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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: 12-47978015-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=47978015&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 47978015,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001844.5",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3106C>G",
"hgvs_p": "p.Arg1036Gly",
"transcript": "NM_001844.5",
"protein_id": "NP_001835.3",
"transcript_support_level": null,
"aa_start": 1036,
"aa_end": null,
"aa_length": 1487,
"cds_start": 3106,
"cds_end": null,
"cds_length": 4464,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000380518.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001844.5"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3106C>G",
"hgvs_p": "p.Arg1036Gly",
"transcript": "ENST00000380518.8",
"protein_id": "ENSP00000369889.3",
"transcript_support_level": 1,
"aa_start": 1036,
"aa_end": null,
"aa_length": 1487,
"cds_start": 3106,
"cds_end": null,
"cds_length": 4464,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001844.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380518.8"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.2899C>G",
"hgvs_p": "p.Arg967Gly",
"transcript": "ENST00000337299.7",
"protein_id": "ENSP00000338213.6",
"transcript_support_level": 1,
"aa_start": 967,
"aa_end": null,
"aa_length": 1418,
"cds_start": 2899,
"cds_end": null,
"cds_length": 4257,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000337299.7"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3109C>G",
"hgvs_p": "p.Arg1037Gly",
"transcript": "ENST00000928357.1",
"protein_id": "ENSP00000598416.1",
"transcript_support_level": null,
"aa_start": 1037,
"aa_end": null,
"aa_length": 1488,
"cds_start": 3109,
"cds_end": null,
"cds_length": 4467,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928357.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.2899C>G",
"hgvs_p": "p.Arg967Gly",
"transcript": "NM_033150.3",
"protein_id": "NP_149162.2",
"transcript_support_level": null,
"aa_start": 967,
"aa_end": null,
"aa_length": 1418,
"cds_start": 2899,
"cds_end": null,
"cds_length": 4257,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_033150.3"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 46,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3250C>G",
"hgvs_p": "p.Arg1084Gly",
"transcript": "XM_017018828.1",
"protein_id": "XP_016874317.1",
"transcript_support_level": null,
"aa_start": 1084,
"aa_end": null,
"aa_length": 1535,
"cds_start": 3250,
"cds_end": null,
"cds_length": 4608,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017018828.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 46,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3247C>G",
"hgvs_p": "p.Arg1083Gly",
"transcript": "XM_017018829.1",
"protein_id": "XP_016874318.1",
"transcript_support_level": null,
"aa_start": 1083,
"aa_end": null,
"aa_length": 1534,
"cds_start": 3247,
"cds_end": null,
"cds_length": 4605,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017018829.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 45,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.3040C>G",
"hgvs_p": "p.Arg1014Gly",
"transcript": "XM_017018830.1",
"protein_id": "XP_016874319.1",
"transcript_support_level": null,
"aa_start": 1014,
"aa_end": null,
"aa_length": 1465,
"cds_start": 3040,
"cds_end": null,
"cds_length": 4398,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017018830.1"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.2560C>G",
"hgvs_p": "p.Arg854Gly",
"transcript": "XM_017018831.3",
"protein_id": "XP_016874320.1",
"transcript_support_level": null,
"aa_start": 854,
"aa_end": null,
"aa_length": 1305,
"cds_start": 2560,
"cds_end": null,
"cds_length": 3918,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017018831.3"
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 44,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "c.2560C>G",
"hgvs_p": "p.Arg854Gly",
"transcript": "XM_047428315.1",
"protein_id": "XP_047284271.1",
"transcript_support_level": null,
"aa_start": 854,
"aa_end": null,
"aa_length": 1305,
"cds_start": 2560,
"cds_end": null,
"cds_length": 3918,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047428315.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"hgvs_c": "n.2192C>G",
"hgvs_p": null,
"transcript": "ENST00000493991.5",
"protein_id": null,
"transcript_support_level": 2,
"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": "pseudogene",
"feature": "ENST00000493991.5"
}
],
"gene_symbol": "COL2A1",
"gene_hgnc_id": 2200,
"dbsnp": "rs748459670",
"frequency_reference_population": 0.000027275726,
"hom_count_reference_population": 3,
"allele_count_reference_population": 44,
"gnomad_exomes_af": 0.0000294304,
"gnomad_genomes_af": 0.00000657549,
"gnomad_exomes_ac": 43,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 3,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9036324620246887,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.79,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.5838,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.33,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 2.623,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.05,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM1,PP2,PP3_Moderate,BP6,BS2",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 5,
"pathogenic_score": 5,
"criteria": [
"PM1",
"PP2",
"PP3_Moderate",
"BP6",
"BS2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001844.5",
"gene_symbol": "COL2A1",
"hgnc_id": 2200,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR,Unknown",
"hgvs_c": "c.3106C>G",
"hgvs_p": "p.Arg1036Gly"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:2 LB:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}