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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: 17-58206328-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=58206328&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"effects": [
"missense_variant"
],
"gene_symbol": "MKS1",
"hgnc_id": 7121,
"hgvs_c": "c.1460C>G",
"hgvs_p": "p.Pro487Arg",
"inheritance_mode": "AR,Unknown",
"pathogenic_score": 2,
"score": 0,
"transcript": "NM_001321269.2",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_score": 0,
"allele_count_reference_population": 4,
"alphamissense_prediction": null,
"alphamissense_score": 0.1227,
"alt": "C",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.22,
"chr": "17",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "MKS1-related disorder",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.25522762537002563,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 559,
"aa_ref": "R",
"aa_start": 515,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2343,
"cdna_start": 1568,
"cds_end": null,
"cds_length": 1680,
"cds_start": 1543,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "NM_017777.4",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1543C>G",
"hgvs_p": "p.Arg515Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000393119.7",
"protein_coding": true,
"protein_id": "NP_060247.2",
"strand": false,
"transcript": "NM_017777.4",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 559,
"aa_ref": "R",
"aa_start": 515,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2343,
"cdna_start": 1568,
"cds_end": null,
"cds_length": 1680,
"cds_start": 1543,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000393119.7",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1543C>G",
"hgvs_p": "p.Arg515Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_017777.4",
"protein_coding": true,
"protein_id": "ENSP00000376827.2",
"strand": false,
"transcript": "ENST00000393119.7",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 416,
"aa_ref": "R",
"aa_start": 372,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2083,
"cdna_start": 1607,
"cds_end": null,
"cds_length": 1251,
"cds_start": 1114,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000537529.7",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1114C>G",
"hgvs_p": "p.Arg372Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000442096.3",
"strand": false,
"transcript": "ENST00000537529.7",
"transcript_support_level": 1
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 570,
"aa_ref": "R",
"aa_start": 526,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2350,
"cdna_start": 1582,
"cds_end": null,
"cds_length": 1713,
"cds_start": 1576,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000966002.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1576C>G",
"hgvs_p": "p.Arg526Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000636061.1",
"strand": false,
"transcript": "ENST00000966002.1",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 561,
"aa_ref": "P",
"aa_start": 487,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2260,
"cdna_start": 1485,
"cds_end": null,
"cds_length": 1686,
"cds_start": 1460,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "NM_001321269.2",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1460C>G",
"hgvs_p": "p.Pro487Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001308198.1",
"strand": false,
"transcript": "NM_001321269.2",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 561,
"aa_ref": "P",
"aa_start": 487,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2260,
"cdna_start": 1485,
"cds_end": null,
"cds_length": 1686,
"cds_start": 1460,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000678463.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1460C>G",
"hgvs_p": "p.Pro487Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000502984.1",
"strand": false,
"transcript": "ENST00000678463.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 551,
"aa_ref": "R",
"aa_start": 507,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2407,
"cdna_start": 1541,
"cds_end": null,
"cds_length": 1656,
"cds_start": 1519,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000872459.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1519C>G",
"hgvs_p": "p.Arg507Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000542518.1",
"strand": false,
"transcript": "ENST00000872459.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 540,
"aa_ref": "R",
"aa_start": 496,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2284,
"cdna_start": 1509,
"cds_end": null,
"cds_length": 1623,
"cds_start": 1486,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000872460.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1486C>G",
"hgvs_p": "p.Arg496Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000542519.1",
"strand": false,
"transcript": "ENST00000872460.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 516,
"aa_ref": "R",
"aa_start": 472,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2214,
"cdna_start": 1439,
"cds_end": null,
"cds_length": 1551,
"cds_start": 1414,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000676787.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1414C>G",
"hgvs_p": "p.Arg472Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000503999.1",
"strand": false,
"transcript": "ENST00000676787.1",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 356,
"aa_ref": "R",
"aa_start": 312,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2245,
"cdna_start": 1470,
"cds_end": null,
"cds_length": 1071,
"cds_start": 934,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "NM_001321268.2",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.934C>G",
"hgvs_p": "p.Arg312Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001308197.1",
"strand": false,
"transcript": "NM_001321268.2",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 564,
"aa_ref": "P",
"aa_start": 490,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2269,
"cdna_start": 1494,
"cds_end": null,
"cds_length": 1695,
"cds_start": 1469,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "XM_011524957.3",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1469C>G",
"hgvs_p": "p.Pro490Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011523259.1",
"strand": false,
"transcript": "XM_011524957.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 562,
"aa_ref": "R",
"aa_start": 518,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2352,
"cdna_start": 1577,
"cds_end": null,
"cds_length": 1689,
"cds_start": 1552,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "XM_011524958.3",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1552C>G",
"hgvs_p": "p.Arg518Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011523260.1",
"strand": false,
"transcript": "XM_011524958.3",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 418,
"aa_ref": "P",
"aa_start": 344,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1961,
"cdna_start": 1186,
"cds_end": null,
"cds_length": 1257,
"cds_start": 1031,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "XM_005257485.5",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1031C>G",
"hgvs_p": "p.Pro344Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_005257542.1",
"strand": false,
"transcript": "XM_005257485.5",
"transcript_support_level": null
},
{
"aa_alt": "R",
"aa_end": null,
"aa_length": 358,
"aa_ref": "P",
"aa_start": 284,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1797,
"cdna_start": 1022,
"cds_end": null,
"cds_length": 1077,
"cds_start": 851,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047436333.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.851C>G",
"hgvs_p": "p.Pro284Arg",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047292289.1",
"strand": false,
"transcript": "XM_047436333.1",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 456,
"aa_ref": "T",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2126,
"cdna_start": 1351,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1326,
"consequences": [
"synonymous_variant"
],
"exon_count": 16,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "NM_001330397.2",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1326C>G",
"hgvs_p": "p.Thr442Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001317326.1",
"strand": false,
"transcript": "NM_001330397.2",
"transcript_support_level": null
},
{
"aa_alt": "T",
"aa_end": null,
"aa_length": 456,
"aa_ref": "T",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2126,
"cdna_start": 1351,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1326,
"consequences": [
"synonymous_variant"
],
"exon_count": 16,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000313863.11",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "c.1326C>G",
"hgvs_p": "p.Thr442Thr",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000316631.6",
"strand": false,
"transcript": "ENST00000313863.11",
"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": 1926,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000393120.6",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "n.*950C>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000376828.2",
"strand": false,
"transcript": "ENST00000393120.6",
"transcript_support_level": 2
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 697,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 3,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000583577.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "n.369C>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000583577.1",
"transcript_support_level": 2
},
{
"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": 2403,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 18,
"exon_rank": 17,
"exon_rank_end": null,
"feature": "ENST00000675753.2",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "n.*1162C>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000502156.1",
"strand": false,
"transcript": "ENST00000675753.2",
"transcript_support_level": null
},
{
"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": 2771,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 15,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000677111.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "n.*1017C>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000504282.1",
"strand": false,
"transcript": "ENST00000677111.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 3592,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 17,
"exon_rank": 16,
"exon_rank_end": null,
"feature": "ENST00000677160.1",
"gene_hgnc_id": 7121,
"gene_symbol": "MKS1",
"hgvs_c": "n.2817C>G",
"hgvs_p": null,
"intron_rank": null,
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