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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: 12-55693282-GCC-CCG (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=55693282&ref=GCC&alt=CCG&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [],
"effects": [
"missense_variant"
],
"gene_symbol": "ITGA7",
"hgnc_id": 6143,
"hgvs_c": "c.2701_2703delGGCinsCGG",
"hgvs_p": "p.Gly901Arg",
"inheritance_mode": "AR,AD",
"pathogenic_score": 0,
"score": 0,
"transcript": "NM_001410977.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_score": 0,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "CCG",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "12",
"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": "R",
"aa_end": null,
"aa_length": 1137,
"aa_ref": "G",
"aa_start": 857,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4126,
"cdna_start": 2793,
"cds_end": null,
"cds_length": 3414,
"cds_start": 2569,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_002206.3",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2569_2571delGGCinsCGG",
"hgvs_p": "p.Gly857Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000257879.11",
"protein_coding": true,
"protein_id": "NP_002197.2",
"strand": false,
"transcript": "NM_002206.3",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1137,
"aa_ref": "G",
"aa_start": 857,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 4126,
"cdna_start": 2793,
"cds_end": null,
"cds_length": 3414,
"cds_start": 2569,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000257879.11",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2569_2571delGGCinsCGG",
"hgvs_p": "p.Gly857Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_002206.3",
"protein_coding": true,
"protein_id": "ENSP00000257879.7",
"strand": false,
"transcript": "ENST00000257879.11",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1141,
"aa_ref": "G",
"aa_start": 861,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4138,
"cdna_start": 2805,
"cds_end": null,
"cds_length": 3426,
"cds_start": 2581,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000553804.6",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2581_2583delGGCinsCGG",
"hgvs_p": "p.Gly861Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000452120.1",
"strand": false,
"transcript": "ENST00000553804.6",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1181,
"aa_ref": "G",
"aa_start": 901,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4258,
"cdna_start": 2925,
"cds_end": null,
"cds_length": 3546,
"cds_start": 2701,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001410977.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2701_2703delGGCinsCGG",
"hgvs_p": "p.Gly901Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001397906.1",
"strand": false,
"transcript": "NM_001410977.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1181,
"aa_ref": "G",
"aa_start": 901,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3930,
"cdna_start": 2732,
"cds_end": null,
"cds_length": 3546,
"cds_start": 2701,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000555728.5",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2701_2703delGGCinsCGG",
"hgvs_p": "p.Gly901Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000452387.1",
"strand": false,
"transcript": "ENST00000555728.5",
"transcript_support_level": 5
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1175,
"aa_ref": "G",
"aa_start": 895,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4238,
"cdna_start": 2905,
"cds_end": null,
"cds_length": 3528,
"cds_start": 2683,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888141.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2683_2685delGGCinsCGG",
"hgvs_p": "p.Gly895Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558199.1",
"strand": false,
"transcript": "ENST00000888141.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1170,
"aa_ref": "G",
"aa_start": 890,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4228,
"cdna_start": 2895,
"cds_end": null,
"cds_length": 3513,
"cds_start": 2668,
"consequences": [
"missense_variant"
],
"exon_count": 26,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888137.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2668_2670delGGCinsCGG",
"hgvs_p": "p.Gly890Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558196.1",
"strand": false,
"transcript": "ENST00000888137.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1148,
"aa_ref": "G",
"aa_start": 868,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4126,
"cdna_start": 2793,
"cds_end": null,
"cds_length": 3447,
"cds_start": 2602,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888151.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2602_2604delGGCinsCGG",
"hgvs_p": "p.Gly868Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558210.1",
"strand": false,
"transcript": "ENST00000888151.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1141,
"aa_ref": "G",
"aa_start": 861,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4138,
"cdna_start": 2805,
"cds_end": null,
"cds_length": 3426,
"cds_start": 2581,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001144996.2",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2581_2583delGGCinsCGG",
"hgvs_p": "p.Gly861Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001138468.1",
"strand": false,
"transcript": "NM_001144996.2",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1140,
"aa_ref": "G",
"aa_start": 861,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4105,
"cdna_start": 2775,
"cds_end": null,
"cds_length": 3423,
"cds_start": 2581,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888150.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2581_2583delGGCinsCGG",
