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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: 7-2256945-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=2256945&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 2256945,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_013321.4",
"consequences": [
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1213C>G",
"hgvs_p": "p.His405Asp",
"transcript": "NM_013321.4",
"protein_id": "NP_037453.1",
"transcript_support_level": null,
"aa_start": 405,
"aa_end": null,
"aa_length": 465,
"cds_start": 1213,
"cds_end": null,
"cds_length": 1398,
"cdna_start": 1233,
"cdna_end": null,
"cdna_length": 4704,
"mane_select": "ENST00000222990.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_013321.4"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1213C>G",
"hgvs_p": "p.His405Asp",
"transcript": "ENST00000222990.8",
"protein_id": "ENSP00000222990.3",
"transcript_support_level": 1,
"aa_start": 405,
"aa_end": null,
"aa_length": 465,
"cds_start": 1213,
"cds_end": null,
"cds_length": 1398,
"cdna_start": 1233,
"cdna_end": null,
"cdna_length": 4704,
"mane_select": "NM_013321.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000222990.8"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1210C>G",
"hgvs_p": "p.His404Asp",
"transcript": "ENST00000926983.1",
"protein_id": "ENSP00000597042.1",
"transcript_support_level": null,
"aa_start": 404,
"aa_end": null,
"aa_length": 464,
"cds_start": 1210,
"cds_end": null,
"cds_length": 1395,
"cdna_start": 1256,
"cdna_end": null,
"cdna_length": 1499,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926983.1"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1204C>G",
"hgvs_p": "p.His402Asp",
"transcript": "ENST00000878404.1",
"protein_id": "ENSP00000548463.1",
"transcript_support_level": null,
"aa_start": 402,
"aa_end": null,
"aa_length": 462,
"cds_start": 1204,
"cds_end": null,
"cds_length": 1389,
"cdna_start": 1214,
"cdna_end": null,
"cdna_length": 1449,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878404.1"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1132C>G",
"hgvs_p": "p.His378Asp",
"transcript": "ENST00000878403.1",
"protein_id": "ENSP00000548462.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 438,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1317,
"cdna_start": 1152,
"cdna_end": null,
"cdna_length": 1387,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878403.1"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.889C>G",
"hgvs_p": "p.His297Asp",
"transcript": "ENST00000926984.1",
"protein_id": "ENSP00000597043.1",
"transcript_support_level": null,
"aa_start": 297,
"aa_end": null,
"aa_length": 357,
"cds_start": 889,
"cds_end": null,
"cds_length": 1074,
"cdna_start": 891,
"cdna_end": null,
"cdna_length": 1129,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926984.1"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1189C>G",
"hgvs_p": "p.His397Asp",
"transcript": "XM_011515329.3",
"protein_id": "XP_011513631.1",
"transcript_support_level": null,
"aa_start": 397,
"aa_end": null,
"aa_length": 457,
"cds_start": 1189,
"cds_end": null,
"cds_length": 1374,
"cdna_start": 1386,
"cdna_end": null,
"cdna_length": 4857,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011515329.3"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1171C>G",
"hgvs_p": "p.His391Asp",
"transcript": "XM_011515330.3",
"protein_id": "XP_011513632.1",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 451,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1356,
"cdna_start": 1271,
"cdna_end": null,
"cdna_length": 4742,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011515330.3"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1054C>G",
"hgvs_p": "p.His352Asp",
"transcript": "XM_017012084.3",
"protein_id": "XP_016867573.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 412,
"cds_start": 1054,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 1395,
"cdna_end": null,
"cdna_length": 4866,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017012084.3"
},
{
"aa_ref": "H",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "c.1054C>G",
"hgvs_p": "p.His352Asp",
"transcript": "XM_047420281.1",
"protein_id": "XP_047276237.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 412,
"cds_start": 1054,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 1140,
"cdna_end": null,
"cdna_length": 4611,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420281.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"hgvs_c": "n.333C>G",
"hgvs_p": null,
"transcript": "ENST00000480807.1",
"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": 534,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000480807.1"
}
],
"gene_symbol": "SNX8",
"gene_hgnc_id": 14972,
"dbsnp": "rs1562419133",
"frequency_reference_population": 6.843362e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84336e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8022071123123169,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05999999865889549,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.207,
"revel_prediction": "Benign",
"alphamissense_score": 0.4981,
"alphamissense_prediction": "Uncertain_significance",
"bayesdelnoaf_score": 0.01,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 7.344,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.06,
"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_013321.4",
"gene_symbol": "SNX8",
"hgnc_id": 14972,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1213C>G",
"hgvs_p": "p.His405Asp"
}
],
"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
}