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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: 8-58585667-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=58585667&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "8",
"pos": 58585667,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001144772.1",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2644A>G",
"hgvs_p": "p.Ile882Val",
"transcript": "NM_003580.4",
"protein_id": "NP_003571.2",
"transcript_support_level": null,
"aa_start": 882,
"aa_end": null,
"aa_length": 917,
"cds_start": 2644,
"cds_end": null,
"cds_length": 2754,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000038176.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003580.4"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2644A>G",
"hgvs_p": "p.Ile882Val",
"transcript": "ENST00000038176.8",
"protein_id": "ENSP00000038176.3",
"transcript_support_level": 1,
"aa_start": 882,
"aa_end": null,
"aa_length": 917,
"cds_start": 2644,
"cds_end": null,
"cds_length": 2754,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003580.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000038176.8"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2737A>G",
"hgvs_p": "p.Ile913Val",
"transcript": "NM_001144772.1",
"protein_id": "NP_001138244.1",
"transcript_support_level": null,
"aa_start": 913,
"aa_end": null,
"aa_length": 948,
"cds_start": 2737,
"cds_end": null,
"cds_length": 2847,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001144772.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2737A>G",
"hgvs_p": "p.Ile913Val",
"transcript": "ENST00000427130.7",
"protein_id": "ENSP00000411012.2",
"transcript_support_level": 2,
"aa_start": 913,
"aa_end": null,
"aa_length": 948,
"cds_start": 2737,
"cds_end": null,
"cds_length": 2847,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000427130.7"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2713A>G",
"hgvs_p": "p.Ile905Val",
"transcript": "NM_001413006.1",
"protein_id": "NP_001399935.1",
"transcript_support_level": null,
"aa_start": 905,
"aa_end": null,
"aa_length": 940,
"cds_start": 2713,
"cds_end": null,
"cds_length": 2823,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413006.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2674A>G",
"hgvs_p": "p.Ile892Val",
"transcript": "ENST00000958102.1",
"protein_id": "ENSP00000628161.1",
"transcript_support_level": null,
"aa_start": 892,
"aa_end": null,
"aa_length": 927,
"cds_start": 2674,
"cds_end": null,
"cds_length": 2784,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958102.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2668A>G",
"hgvs_p": "p.Ile890Val",
"transcript": "NM_001412998.1",
"protein_id": "NP_001399927.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 925,
"cds_start": 2668,
"cds_end": null,
"cds_length": 2778,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412998.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2668A>G",
"hgvs_p": "p.Ile890Val",
"transcript": "ENST00000958106.1",
"protein_id": "ENSP00000628165.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 925,
"cds_start": 2668,
"cds_end": null,
"cds_length": 2778,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958106.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2665A>G",
"hgvs_p": "p.Ile889Val",
"transcript": "NM_001412994.1",
"protein_id": "NP_001399923.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 924,
"cds_start": 2665,
"cds_end": null,
"cds_length": 2775,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412994.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2665A>G",
"hgvs_p": "p.Ile889Val",
"transcript": "NM_001413005.1",
"protein_id": "NP_001399934.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 924,
"cds_start": 2665,
"cds_end": null,
"cds_length": 2775,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413005.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2665A>G",
"hgvs_p": "p.Ile889Val",
"transcript": "ENST00000870783.1",
"protein_id": "ENSP00000540842.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 924,
"cds_start": 2665,
"cds_end": null,
"cds_length": 2775,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000870783.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2665A>G",
"hgvs_p": "p.Ile889Val",
"transcript": "ENST00000958105.1",
"protein_id": "ENSP00000628164.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 924,
"cds_start": 2665,
"cds_end": null,
"cds_length": 2775,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958105.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2662A>G",
"hgvs_p": "p.Ile888Val",
"transcript": "NM_001412990.1",
"protein_id": "NP_001399919.1",
"transcript_support_level": null,
"aa_start": 888,
"aa_end": null,
"aa_length": 923,
"cds_start": 2662,
"cds_end": null,
"cds_length": 2772,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412990.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2662A>G",
"hgvs_p": "p.Ile888Val",
"transcript": "ENST00000958101.1",
"protein_id": "ENSP00000628160.1",
"transcript_support_level": null,
"aa_start": 888,
"aa_end": null,
"aa_length": 923,
"cds_start": 2662,
"cds_end": null,
"cds_length": 2772,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958101.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2653A>G",
"hgvs_p": "p.Ile885Val",
"transcript": "NM_001412992.1",
"protein_id": "NP_001399921.1",
"transcript_support_level": null,
"aa_start": 885,
"aa_end": null,
"aa_length": 920,
"cds_start": 2653,
"cds_end": null,
"cds_length": 2763,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412992.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2653A>G",
"hgvs_p": "p.Ile885Val",
"transcript": "ENST00000870782.1",
"protein_id": "ENSP00000540841.1",
"transcript_support_level": null,
"aa_start": 885,
"aa_end": null,
"aa_length": 920,
"cds_start": 2653,
"cds_end": null,
"cds_length": 2763,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000870782.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2647A>G",
"hgvs_p": "p.Ile883Val",
"transcript": "ENST00000958104.1",
"protein_id": "ENSP00000628163.1",
"transcript_support_level": null,
"aa_start": 883,
"aa_end": null,
"aa_length": 918,
"cds_start": 2647,
"cds_end": null,
"cds_length": 2757,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958104.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2641A>G",
"hgvs_p": "p.Ile881Val",
"transcript": "ENST00000958103.1",
"protein_id": "ENSP00000628162.1",
"transcript_support_level": null,
"aa_start": 881,
"aa_end": null,
"aa_length": 916,
"cds_start": 2641,
"cds_end": null,
"cds_length": 2751,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958103.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2578A>G",
"hgvs_p": "p.Ile860Val",
"transcript": "ENST00000870784.1",
"protein_id": "ENSP00000540843.1",
"transcript_support_level": null,
"aa_start": 860,
"aa_end": null,
"aa_length": 895,
"cds_start": 2578,
"cds_end": null,
"cds_length": 2688,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000870784.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2644A>G",
"hgvs_p": "p.Ile882Val",
"transcript": "NM_001412995.1",
"protein_id": "NP_001399924.1",
"transcript_support_level": null,
"aa_start": 882,
"aa_end": null,
"aa_length": 894,
"cds_start": 2644,
"cds_end": null,
"cds_length": 2685,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412995.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2254A>G",
"hgvs_p": "p.Ile752Val",
"transcript": "NM_001412991.1",
"protein_id": "NP_001399920.1",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 787,
"cds_start": 2254,
"cds_end": null,
"cds_length": 2364,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001412991.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NSMAF",
"gene_hgnc_id": 8017,
"hgvs_c": "c.2254A>G",
"hgvs_p": "p.Ile752Val",
"transcript": "NM_001412996.1",
"protein_id": "NP_001399925.1",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 787,
"cds_start": 2254,
"cds_end": null,
"cds_length": 2364,
"cdna_start": null,
"cdna_end": null,
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"phylop100way_score": 2.861,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001144772.1",
"gene_symbol": "NSMAF",
"hgnc_id": 8017,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2737A>G",
"hgvs_p": "p.Ile913Val"
}
],
"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
}