"hgvs_p": "p.Gly861Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558209.1",
"strand": false,
"transcript": "ENST00000888150.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1136,
"aa_ref": "G",
"aa_start": 857,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4115,
"cdna_start": 2791,
"cds_end": null,
"cds_length": 3411,
"cds_start": 2569,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000945417.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2569_2571delGGCinsCGG",
"hgvs_p": "p.Gly857Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000615476.1",
"strand": false,
"transcript": "ENST00000945417.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1135,
"aa_ref": "G",
"aa_start": 855,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4120,
"cdna_start": 2787,
"cds_end": null,
"cds_length": 3408,
"cds_start": 2563,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001414029.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2563_2565delGGCinsCGG",
"hgvs_p": "p.Gly855Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001400958.1",
"strand": false,
"transcript": "NM_001414029.1",
"transcript_support_level": null
},
{
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"aa_length": 1135,
"aa_ref": "G",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4151,
"cdna_start": 2818,
"cds_end": null,
"cds_length": 3408,
"cds_start": 2563,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888129.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2563_2565delGGCinsCGG",
"hgvs_p": "p.Gly855Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558189.1",
"strand": false,
"transcript": "ENST00000888129.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1133,
"aa_ref": "G",
"aa_start": 853,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4117,
"cdna_start": 2784,
"cds_end": null,
"cds_length": 3402,
"cds_start": 2557,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888135.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2557_2559delGGCinsCGG",
"hgvs_p": "p.Gly853Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558193.1",
"strand": false,
"transcript": "ENST00000888135.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1131,
"aa_ref": "G",
"aa_start": 851,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4108,
"cdna_start": 2775,
"cds_end": null,
"cds_length": 3396,
"cds_start": 2551,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001374465.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2551_2553delGGCinsCGG",
"hgvs_p": "p.Gly851Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001361394.1",
"strand": false,
"transcript": "NM_001374465.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1131,
"aa_ref": "G",
"aa_start": 851,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4084,
"cdna_start": 2755,
"cds_end": null,
"cds_length": 3396,
"cds_start": 2551,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000347027.10",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2551_2553delGGCinsCGG",
"hgvs_p": "p.Gly851Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000343009.6",
"strand": false,
"transcript": "ENST00000347027.10",
"transcript_support_level": 5
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1130,
"aa_ref": "G",
"aa_start": 850,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4096,
"cdna_start": 2763,
"cds_end": null,
"cds_length": 3393,
"cds_start": 2548,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000888145.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2548_2550delGGCinsCGG",
"hgvs_p": "p.Gly850Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000558204.1",
"strand": false,
"transcript": "ENST00000888145.1",
"transcript_support_level": null
},
{
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"aa_end": null,
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"aa_ref": "G",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4006,
"cdna_start": 2679,
"cds_end": null,
"cds_length": 3390,
"cds_start": 2545,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000945420.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2545_2547delGGCinsCGG",
"hgvs_p": "p.Gly849Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000615479.1",
"strand": false,
"transcript": "ENST00000945420.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1128,
"aa_ref": "G",
"aa_start": 848,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4094,
"cdna_start": 2765,
"cds_end": null,
"cds_length": 3387,
"cds_start": 2542,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000945415.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2542_2544delGGCinsCGG",
"hgvs_p": "p.Gly848Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000615474.1",
"strand": false,
"transcript": "ENST00000945415.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1127,
"aa_ref": "G",
"aa_start": 847,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4096,
"cdna_start": 2763,
"cds_end": null,
"cds_length": 3384,
"cds_start": 2539,
"consequences": [
"missense_variant"
],
"exon_count": 25,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000912204.1",
"gene_hgnc_id": 6143,
"gene_symbol": "ITGA7",
"hgvs_c": "c.2539_2541delGGCinsCGG",
"hgvs_p": "p.Gly847Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000582263.1",
"strand": false,
"transcript": "ENST00000912204.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1126,
"aa_ref": "G",
"aa_start": 846,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4040,
"cdna_start": 2707,
"cds_end": null,
"cds_length": 3381,
"cds_start": 2536,
"consequences": [
"missense_variant"
],
"exon_count": 25,
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