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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: 3-123707882-CCA-ACG (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=123707882&ref=CCA&alt=ACG&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PP3"
],
"effects": [
"missense_variant"
],
"gene_symbol": "MYLK",
"hgnc_id": 7590,
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"inheritance_mode": "AD,Unknown,AR",
"pathogenic_score": 1,
"score": 1,
"transcript": "NM_053025.4",
"verdict": "Uncertain_significance"
},
{
"benign_score": 0,
"criteria": [
"PP3"
],
"effects": [
"intron_variant"
],
"gene_symbol": "MYLK-AS1",
"hgnc_id": 42440,
"hgvs_c": "n.611+3873_611+3875delCCAinsACG",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 1,
"score": 1,
"transcript": "ENST00000685586.1",
"verdict": "Uncertain_significance"
},
{
"benign_score": 0,
"criteria": [
"PP3"
],
"effects": [
"intron_variant"
],
"gene_symbol": "LOC105369194",
"hgnc_id": null,
"hgvs_c": "n.251+3873_251+3875delCCAinsACG",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 1,
"score": 1,
"transcript": "XR_924417.4",
"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": "ACG",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "3",
"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": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10113,
"cdna_start": 2574,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 34,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_053025.4",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000360304.8",
"protein_coding": true,
"protein_id": "NP_444253.3",
"strand": false,
"transcript": "NM_053025.4",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 10113,
"cdna_start": 2574,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 34,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000360304.8",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_053025.4",
"protein_coding": true,
"protein_id": "ENSP00000353452.3",
"strand": false,
"transcript": "ENST00000360304.8",
"transcript_support_level": 5
},
{
"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": 5901,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 33,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000464489.5",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "n.*1839_*1841delTGGinsCGT",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000417798.1",
"strand": false,
"transcript": "ENST00000464489.5",
"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": 5901,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 33,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000464489.5",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "n.*1839_*1841delTGGinsCGT",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000417798.1",
"strand": false,
"transcript": "ENST00000464489.5",
"transcript_support_level": 1
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1924,
"aa_ref": "W",
"aa_start": 764,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5956,
"cdna_start": 2454,
"cds_end": null,
"cds_length": 5775,
"cds_start": 2290,
"consequences": [
"missense_variant"
],
"exon_count": 32,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000687848.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2290_2292delTGGinsCGT",
"hgvs_p": "p.Trp764Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508761.1",
"strand": false,
"transcript": "ENST00000687848.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6162,
"cdna_start": 2621,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 32,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000686761.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508758.1",
"strand": false,
"transcript": "ENST00000686761.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6117,
"cdna_start": 2558,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000971487.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000641546.1",
"strand": false,
"transcript": "ENST00000971487.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6041,
"cdna_start": 2482,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000971488.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000641547.1",
"strand": false,
"transcript": "ENST00000971488.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8025,
"cdna_start": 2733,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 32,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000971489.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000641548.1",
"strand": false,
"transcript": "ENST00000971489.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1914,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6005,
"cdna_start": 2463,
"cds_end": null,
"cds_length": 5745,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 32,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000971490.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000641549.1",
"strand": false,
"transcript": "ENST00000971490.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1913,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5783,
"cdna_start": 2265,
"cds_end": null,
"cds_length": 5742,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 31,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000686406.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000509044.1",
"strand": false,
"transcript": "ENST00000686406.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1863,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9960,
"cdna_start": 2574,
"cds_end": null,
"cds_length": 5592,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_053027.4",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_444255.3",
"strand": false,
"transcript": "NM_053027.4",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1863,
"aa_ref": "W",
"aa_start": 754,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10027,
"cdna_start": 2641,
"cds_end": null,
"cds_length": 5592,
"cds_start": 2260,
"consequences": [
"missense_variant"
],
"exon_count": 34,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000360772.7",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2260_2262delTGGinsCGT",
"hgvs_p": "p.Trp754Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000354004.3",
"strand": false,
"transcript": "ENST00000360772.7",
"transcript_support_level": 5
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1845,
"aa_ref": "W",
"aa_start": 685,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9906,
"cdna_start": 2367,
"cds_end": null,
"cds_length": 5538,
"cds_start": 2053,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_053026.4",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2053_2055delTGGinsCGT",
"hgvs_p": "p.Trp685Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_444254.3",
"strand": false,
"transcript": "NM_053026.4",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1845,
"aa_ref": "W",
"aa_start": 685,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7398,
"cdna_start": 2349,
"cds_end": null,
"cds_length": 5538,
"cds_start": 2053,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000693689.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2053_2055delTGGinsCGT",
"hgvs_p": "p.Trp685Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000510503.1",
"strand": false,
"transcript": "ENST00000693689.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1794,
"aa_ref": "W",
"aa_start": 685,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9753,
"cdna_start": 2367,
"cds_end": null,
"cds_length": 5385,
"cds_start": 2053,
"consequences": [
"missense_variant"
],
"exon_count": 32,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_053028.4",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2053_2055delTGGinsCGT",
"hgvs_p": "p.Trp685Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_444256.3",
"strand": false,
"transcript": "NM_053028.4",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1794,
"aa_ref": "W",
"aa_start": 685,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5566,
"cdna_start": 2174,
"cds_end": null,
"cds_length": 5385,
"cds_start": 2053,
"consequences": [
"missense_variant"
],
"exon_count": 30,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000346322.10",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.2053_2055delTGGinsCGT",
"hgvs_p": "p.Trp685Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000320622.6",
"strand": false,
"transcript": "ENST00000346322.10",
"transcript_support_level": 5
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1738,
"aa_ref": "W",
"aa_start": 578,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9905,
"cdna_start": 2366,
"cds_end": null,
"cds_length": 5217,
"cds_start": 1732,
"consequences": [
"missense_variant"
],
"exon_count": 33,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001321309.2",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.1732_1734delTGGinsCGT",
"hgvs_p": "p.Trp578Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001308238.1",
"strand": false,
"transcript": "NM_001321309.2",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1660,
"aa_ref": "W",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5130,
"cdna_start": 1597,
"cds_end": null,
"cds_length": 4983,
"cds_start": 1498,
"consequences": [
"missense_variant"
],
"exon_count": 29,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000690457.1",
"gene_hgnc_id": 7590,
"gene_symbol": "MYLK",
"hgvs_c": "c.1498_1500delTGGinsCGT",
"hgvs_p": "p.Trp500Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000508777.1",
"strand": false,
"transcript": "ENST00000690457.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 1924,
"aa_ref": "W",
"aa_start": 764,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10114,
"cdna_start": 2575,
"cds_end": null,
"cds_length": 5775,
"cds_start": 2290,
"consequences": [
"missense_variant"
],
"exon_count": 34,
"exon_rank": null,
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