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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: 10-99879821-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=99879821&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 99879821,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_015221.4",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "NM_015221.4",
"protein_id": "NP_056036.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 4658,
"cdna_end": null,
"cdna_length": 6428,
"mane_select": "ENST00000324109.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015221.4"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "ENST00000324109.9",
"protein_id": "ENSP00000315659.4",
"transcript_support_level": 1,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 4658,
"cdna_end": null,
"cdna_length": 6428,
"mane_select": "NM_015221.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000324109.9"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.2402A>G",
"hgvs_p": "p.Glu801Gly",
"transcript": "ENST00000543621.6",
"protein_id": "ENSP00000443657.2",
"transcript_support_level": 1,
"aa_start": 801,
"aa_end": null,
"aa_length": 865,
"cds_start": 2402,
"cds_end": null,
"cds_length": 2598,
"cdna_start": 2408,
"cdna_end": null,
"cdna_length": 4178,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000543621.6"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "NM_001441287.1",
"protein_id": "NP_001428216.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 4740,
"cdna_end": null,
"cdna_length": 6510,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441287.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "ENST00000856964.1",
"protein_id": "ENSP00000527023.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 4736,
"cdna_end": null,
"cdna_length": 6506,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000856964.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "ENST00000928782.1",
"protein_id": "ENSP00000598841.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 4824,
"cdna_end": null,
"cdna_length": 6592,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928782.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4409A>G",
"hgvs_p": "p.Glu1470Gly",
"transcript": "NM_001441288.1",
"protein_id": "NP_001428217.1",
"transcript_support_level": null,
"aa_start": 1470,
"aa_end": null,
"aa_length": 1534,
"cds_start": 4409,
"cds_end": null,
"cds_length": 4605,
"cdna_start": 4529,
"cdna_end": null,
"cdna_length": 6299,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441288.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4409A>G",
"hgvs_p": "p.Glu1470Gly",
"transcript": "ENST00000856965.1",
"protein_id": "ENSP00000527024.1",
"transcript_support_level": null,
"aa_start": 1470,
"aa_end": null,
"aa_length": 1534,
"cds_start": 4409,
"cds_end": null,
"cds_length": 4605,
"cdna_start": 4495,
"cdna_end": null,
"cdna_length": 6264,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000856965.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.3434A>G",
"hgvs_p": "p.Glu1145Gly",
"transcript": "NM_001318326.2",
"protein_id": "NP_001305255.1",
"transcript_support_level": null,
"aa_start": 1145,
"aa_end": null,
"aa_length": 1209,
"cds_start": 3434,
"cds_end": null,
"cds_length": 3630,
"cdna_start": 3578,
"cdna_end": null,
"cdna_length": 5348,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318326.2"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.3434A>G",
"hgvs_p": "p.Glu1145Gly",
"transcript": "ENST00000636706.1",
"protein_id": "ENSP00000489875.1",
"transcript_support_level": 2,
"aa_start": 1145,
"aa_end": null,
"aa_length": 1209,
"cds_start": 3434,
"cds_end": null,
"cds_length": 3630,
"cdna_start": 3667,
"cdna_end": null,
"cdna_length": 5437,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000636706.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.2276A>G",
"hgvs_p": "p.Glu759Gly",
"transcript": "NM_001318327.2",
"protein_id": "NP_001305256.2",
"transcript_support_level": null,
"aa_start": 759,
"aa_end": null,
"aa_length": 823,
"cds_start": 2276,
"cds_end": null,
"cds_length": 2472,
"cdna_start": 2362,
"cdna_end": null,
"cdna_length": 4132,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318327.2"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.2273A>G",
"hgvs_p": "p.Glu758Gly",
"transcript": "NM_001441290.1",
"protein_id": "NP_001428219.1",
"transcript_support_level": null,
"aa_start": 758,
"aa_end": null,
"aa_length": 822,
"cds_start": 2273,
"cds_end": null,
"cds_length": 2469,
"cdna_start": 2359,
"cdna_end": null,
"cdna_length": 4129,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441290.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.2048A>G",
"hgvs_p": "p.Glu683Gly",
"transcript": "NM_001441291.1",
"protein_id": "NP_001428220.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 747,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2244,
"cdna_start": 2693,
"cdna_end": null,
"cdna_length": 4463,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441291.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.1760A>G",
"hgvs_p": "p.Glu587Gly",
"transcript": "NM_001441292.1",
"protein_id": "NP_001428221.1",
"transcript_support_level": null,
"aa_start": 587,
"aa_end": null,
"aa_length": 651,
"cds_start": 1760,
"cds_end": null,
"cds_length": 1956,
"cdna_start": 2262,
"cdna_end": null,
"cdna_length": 4032,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441292.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.1346A>G",
"hgvs_p": "p.Glu449Gly",
"transcript": "NM_001441293.1",
"protein_id": "NP_001428222.1",
"transcript_support_level": null,
"aa_start": 449,
"aa_end": null,
"aa_length": 513,
"cds_start": 1346,
"cds_end": null,
"cds_length": 1542,
"cdna_start": 2463,
"cdna_end": null,
"cdna_length": 4233,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001441293.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly",
"transcript": "XM_047424910.1",
"protein_id": "XP_047280866.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1577,
"cds_start": 4538,
"cds_end": null,
"cds_length": 4734,
"cdna_start": 7977,
"cdna_end": null,
"cdna_length": 9753,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047424910.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "n.4756A>G",
"hgvs_p": null,
"transcript": "NR_199816.1",
"protein_id": null,
"transcript_support_level": null,
"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": 6526,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_199816.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"hgvs_c": "n.2460A>G",
"hgvs_p": null,
"transcript": "NR_199817.1",
"protein_id": null,
"transcript_support_level": null,
"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": 4230,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_199817.1"
}
],
"gene_symbol": "DNMBP",
"gene_hgnc_id": 30373,
"dbsnp": "rs760025415",
"frequency_reference_population": 0.0000061960327,
"hom_count_reference_population": 0,
"allele_count_reference_population": 10,
"gnomad_exomes_af": 0.00000547306,
"gnomad_genomes_af": 0.000013138,
"gnomad_exomes_ac": 8,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.11935457587242126,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.035,
"revel_prediction": "Benign",
"alphamissense_score": 0.0898,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.39,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.397,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_015221.4",
"gene_symbol": "DNMBP",
"hgnc_id": 30373,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.4538A>G",
"hgvs_p": "p.Glu1513Gly"
}
],
"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
}