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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: 2-127423407-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=127423407&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 5,
"criteria": [
"BP4_Strong",
"BP7"
],
"effects": [
"splice_region_variant",
"synonymous_variant"
],
"gene_symbol": "PROC",
"hgnc_id": 9451,
"hgvs_c": "c.720A>G",
"hgvs_p": "p.Ala240Ala",
"inheritance_mode": "SD,AD,AR",
"pathogenic_score": 0,
"score": -5,
"transcript": "NM_001375607.1",
"verdict": "Likely_benign"
},
{
"benign_score": 4,
"criteria": [
"BP4_Strong"
],
"effects": [
"downstream_gene_variant"
],
"gene_symbol": "MIR4783",
"hgnc_id": 41874,
"hgvs_c": "n.*130T>C",
"hgvs_p": null,
"inheritance_mode": "",
"pathogenic_score": 0,
"score": -4,
"transcript": "NR_039944.1",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong,BP7",
"acmg_score": -5,
"allele_count_reference_population": 182,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.77,
"chr": "2",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": " autosomal dominant, autosomal recessive,Thrombophilia due to protein C deficiency",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.009999999776482582,
"computational_source_selected": "REVEL",
"consequences": [
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 461,
"aa_ref": "A",
"aa_start": 178,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1769,
"cdna_start": 621,
"cds_end": null,
"cds_length": 1386,
"cds_start": 534,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NM_000312.4",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.534A>G",
"hgvs_p": "p.Ala178Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000234071.8",
"protein_coding": true,
"protein_id": "NP_000303.1",
"strand": true,
"transcript": "NM_000312.4",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 461,
"aa_ref": "A",
"aa_start": 178,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1769,
"cdna_start": 621,
"cds_end": null,
"cds_length": 1386,
"cds_start": 534,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000234071.8",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.534A>G",
"hgvs_p": "p.Ala178Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000312.4",
"protein_coding": true,
"protein_id": "ENSP00000234071.4",
"strand": true,
"transcript": "ENST00000234071.8",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 272,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1734,
"cdna_start": null,
"cds_end": null,
"cds_length": 819,
"cds_start": null,
"consequences": [
"splice_region_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "XM_017004505.2",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.-34A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016859994.2",
"strand": true,
"transcript": "XM_017004505.2",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 523,
"aa_ref": "A",
"aa_start": 240,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1888,
"cdna_start": 740,
"cds_end": null,
"cds_length": 1572,
"cds_start": 720,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_001375607.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.720A>G",
"hgvs_p": "p.Ala240Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001362536.1",
"strand": true,
"transcript": "NM_001375607.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 522,
"aa_ref": "A",
"aa_start": 239,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1885,
"cdna_start": 737,
"cds_end": null,
"cds_length": 1569,
"cds_start": 717,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 9,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "NM_001375602.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.717A>G",
"hgvs_p": "p.Ala239Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001362531.1",
"strand": true,
"transcript": "NM_001375602.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 519,
"aa_ref": "A",
"aa_start": 236,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1721,
"cdna_start": 802,
"cds_end": null,
"cds_length": 1560,
"cds_start": 708,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883860.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.708A>G",
"hgvs_p": "p.Ala236Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553919.1",
"strand": true,
"transcript": "ENST00000883860.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 519,
"aa_ref": "A",
"aa_start": 236,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2118,
"cdna_start": 997,
"cds_end": null,
"cds_length": 1560,
"cds_start": 708,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000883897.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.708A>G",
"hgvs_p": "p.Ala236Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553956.1",
"strand": true,
"transcript": "ENST00000883897.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 517,
"aa_ref": "A",
"aa_start": 234,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1870,
"cdna_start": 722,
"cds_end": null,
"cds_length": 1554,
"cds_start": 702,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_001375606.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.702A>G",
"hgvs_p": "p.Ala234Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001362535.1",
"strand": true,
"transcript": "NM_001375606.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 516,
"aa_ref": "A",
"aa_start": 233,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1867,
"cdna_start": 719,
"cds_end": null,
"cds_length": 1551,
"cds_start": 699,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_001375603.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.699A>G",
"hgvs_p": "p.Ala233Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001362532.1",
"strand": true,
"transcript": "NM_001375603.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 512,
"aa_ref": "A",
"aa_start": 229,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1853,
"cdna_start": 933,
"cds_end": null,
"cds_length": 1539,
"cds_start": 687,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000883902.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.687A>G",
"hgvs_p": "p.Ala229Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553961.1",
"strand": true,
"transcript": "ENST00000883902.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1871,
"cdna_start": 723,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "NM_001375605.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001362534.1",
"strand": true,
"transcript": "NM_001375605.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1586,
"cdna_start": 697,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000409048.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000386679.1",
"strand": true,
"transcript": "ENST00000409048.1",
"transcript_support_level": 5
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1984,
"cdna_start": 830,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883843.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553902.1",
"strand": true,
"transcript": "ENST00000883843.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1980,
"cdna_start": 826,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883844.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553903.1",
"strand": true,
"transcript": "ENST00000883844.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1855,
"cdna_start": 734,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883854.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553913.1",
"strand": true,
"transcript": "ENST00000883854.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2151,
"cdna_start": 1000,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883858.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553917.1",
"strand": true,
"transcript": "ENST00000883858.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1661,
"cdna_start": 742,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883861.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553920.1",
"strand": true,
"transcript": "ENST00000883861.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1865,
"cdna_start": 945,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883880.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553939.1",
"strand": true,
"transcript": "ENST00000883880.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1984,
"cdna_start": 833,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883881.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553940.1",
"strand": true,
"transcript": "ENST00000883881.1",
"transcript_support_level": null
},
{
"aa_alt": "A",
"aa_end": null,
"aa_length": 495,
"aa_ref": "A",
"aa_start": 212,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1943,
"cdna_start": 822,
"cds_end": null,
"cds_length": 1488,
"cds_start": 636,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000883888.1",
"gene_hgnc_id": 9451,
"gene_symbol": "PROC",
"hgvs_c": "c.636A>G",
"hgvs_p": "p.Ala212Ala",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000553947.1",
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