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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: 1-6475073-GAC-AAT (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=6475073&ref=GAC&alt=AAT&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [],
"effects": [
"missense_variant"
],
"gene_symbol": "PLEKHG5",
"hgnc_id": 29105,
"hgvs_c": "c.481_483delGTCinsATT",
"hgvs_p": "p.Val161Ile",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": 0,
"transcript": "NM_001265593.2",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_score": 0,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "AAT",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "1",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3580,
"cdna_start": 394,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_020631.6",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000377728.8",
"protein_coding": true,
"protein_id": "NP_065682.2",
"strand": false,
"transcript": "NM_020631.6",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3580,
"cdna_start": 394,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377728.8",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_020631.6",
"protein_coding": true,
"protein_id": "ENSP00000366957.3",
"strand": false,
"transcript": "ENST00000377728.8",
"transcript_support_level": 2
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1043,
"aa_ref": "V",
"aa_start": 129,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3753,
"cdna_start": 567,
"cds_end": null,
"cds_length": 3132,
"cds_start": 385,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377732.5",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.385_387delGTCinsATT",
"hgvs_p": "p.Val129Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000366961.1",
"strand": false,
"transcript": "ENST00000377732.5",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1043,
"aa_ref": "V",
"aa_start": 129,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3731,
"cdna_start": 545,
"cds_end": null,
"cds_length": 3132,
"cds_start": 385,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000400915.8",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.385_387delGTCinsATT",
"hgvs_p": "p.Val129Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000383706.4",
"strand": false,
"transcript": "ENST00000400915.8",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4191,
"cdna_start": 1005,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377740.5",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000366969.4",
"strand": false,
"transcript": "ENST00000377740.5",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 930,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3475,
"cdna_start": 489,
"cds_end": null,
"cds_length": 2793,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377725.5",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000366954.1",
"strand": false,
"transcript": "ENST00000377725.5",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1105,
"aa_ref": "V",
"aa_start": 191,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3759,
"cdna_start": 573,
"cds_end": null,
"cds_length": 3318,
"cds_start": 571,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000673471.2",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.571_573delGTCinsATT",
"hgvs_p": "p.Val191Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000500749.1",
"strand": false,
"transcript": "ENST00000673471.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1075,
"aa_ref": "V",
"aa_start": 161,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3693,
"cdna_start": 507,
"cds_end": null,
"cds_length": 3228,
"cds_start": 481,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001265593.2",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.481_483delGTCinsATT",
"hgvs_p": "p.Val161Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001252522.1",
"strand": false,
"transcript": "NM_001265593.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1075,
"aa_ref": "V",
"aa_start": 161,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3695,
"cdna_start": 509,
"cds_end": null,
"cds_length": 3228,
"cds_start": 481,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000535355.6",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.481_483delGTCinsATT",
"hgvs_p": "p.Val161Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000441445.1",
"strand": false,
"transcript": "ENST00000535355.6",
"transcript_support_level": 2
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1064,
"aa_ref": "V",
"aa_start": 150,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3689,
"cdna_start": 503,
"cds_end": null,
"cds_length": 3195,
"cds_start": 448,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000377748.6",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.448_450delGTCinsATT",
"hgvs_p": "p.Val150Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000366977.2",
"strand": false,
"transcript": "ENST00000377748.6",
"transcript_support_level": 2
},
{
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"aa_end": null,
"aa_length": 1043,
"aa_ref": "V",
"aa_start": 129,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3719,
"cdna_start": 533,
"cds_end": null,
"cds_length": 3132,
"cds_start": 385,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001042663.3",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.385_387delGTCinsATT",
"hgvs_p": "p.Val129Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001036128.2",
"strand": false,
"transcript": "NM_001042663.3",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1043,
"aa_ref": "V",
"aa_start": 129,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3899,
"cdna_start": 713,
"cds_end": null,
"cds_length": 3132,
"cds_start": 385,
"consequences": [
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],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001265592.2",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.385_387delGTCinsATT",
"hgvs_p": "p.Val129Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001252521.2",
"strand": false,
"transcript": "NM_001265592.2",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 1043,
"aa_ref": "V",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3381,
"cdna_start": 578,
"cds_end": null,
"cds_length": 3132,
"cds_start": 385,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000537245.6",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.385_387delGTCinsATT",
"hgvs_p": "p.Val129Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000439625.2",
"strand": false,
"transcript": "ENST00000537245.6",
"transcript_support_level": 2
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1019,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3727,
"cdna_start": 507,
"cds_end": null,
"cds_length": 3060,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000856967.1",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000527026.1",
"strand": false,
"transcript": "ENST00000856967.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3685,
"cdna_start": 499,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001042664.2",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001036129.1",
"strand": false,
"transcript": "NM_001042664.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3665,
"cdna_start": 479,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001042665.2",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001036130.1",
"strand": false,
"transcript": "NM_001042665.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4274,
"cdna_start": 1088,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_198681.4",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_941374.3",
"strand": false,
"transcript": "NM_198681.4",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3699,
"cdna_start": 513,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000340850.10",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000344570.5",
"strand": false,
"transcript": "ENST00000340850.10",
"transcript_support_level": 5
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3668,
"cdna_start": 482,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000400913.6",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000383704.1",
"strand": false,
"transcript": "ENST00000400913.6",
"transcript_support_level": 5
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3637,
"cdna_start": 457,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000675694.1",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
"hgvs_p": "p.Val92Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000501925.1",
"strand": false,
"transcript": "ENST00000675694.1",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 1006,
"aa_ref": "V",
"aa_start": 92,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3849,
"cdna_start": 663,
"cds_end": null,
"cds_length": 3021,
"cds_start": 274,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000856966.1",
"gene_hgnc_id": 29105,
"gene_symbol": "PLEKHG5",
"hgvs_c": "c.274_276delGTCinsATT",
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