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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: 15-31038077-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=31038077&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 31038077,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000256552.11",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2406T>C",
"hgvs_p": "p.Asn802Asn",
"transcript": "NM_001252024.2",
"protein_id": "NP_001238953.1",
"transcript_support_level": null,
"aa_start": 802,
"aa_end": null,
"aa_length": 1625,
"cds_start": 2406,
"cds_end": null,
"cds_length": 4878,
"cdna_start": 2558,
"cdna_end": null,
"cdna_length": 5787,
"mane_select": "ENST00000256552.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2406T>C",
"hgvs_p": "p.Asn802Asn",
"transcript": "ENST00000256552.11",
"protein_id": "ENSP00000256552.7",
"transcript_support_level": 1,
"aa_start": 802,
"aa_end": null,
"aa_length": 1625,
"cds_start": 2406,
"cds_end": null,
"cds_length": 4878,
"cdna_start": 2558,
"cdna_end": null,
"cdna_length": 5787,
"mane_select": "NM_001252024.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2457T>C",
"hgvs_p": "p.Asn819Asn",
"transcript": "ENST00000558445.6",
"protein_id": "ENSP00000452946.2",
"transcript_support_level": 1,
"aa_start": 819,
"aa_end": null,
"aa_length": 1642,
"cds_start": 2457,
"cds_end": null,
"cds_length": 4929,
"cdna_start": 2658,
"cdna_end": null,
"cdna_length": 5887,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2340T>C",
"hgvs_p": "p.Asn780Asn",
"transcript": "ENST00000397795.7",
"protein_id": "ENSP00000380897.2",
"transcript_support_level": 1,
"aa_start": 780,
"aa_end": null,
"aa_length": 1603,
"cds_start": 2340,
"cds_end": null,
"cds_length": 4812,
"cdna_start": 2472,
"cdna_end": null,
"cdna_length": 5701,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2109T>C",
"hgvs_p": "p.Asn703Asn",
"transcript": "ENST00000558768.5",
"protein_id": "ENSP00000453119.2",
"transcript_support_level": 1,
"aa_start": 703,
"aa_end": null,
"aa_length": 1526,
"cds_start": 2109,
"cds_end": null,
"cds_length": 4581,
"cdna_start": 2109,
"cdna_end": null,
"cdna_length": 4581,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "n.*1467T>C",
"hgvs_p": null,
"transcript": "ENST00000560801.5",
"protein_id": "ENSP00000453644.2",
"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": 4454,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "n.*1467T>C",
"hgvs_p": null,
"transcript": "ENST00000560801.5",
"protein_id": "ENSP00000453644.2",
"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": 4454,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2457T>C",
"hgvs_p": "p.Asn819Asn",
"transcript": "NM_001252020.2",
"protein_id": "NP_001238949.1",
"transcript_support_level": null,
"aa_start": 819,
"aa_end": null,
"aa_length": 1642,
"cds_start": 2457,
"cds_end": null,
"cds_length": 4929,
"cdna_start": 2658,
"cdna_end": null,
"cdna_length": 5887,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2340T>C",
"hgvs_p": "p.Asn780Asn",
"transcript": "ENST00000711434.1",
"protein_id": "ENSP00000518752.1",
"transcript_support_level": null,
"aa_start": 780,
"aa_end": null,
"aa_length": 1609,
"cds_start": 2340,
"cds_end": null,
"cds_length": 4830,
"cdna_start": 2472,
"cdna_end": null,
"cdna_length": 5719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.2340T>C",
"hgvs_p": "p.Asn780Asn",
"transcript": "NM_002420.6",
"protein_id": "NP_002411.3",
"transcript_support_level": null,
"aa_start": 780,
"aa_end": null,
"aa_length": 1603,
"cds_start": 2340,
"cds_end": null,
"cds_length": 4812,
"cdna_start": 2472,
"cdna_end": null,
"cdna_length": 5701,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"hgvs_c": "c.545-9601T>C",
"hgvs_p": null,
"transcript": "ENST00000559177.6",
"protein_id": "ENSP00000453477.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 757,
"cds_start": -4,
"cds_end": null,
"cds_length": 2274,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2274,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ENSG00000259720",
"gene_hgnc_id": 58477,
"hgvs_c": "n.188+2155A>G",
"hgvs_p": null,
"transcript": "ENST00000561299.1",
"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": 263,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "TRPM1",
"gene_hgnc_id": 7146,
"dbsnp": "rs2288242",
"frequency_reference_population": 0.82236123,
"hom_count_reference_population": 549038,
"allele_count_reference_population": 1327143,
"gnomad_exomes_af": 0.82658,
"gnomad_genomes_af": 0.781846,
"gnomad_exomes_ac": 1208157,
"gnomad_genomes_ac": 118986,
"gnomad_exomes_homalt": 501828,
"gnomad_genomes_homalt": 47210,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8700000047683716,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.87,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.733,
"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": -21,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
"acmg_by_gene": [
{
"score": -21,
"benign_score": 21,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000256552.11",
"gene_symbol": "TRPM1",
"hgnc_id": 7146,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.2406T>C",
"hgvs_p": "p.Asn802Asn"
},
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000561299.1",
"gene_symbol": "ENSG00000259720",
"hgnc_id": 58477,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.188+2155A>G",
"hgvs_p": null
}
],
"clinvar_disease": "Congenital stationary night blindness 1C,not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:5",
"phenotype_combined": "Congenital stationary night blindness 1C|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}