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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: 2-165764894-AG-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=165764894&ref=AG&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 165764894,
"ref": "AG",
"alt": "A",
"effect": "frameshift_variant",
"transcript": "NM_004482.4",
"consequences": [
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "NM_004482.4",
"protein_id": "NP_004473.2",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000392701.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004482.4"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000392701.8",
"protein_id": "ENSP00000376465.3",
"transcript_support_level": 1,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_004482.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392701.8"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.737delC",
"hgvs_p": "p.Ala246fs",
"transcript": "ENST00000902717.1",
"protein_id": "ENSP00000572776.1",
"transcript_support_level": null,
"aa_start": 246,
"aa_end": null,
"aa_length": 653,
"cds_start": 737,
"cds_end": null,
"cds_length": 1962,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902717.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000715282.1",
"protein_id": "ENSP00000520447.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000715282.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000902718.1",
"protein_id": "ENSP00000572777.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902718.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000916822.1",
"protein_id": "ENSP00000586881.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916822.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000916823.1",
"protein_id": "ENSP00000586882.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916823.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000916824.1",
"protein_id": "ENSP00000586883.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000916824.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000970388.1",
"protein_id": "ENSP00000640447.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970388.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000902715.1",
"protein_id": "ENSP00000572774.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 599,
"cds_start": 677,
"cds_end": null,
"cds_length": 1800,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902715.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000902716.1",
"protein_id": "ENSP00000572775.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 566,
"cds_start": 677,
"cds_end": null,
"cds_length": 1701,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902716.1"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "ENST00000412248.5",
"protein_id": "ENSP00000412643.1",
"transcript_support_level": 5,
"aa_start": 226,
"aa_end": null,
"aa_length": 463,
"cds_start": 677,
"cds_end": null,
"cds_length": 1392,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000412248.5"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "XM_005246449.2",
"protein_id": "XP_005246506.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005246449.2"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "XM_011510929.2",
"protein_id": "XP_011509231.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011510929.2"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "XM_017003770.2",
"protein_id": "XP_016859259.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 633,
"cds_start": 677,
"cds_end": null,
"cds_length": 1902,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017003770.2"
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs",
"transcript": "XM_047443883.1",
"protein_id": "XP_047299839.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 401,
"cds_start": 677,
"cds_end": null,
"cds_length": 1206,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047443883.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"hgvs_c": "n.65delC",
"hgvs_p": null,
"transcript": "ENST00000437849.1",
"protein_id": "ENSP00000391104.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000437849.1"
}
],
"gene_symbol": "GALNT3",
"gene_hgnc_id": 4125,
"dbsnp": "rs786205250",
"frequency_reference_population": 6.8406564e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84066e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": null,
"computational_prediction_selected": null,
"computational_source_selected": null,
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 8.145,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.02,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 11,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PVS1,PM2,PP5",
"acmg_by_gene": [
{
"score": 11,
"benign_score": 0,
"pathogenic_score": 11,
"criteria": [
"PVS1",
"PM2",
"PP5"
],
"verdict": "Pathogenic",
"transcript": "NM_004482.4",
"gene_symbol": "GALNT3",
"hgnc_id": 4125,
"effects": [
"frameshift_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.677delC",
"hgvs_p": "p.Ala226fs"
}
],
"clinvar_disease": " 1, familial, hyperphosphatemic,Tumoral calcinosis",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Tumoral calcinosis, hyperphosphatemic, familial, 1",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}