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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: 7-5989930-TGG-CAA (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=5989930&ref=TGG&alt=CAA&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PP3"
],
"effects": [
"missense_variant"
],
"gene_symbol": "PMS2",
"hgnc_id": 9122,
"hgvs_c": "c.1198_1200delCCAinsTTG",
"hgvs_p": "p.Pro400Leu",
"inheritance_mode": "AR,AD",
"pathogenic_score": 1,
"score": 1,
"transcript": "NM_001406866.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PP3",
"acmg_score": 1,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "CAA",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "7",
"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": "L",
"aa_end": null,
"aa_length": 862,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5093,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2589,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_000535.7",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 862,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5093,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2589,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000265849.12",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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.804-6941_804-6939delCCAinsTTG",
"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": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000406569.8",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "n.1012_1014delCCAinsTTG",
"hgvs_p": null,
"intron_rank": null,
"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.63-7027_63-7025delCCAinsTTG",
"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": "L",
"aa_end": null,
"aa_length": 924,
"aa_ref": "P",
"aa_start": 400,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5279,
"cdna_start": 1230,
"cds_end": null,
"cds_length": 2775,
"cds_start": 1198,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406866.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1198_1200delCCAinsTTG",
"hgvs_p": "p.Pro400Leu",
"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": "L",
"aa_end": null,
"aa_length": 924,
"aa_ref": "P",
"aa_start": 400,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3597,
"cdna_start": 1265,
"cds_end": null,
"cds_length": 2775,
"cds_start": 1198,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699839.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1198_1200delCCAinsTTG",
"hgvs_p": "p.Pro400Leu",
"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": "L",
"aa_end": null,
"aa_length": 873,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5126,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2622,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001322014.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 873,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5167,
"cdna_start": 1117,
"cds_end": null,
"cds_length": 2622,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699766.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 870,
"aa_ref": "P",
"aa_start": 346,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5117,
"cdna_start": 1068,
"cds_end": null,
"cds_length": 2613,
"cds_start": 1036,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406868.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1036_1038delCCAinsTTG",
"hgvs_p": "p.Pro346Leu",
"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": "L",
"aa_end": null,
"aa_length": 861,
"aa_ref": "P",
"aa_start": 337,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2812,
"cdna_start": 1079,
"cds_end": null,
"cds_length": 2586,
"cds_start": 1009,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699840.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1009_1011delCCAinsTTG",
"hgvs_p": "p.Pro337Leu",
"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": "L",
"aa_end": null,
"aa_length": 826,
"aa_ref": "P",
"aa_start": 302,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4985,
"cdna_start": 936,
"cds_end": null,
"cds_length": 2481,
"cds_start": 904,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406869.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.904_906delCCAinsTTG",
"hgvs_p": "p.Pro302Leu",
"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": "L",
"aa_end": null,
"aa_length": 826,
"aa_ref": "P",
"aa_start": 302,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5035,
"cdna_start": 986,
"cds_end": null,
"cds_length": 2481,
"cds_start": 904,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699930.2",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.904_906delCCAinsTTG",
"hgvs_p": "p.Pro302Leu",
"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": "L",
"aa_end": null,
"aa_length": 814,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4949,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2445,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406871.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 814,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4990,
"cdna_start": 1117,
"cds_end": null,
"cds_length": 2445,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699768.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 806,
"aa_ref": "P",
"aa_start": 338,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4925,
"cdna_start": 1044,
"cds_end": null,
"cds_length": 2421,
"cds_start": 1012,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406872.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.1012_1014delCCAinsTTG",
"hgvs_p": "p.Pro338Leu",
"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": "L",
"aa_end": null,
"aa_length": 806,
"aa_ref": "P",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4925,
"cdna_start": 876,
"cds_end": null,
"cds_length": 2421,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406874.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.844_846delCCAinsTTG",
"hgvs_p": "p.Pro282Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393803.1",
"strand": false,
"transcript": "NM_001406874.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 806,
"aa_ref": "P",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2659,
"cdna_start": 926,
"cds_end": null,
"cds_length": 2421,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699827.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.844_846delCCAinsTTG",
"hgvs_p": "p.Pro282Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514628.1",
"strand": false,
"transcript": "ENST00000699827.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 796,
"aa_ref": "P",
"aa_start": 272,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4895,
"cdna_start": 846,
"cds_end": null,
"cds_length": 2391,
"cds_start": 814,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001406873.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.814_816delCCAinsTTG",
"hgvs_p": "p.Pro272Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001393802.1",
"strand": false,
"transcript": "NM_001406873.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 796,
"aa_ref": "P",
"aa_start": 272,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4880,
"cdna_start": 861,
"cds_end": null,
"cds_length": 2391,
"cds_start": 814,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000699754.1",
"gene_hgnc_id": 9122,
"gene_symbol": "PMS2",
"hgvs_c": "c.814_816delCCAinsTTG",
"hgvs_p": "p.Pro272Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000514563.1",
"strand": false,
"transcript": "ENST00000699754.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 770,
"aa_ref": "P",
"aa_start": 235,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5491,
"cdna_start": 1409,
"cds_end": null,
"cds_length": 2313,
"cds_start": 703,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": null,
"exon_rank_end": null,
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