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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: 2-33524042-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=33524042&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 33524042,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_170672.3",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "NM_001139488.2",
"protein_id": "NP_001132960.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 999,
"cdna_end": null,
"cdna_length": 4386,
"mane_select": "ENST00000403687.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001139488.2"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000403687.8",
"protein_id": "ENSP00000384192.3",
"transcript_support_level": 1,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 999,
"cdna_end": null,
"cdna_length": 4386,
"mane_select": "NM_001139488.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000403687.8"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000402538.8",
"protein_id": "ENSP00000385886.3",
"transcript_support_level": 1,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1332,
"cdna_end": null,
"cdna_length": 6337,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402538.8"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000407811.5",
"protein_id": "ENSP00000383917.1",
"transcript_support_level": 1,
"aa_start": 227,
"aa_end": null,
"aa_length": 689,
"cds_start": 680,
"cds_end": null,
"cds_length": 2070,
"cdna_start": 952,
"cdna_end": null,
"cdna_length": 4210,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000407811.5"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000850562.1",
"protein_id": "ENSP00000520853.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 726,
"cds_start": 680,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 1002,
"cdna_end": null,
"cdna_length": 2683,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000850562.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000850563.1",
"protein_id": "ENSP00000520854.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 725,
"cds_start": 680,
"cds_end": null,
"cds_length": 2178,
"cdna_start": 999,
"cdna_end": null,
"cdna_length": 4156,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000850563.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000967278.1",
"protein_id": "ENSP00000637337.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 700,
"cds_start": 680,
"cds_end": null,
"cds_length": 2103,
"cdna_start": 1223,
"cdna_end": null,
"cdna_length": 2966,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967278.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "NM_001349975.2",
"protein_id": "NP_001336904.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1430,
"cdna_end": null,
"cdna_length": 4817,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349975.2"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "NM_001349976.2",
"protein_id": "NP_001336905.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 897,
"cdna_end": null,
"cdna_length": 4284,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349976.2"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "NM_001349977.2",
"protein_id": "NP_001336906.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1121,
"cdna_end": null,
"cdna_length": 4508,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349977.2"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "NM_170672.3",
"protein_id": "NP_733772.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1308,
"cdna_end": null,
"cdna_length": 4695,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_170672.3"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884676.1",
"protein_id": "ENSP00000554735.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1553,
"cdna_end": null,
"cdna_length": 4812,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884676.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884677.1",
"protein_id": "ENSP00000554736.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1508,
"cdna_end": null,
"cdna_length": 3854,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884677.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884679.1",
"protein_id": "ENSP00000554738.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1181,
"cdna_end": null,
"cdna_length": 5860,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884679.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884682.1",
"protein_id": "ENSP00000554741.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1173,
"cdna_end": null,
"cdna_length": 4436,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884682.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884683.1",
"protein_id": "ENSP00000554742.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1187,
"cdna_end": null,
"cdna_length": 4431,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884683.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884685.1",
"protein_id": "ENSP00000554744.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1083,
"cdna_end": null,
"cdna_length": 3429,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884685.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000884686.1",
"protein_id": "ENSP00000554745.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1232,
"cdna_end": null,
"cdna_length": 2841,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000884686.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000967275.1",
"protein_id": "ENSP00000637334.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1414,
"cdna_end": null,
"cdna_length": 4659,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967275.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000967276.1",
"protein_id": "ENSP00000637335.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1217,
"cdna_end": null,
"cdna_length": 4460,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967276.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000967277.1",
"protein_id": "ENSP00000637336.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
"cds_end": null,
"cds_length": 2073,
"cdna_start": 1300,
"cdna_end": null,
"cdna_length": 4554,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967277.1"
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RASGRP3",
"gene_hgnc_id": 14545,
"hgvs_c": "c.680A>T",
"hgvs_p": "p.Asn227Ile",
"transcript": "ENST00000967279.1",
"protein_id": "ENSP00000637338.1",
"transcript_support_level": null,
"aa_start": 227,
"aa_end": null,
"aa_length": 690,
"cds_start": 680,
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"bayesdelnoaf_score": -0.29,
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"acmg_score": 2,
"acmg_classification": "Uncertain_significance",
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{
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"verdict": "Uncertain_significance",
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"inheritance_mode": "AR",
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],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}