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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: 11-61774107-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=61774107&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM2",
"PP3"
],
"effects": [
"missense_variant"
],
"gene_symbol": "MYRF",
"hgnc_id": 1181,
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"inheritance_mode": "AD,Unknown",
"pathogenic_score": 3,
"score": 3,
"transcript": "NM_001127392.3",
"verdict": "Uncertain_significance"
},
{
"benign_score": 0,
"criteria": [
"PM2",
"PP3"
],
"effects": [
"non_coding_transcript_exon_variant"
],
"gene_symbol": "TMEM258",
"hgnc_id": 1164,
"hgvs_c": "n.520G>A",
"hgvs_p": null,
"inheritance_mode": "AR",
"pathogenic_score": 3,
"score": 3,
"transcript": "ENST00000535042.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_score": 3,
"allele_count_reference_population": 4,
"alphamissense_prediction": null,
"alphamissense_score": 0.3269,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.11,
"chr": "11",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "Prostate cancer",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.8087129592895508,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1151,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5940,
"cdna_start": 1365,
"cds_end": null,
"cds_length": 3456,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_001127392.3",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000278836.10",
"protein_coding": true,
"protein_id": "NP_001120864.1",
"strand": true,
"transcript": "NM_001127392.3",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1151,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5940,
"cdna_start": 1365,
"cds_end": null,
"cds_length": 3456,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000278836.10",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001127392.3",
"protein_coding": true,
"protein_id": "ENSP00000278836.4",
"strand": true,
"transcript": "ENST00000278836.10",
"transcript_support_level": 1
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1111,
"aa_ref": "T",
"aa_start": 410,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5745,
"cdna_start": 1264,
"cds_end": null,
"cds_length": 3336,
"cds_start": 1229,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000265460.9",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1229C>T",
"hgvs_p": "p.Thr410Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000265460.5",
"strand": true,
"transcript": "ENST00000265460.9",
"transcript_support_level": 1
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1152,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5920,
"cdna_start": 1342,
"cds_end": null,
"cds_length": 3459,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856811.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526870.1",
"strand": true,
"transcript": "ENST00000856811.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1147,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5934,
"cdna_start": 1371,
"cds_end": null,
"cds_length": 3444,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856806.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526865.1",
"strand": true,
"transcript": "ENST00000856806.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1146,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5943,
"cdna_start": 1383,
"cds_end": null,
"cds_length": 3441,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856800.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526859.1",
"strand": true,
"transcript": "ENST00000856800.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1125,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5905,
"cdna_start": 1408,
"cds_end": null,
"cds_length": 3378,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856799.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526858.1",
"strand": true,
"transcript": "ENST00000856799.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1124,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5836,
"cdna_start": 1342,
"cds_end": null,
"cds_length": 3375,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856812.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526871.1",
"strand": true,
"transcript": "ENST00000856812.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1120,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5857,
"cdna_start": 1375,
"cds_end": null,
"cds_length": 3363,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856803.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526862.1",
"strand": true,
"transcript": "ENST00000856803.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1119,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5862,
"cdna_start": 1383,
"cds_end": null,
"cds_length": 3360,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856801.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526860.1",
"strand": true,
"transcript": "ENST00000856801.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1112,
"aa_ref": "T",
"aa_start": 400,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5823,
"cdna_start": 1308,
"cds_end": null,
"cds_length": 3339,
"cds_start": 1199,
"consequences": [
"missense_variant"
],
"exon_count": 28,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000856808.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1199C>T",
"hgvs_p": "p.Thr400Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526867.1",
"strand": true,
"transcript": "ENST00000856808.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1111,
"aa_ref": "T",
"aa_start": 410,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5757,
"cdna_start": 1275,
"cds_end": null,
"cds_length": 3336,
"cds_start": 1229,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NM_013279.4",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1229C>T",
"hgvs_p": "p.Thr410Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_037411.1",
"strand": true,
"transcript": "NM_013279.4",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1109,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5805,
"cdna_start": 1359,
"cds_end": null,
"cds_length": 3330,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856810.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526869.1",
"strand": true,
"transcript": "ENST00000856810.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1108,
"aa_ref": "T",
"aa_start": 419,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5843,
"cdna_start": 1402,
"cds_end": null,
"cds_length": 3327,
"cds_start": 1256,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000918479.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1256C>T",
"hgvs_p": "p.Thr419Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000588538.1",
"strand": true,
"transcript": "ENST00000918479.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1096,
"aa_ref": "T",
"aa_start": 368,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5783,
"cdna_start": 1222,
"cds_end": null,
"cds_length": 3291,
"cds_start": 1103,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856804.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1103C>T",
"hgvs_p": "p.Thr368Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526863.1",
"strand": true,
"transcript": "ENST00000856804.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1095,
"aa_ref": "T",
"aa_start": 368,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5815,
"cdna_start": 1255,
"cds_end": null,
"cds_length": 3288,
"cds_start": 1103,
"consequences": [
"missense_variant"
],
"exon_count": 27,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856798.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1103C>T",
"hgvs_p": "p.Thr368Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526857.1",
"strand": true,
"transcript": "ENST00000856798.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1069,
"aa_ref": "T",
"aa_start": 368,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5709,
"cdna_start": 1227,
"cds_end": null,
"cds_length": 3210,
"cds_start": 1103,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856802.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1103C>T",
"hgvs_p": "p.Thr368Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526861.1",
"strand": true,
"transcript": "ENST00000856802.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1068,
"aa_ref": "T",
"aa_start": 368,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5685,
"cdna_start": 1212,
"cds_end": null,
"cds_length": 3207,
"cds_start": 1103,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000856809.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1103C>T",
"hgvs_p": "p.Thr368Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526868.1",
"strand": true,
"transcript": "ENST00000856809.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1057,
"aa_ref": "T",
"aa_start": 368,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5694,
"cdna_start": 1255,
"cds_end": null,
"cds_length": 3174,
"cds_start": 1103,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000918478.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.1103C>T",
"hgvs_p": "p.Thr368Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000588537.1",
"strand": true,
"transcript": "ENST00000918478.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1032,
"aa_ref": "T",
"aa_start": 305,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5591,
"cdna_start": 1033,
"cds_end": null,
"cds_length": 3099,
"cds_start": 914,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000856805.1",
"gene_hgnc_id": 1181,
"gene_symbol": "MYRF",
"hgvs_c": "c.914C>T",
"hgvs_p": "p.Thr305Met",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000526864.1",
"strand": true,
"transcript": "ENST00000856805.1",
"transcript_support_level": null
},
{
"aa_alt": "M",
"aa_end": null,
"aa_length": 1021,
"aa_ref": "T",
"aa_start": 305,
"biotype": "protein_coding",
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}