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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: 7-5986766-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=5986766&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 1,
"criteria": [
"PM2",
"BP4"
],
"effects": [
"missense_variant"
],
"gene_symbol": "PMS2",
"hgnc_id": 9122,
"hgvs_c": "c.2185G>C",
"hgvs_p": "p.Glu729Gln",
"inheritance_mode": "AR,AD",
"pathogenic_score": 2,
"score": 1,
"transcript": "NM_001406866.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_score": 1,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": 0.2727,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Uncertain_significance",
"bayesdelnoaf_score": -0.07,
"chr": "7",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "Hereditary cancer-predisposing syndrome,Hereditary nonpolyposis colorectal neoplasms",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.41645920276641846,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 862,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5093,
"cdna_start": 2029,
"cds_end": null,
"cds_length": 2589,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_000535.7",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000265849.12",
"protein_coding": true,
"protein_id": "NP_000526.2",
"strand": false,
"transcript": "NM_000535.7",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 862,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5093,
"cdna_start": 2029,
"cds_end": null,
"cds_length": 2589,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000265849.12",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000535.7",
"protein_coding": true,
"protein_id": "ENSP00000265849.7",
"strand": false,
"transcript": "ENST00000265849.12",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 461,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1386,
"cdna_start": null,
"cds_end": null,
"cds_length": 1386,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000382321.5",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.804-3775G>C",
"hgvs_p": null,
"intron_rank": 7,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000371758.4",
"strand": false,
"transcript": "ENST00000382321.5",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2101,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000406569.8",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "n.1678+321G>C",
"hgvs_p": null,
"intron_rank": 11,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000514464.1",
"strand": false,
"transcript": "ENST00000406569.8",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 93,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 3,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000469652.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "n.63-3861G>C",
"hgvs_p": null,
"intron_rank": 2,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000469652.1",
"transcript_support_level": 1
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 924,
"aa_ref": "E",
"aa_start": 729,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5279,
"cdna_start": 2215,
"cds_end": null,
"cds_length": 2775,
"cds_start": 2185,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001406866.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.2185G>C",
"hgvs_p": "p.Glu729Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393795.1",
"strand": false,
"transcript": "NM_001406866.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 924,
"aa_ref": "E",
"aa_start": 729,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3597,
"cdna_start": 2250,
"cds_end": null,
"cds_length": 2775,
"cds_start": 2185,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000699839.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.2185G>C",
"hgvs_p": "p.Glu729Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514637.1",
"strand": false,
"transcript": "ENST00000699839.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 873,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5126,
"cdna_start": 2029,
"cds_end": null,
"cds_length": 2622,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001322014.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001308943.1",
"strand": false,
"transcript": "NM_001322014.2",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 873,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5167,
"cdna_start": 2102,
"cds_end": null,
"cds_length": 2622,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000699766.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514574.1",
"strand": false,
"transcript": "ENST00000699766.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 870,
"aa_ref": "E",
"aa_start": 675,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5117,
"cdna_start": 2053,
"cds_end": null,
"cds_length": 2613,
"cds_start": 2023,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001406868.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.2023G>C",
"hgvs_p": "p.Glu675Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393797.1",
"strand": false,
"transcript": "NM_001406868.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 861,
"aa_ref": "E",
"aa_start": 666,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2812,
"cdna_start": 2064,
"cds_end": null,
"cds_length": 2586,
"cds_start": 1996,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000699840.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1996G>C",
"hgvs_p": "p.Glu666Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514638.2",
"strand": false,
"transcript": "ENST00000699840.2",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 826,
"aa_ref": "E",
"aa_start": 631,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4985,
"cdna_start": 1921,
"cds_end": null,
"cds_length": 2481,
"cds_start": 1891,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001406869.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1891G>C",
"hgvs_p": "p.Glu631Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393798.1",
"strand": false,
"transcript": "NM_001406869.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 826,
"aa_ref": "E",
"aa_start": 631,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5035,
"cdna_start": 1971,
"cds_end": null,
"cds_length": 2481,
"cds_start": 1891,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000699930.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1891G>C",
"hgvs_p": "p.Glu631Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514695.2",
"strand": false,
"transcript": "ENST00000699930.2",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 821,
"aa_ref": "E",
"aa_start": 615,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4970,
"cdna_start": 1873,
"cds_end": null,
"cds_length": 2466,
"cds_start": 1843,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001406870.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1843G>C",
"hgvs_p": "p.Glu615Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393799.1",
"strand": false,
"transcript": "NM_001406870.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 821,
"aa_ref": "E",
"aa_start": 615,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2616,
"cdna_start": 1865,
"cds_end": null,
"cds_length": 2466,
"cds_start": 1843,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000933314.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1843G>C",
"hgvs_p": "p.Glu615Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000603373.1",
"strand": false,
"transcript": "ENST00000933314.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 814,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4949,
"cdna_start": 2029,
"cds_end": null,
"cds_length": 2445,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001406871.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393800.1",
"strand": false,
"transcript": "NM_001406871.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 814,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4990,
"cdna_start": 2102,
"cds_end": null,
"cds_length": 2445,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000699768.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514576.1",
"strand": false,
"transcript": "ENST00000699768.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 810,
"aa_ref": "E",
"aa_start": 615,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4937,
"cdna_start": 1873,
"cds_end": null,
"cds_length": 2433,
"cds_start": 1843,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001322006.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1843G>C",
"hgvs_p": "p.Glu615Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001308935.1",
"strand": false,
"transcript": "NM_001322006.2",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 810,
"aa_ref": "E",
"aa_start": 615,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4907,
"cdna_start": 1873,
"cds_end": null,
"cds_length": 2433,
"cds_start": 1843,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000699752.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1843G>C",
"hgvs_p": "p.Glu615Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514561.1",
"strand": false,
"transcript": "ENST00000699752.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 806,
"aa_ref": "E",
"aa_start": 667,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4925,
"cdna_start": 2029,
"cds_end": null,
"cds_length": 2421,
"cds_start": 1999,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001406872.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1999G>C",
"hgvs_p": "p.Glu667Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393801.1",
"strand": false,
"transcript": "NM_001406872.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 806,
"aa_ref": "E",
"aa_start": 611,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4925,
"cdna_start": 1861,
"cds_end": null,
"cds_length": 2421,
"cds_start": 1831,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001406874.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
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