 532,
"cdna_end": null,
"cdna_length": 712,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_006712698.5",
"protein_id": "XP_006712761.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2736,
"cds_start": 235,
"cds_end": null,
"cds_length": 8211,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 8759,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_011511658.4",
"protein_id": "XP_011509960.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2736,
"cds_start": 235,
"cds_end": null,
"cds_length": 8211,
"cdna_start": 565,
"cdna_end": null,
"cdna_length": 8752,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_011511659.3",
"protein_id": "XP_011509961.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2736,
"cds_start": 235,
"cds_end": null,
"cds_length": 8211,
"cdna_start": 611,
"cdna_end": null,
"cdna_length": 8798,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_005246787.5",
"protein_id": "XP_005246844.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2707,
"cds_start": 235,
"cds_end": null,
"cds_length": 8124,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 8480,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_047445554.1",
"protein_id": "XP_047301510.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2707,
"cds_start": 235,
"cds_end": null,
"cds_length": 8124,
"cdna_start": 565,
"cdna_end": null,
"cdna_length": 8473,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 47,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser",
"transcript": "XM_011511663.4",
"protein_id": "XP_011509965.1",
"transcript_support_level": null,
"aa_start": 79,
"aa_end": null,
"aa_length": 2371,
"cds_start": 235,
"cds_end": null,
"cds_length": 7116,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 7673,
"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": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.255G>T",
"hgvs_p": null,
"transcript": "ENST00000460416.2",
"protein_id": null,
"transcript_support_level": 5,
"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": 518,
"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": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.579G>T",
"hgvs_p": null,
"transcript": "ENST00000463830.2",
"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": 2841,
"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": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.568G>T",
"hgvs_p": null,
"transcript": "ENST00000497505.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 2372,
"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": 3,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.235G>T",
"hgvs_p": null,
"transcript": "ENST00000681967.1",
"protein_id": "ENSP00000507195.1",
"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": 10523,
"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": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.579G>T",
"hgvs_p": null,
"transcript": "ENST00000682333.1",
"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": 2545,
"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": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.*156G>T",
"hgvs_p": null,
"transcript": "ENST00000682787.1",
"protein_id": "ENSP00000507858.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"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": 3,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.235G>T",
"hgvs_p": null,
"transcript": "ENST00000683001.1",
"protein_id": "ENSP00000507558.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7999,
"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": 3,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.235G>T",
"hgvs_p": null,
"transcript": "ENST00000683338.1",
"protein_id": "ENSP00000506761.1",
"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": 8201,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 51,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "c.-98G>T",
"hgvs_p": null,
"transcript": "XM_011511660.3",
"protein_id": "XP_011509962.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2598,
"cds_start": -4,
"cds_end": null,
"cds_length": 7797,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8115,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"hgvs_c": "n.*156G>T",
"hgvs_p": null,
"transcript": "ENST00000682787.1",
"protein_id": "ENSP00000507858.1",
"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": 856,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "NBEAL1",
"gene_hgnc_id": 20681,
"dbsnp": "rs1339041271",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": 0,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 0,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09525907039642334,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.082,
"revel_prediction": "Benign",
"alphamissense_score": 0.079,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.49,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.396,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.01,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001378026.1",
"gene_symbol": "NBEAL1",
"hgnc_id": 20681,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.235G>T",
"hgvs_p": "p.Ala79Ser"
}
],
"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
}