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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: 7-100572715-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=100572715&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 100572715,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001348680.2",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.548C>T",
"hgvs_p": "p.Ser183Leu",
"transcript": "NM_001348680.2",
"protein_id": "NP_001335609.1",
"transcript_support_level": null,
"aa_start": 183,
"aa_end": null,
"aa_length": 297,
"cds_start": 548,
"cds_end": null,
"cds_length": 894,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1111,
"mane_select": "ENST00000622764.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.548C>T",
"hgvs_p": "p.Ser183Leu",
"transcript": "ENST00000622764.3",
"protein_id": "ENSP00000481773.2",
"transcript_support_level": 5,
"aa_start": 183,
"aa_end": null,
"aa_length": 297,
"cds_start": 548,
"cds_end": null,
"cds_length": 894,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1111,
"mane_select": "NM_001348680.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.527C>T",
"hgvs_p": "p.Ser176Leu",
"transcript": "NM_001168682.3",
"protein_id": "NP_001162153.2",
"transcript_support_level": null,
"aa_start": 176,
"aa_end": null,
"aa_length": 290,
"cds_start": 527,
"cds_end": null,
"cds_length": 873,
"cdna_start": 685,
"cdna_end": null,
"cdna_length": 1090,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.254C>T",
"hgvs_p": "p.Ser85Leu",
"transcript": "NM_001348677.2",
"protein_id": "NP_001335606.1",
"transcript_support_level": null,
"aa_start": 85,
"aa_end": null,
"aa_length": 199,
"cds_start": 254,
"cds_end": null,
"cds_length": 600,
"cdna_start": 902,
"cdna_end": null,
"cdna_length": 1307,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.254C>T",
"hgvs_p": "p.Ser85Leu",
"transcript": "ENST00000538735.5",
"protein_id": "ENSP00000442339.1",
"transcript_support_level": 3,
"aa_start": 85,
"aa_end": null,
"aa_length": 199,
"cds_start": 254,
"cds_end": null,
"cds_length": 600,
"cdna_start": 432,
"cdna_end": null,
"cdna_length": 837,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "c.254C>T",
"hgvs_p": "p.Ser85Leu",
"transcript": "ENST00000614631.4",
"protein_id": "ENSP00000481351.1",
"transcript_support_level": 2,
"aa_start": 85,
"aa_end": null,
"aa_length": 199,
"cds_start": 254,
"cds_end": null,
"cds_length": 600,
"cdna_start": 610,
"cdna_end": null,
"cdna_length": 987,
"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": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000274272",
"gene_hgnc_id": null,
"hgvs_c": "n.4000C>T",
"hgvs_p": null,
"transcript": "ENST00000485071.2",
"protein_id": null,
"transcript_support_level": 2,
"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": 4401,
"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": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"hgvs_c": "n.352C>T",
"hgvs_p": null,
"transcript": "ENST00000611464.1",
"protein_id": null,
"transcript_support_level": 2,
"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": 668,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SAP25",
"gene_hgnc_id": 41908,
"dbsnp": "rs556504446",
"frequency_reference_population": 0.00007617832,
"hom_count_reference_population": 0,
"allele_count_reference_population": 117,
"gnomad_exomes_af": 0.0000751533,
"gnomad_genomes_af": 0.0000855083,
"gnomad_exomes_ac": 104,
"gnomad_genomes_ac": 13,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.03456076979637146,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.031,
"revel_prediction": "Benign",
"alphamissense_score": 0.1002,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.56,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.105,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong,BP6_Moderate",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_001348680.2",
"gene_symbol": "SAP25",
"hgnc_id": 41908,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.548C>T",
"hgvs_p": "p.Ser183Leu"
},
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000485071.2",
"gene_symbol": "ENSG00000274272",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.4000C>T",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}