← Back to variant description
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: 11-103152204-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=103152204&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 103152204,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000375735.7",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 90,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "NM_001080463.2",
"protein_id": "NP_001073932.1",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4314,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12945,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13704,
"mane_select": null,
"mane_plus": "ENST00000650373.2",
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 90,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "ENST00000650373.2",
"protein_id": "ENSP00000497174.1",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4314,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12945,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13704,
"mane_select": null,
"mane_plus": "NM_001080463.2",
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 89,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "NM_001377.3",
"protein_id": "NP_001368.2",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4307,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12924,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13683,
"mane_select": "ENST00000375735.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 89,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "ENST00000375735.7",
"protein_id": "ENSP00000364887.2",
"transcript_support_level": 1,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4307,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12924,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13683,
"mane_select": "NM_001377.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.2205+17785A>G",
"hgvs_p": null,
"transcript": "ENST00000334267.11",
"protein_id": "ENSP00000334021.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 920,
"cds_start": -4,
"cds_end": null,
"cds_length": 2763,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2984,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3033A>G",
"hgvs_p": "p.Leu1011Leu",
"transcript": "ENST00000648198.1",
"protein_id": "ENSP00000497329.1",
"transcript_support_level": null,
"aa_start": 1011,
"aa_end": null,
"aa_length": 1255,
"cds_start": 3033,
"cds_end": null,
"cds_length": 3768,
"cdna_start": 3198,
"cdna_end": null,
"cdna_length": 4528,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 89,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "XM_006718903.3",
"protein_id": "XP_006718966.1",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4300,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12903,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13662,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 88,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "XM_017018291.2",
"protein_id": "XP_016873780.1",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 4237,
"cds_start": 3015,
"cds_end": null,
"cds_length": 12714,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 13473,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 86,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.2397A>G",
"hgvs_p": "p.Leu799Leu",
"transcript": "XM_017018292.2",
"protein_id": "XP_016873781.1",
"transcript_support_level": null,
"aa_start": 799,
"aa_end": null,
"aa_length": 4101,
"cds_start": 2397,
"cds_end": null,
"cds_length": 12306,
"cdna_start": 2413,
"cdna_end": null,
"cdna_length": 12932,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu",
"transcript": "XM_017018293.2",
"protein_id": "XP_016873782.1",
"transcript_support_level": null,
"aa_start": 1005,
"aa_end": null,
"aa_length": 2485,
"cds_start": 3015,
"cds_end": null,
"cds_length": 7458,
"cdna_start": 3164,
"cdna_end": null,
"cdna_length": 7699,
"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": 20,
"exon_rank_end": null,
"exon_count": 51,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "n.*472A>G",
"hgvs_p": null,
"transcript": "ENST00000649323.1",
"protein_id": "ENSP00000497581.1",
"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": 8330,
"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": 20,
"exon_rank_end": null,
"exon_count": 51,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"hgvs_c": "n.*472A>G",
"hgvs_p": null,
"transcript": "ENST00000649323.1",
"protein_id": "ENSP00000497581.1",
"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": 8330,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "DYNC2H1",
"gene_hgnc_id": 2962,
"dbsnp": "rs201310509",
"frequency_reference_population": 0.0004039224,
"hom_count_reference_population": 1,
"allele_count_reference_population": 650,
"gnomad_exomes_af": 0.000317615,
"gnomad_genomes_af": 0.00123447,
"gnomad_exomes_ac": 463,
"gnomad_genomes_ac": 187,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.5099999904632568,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.51,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.834,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.02,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong,BP6,BP7",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000375735.7",
"gene_symbol": "DYNC2H1",
"hgnc_id": 2962,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.3015A>G",
"hgvs_p": "p.Leu1005Leu"
}
],
"clinvar_disease": "Jeune thoracic dystrophy,not provided,not specified",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:1 LB:2 B:1",
"phenotype_combined": "not specified|Jeune thoracic dystrophy|not provided",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}