← Back to variant description
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: 2-218264538-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=218264538&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 218264538,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001302545.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1300C>A",
"hgvs_p": "p.Arg434Ser",
"transcript": "NM_001087.5",
"protein_id": "NP_001078.2",
"transcript_support_level": null,
"aa_start": 434,
"aa_end": null,
"aa_length": 434,
"cds_start": 1300,
"cds_end": null,
"cds_length": 1305,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000248450.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001087.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1300C>A",
"hgvs_p": "p.Arg434Ser",
"transcript": "ENST00000248450.9",
"protein_id": "ENSP00000248450.4",
"transcript_support_level": 1,
"aa_start": 434,
"aa_end": null,
"aa_length": 434,
"cds_start": 1300,
"cds_end": null,
"cds_length": 1305,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001087.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000248450.9"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1303C>A",
"hgvs_p": "p.Arg435Ser",
"transcript": "ENST00000444053.5",
"protein_id": "ENSP00000403343.1",
"transcript_support_level": 1,
"aa_start": 435,
"aa_end": null,
"aa_length": 435,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1308,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000444053.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1303C>A",
"hgvs_p": "p.Arg435Ser",
"transcript": "NM_001302545.2",
"protein_id": "NP_001289474.1",
"transcript_support_level": null,
"aa_start": 435,
"aa_end": null,
"aa_length": 435,
"cds_start": 1303,
"cds_end": null,
"cds_length": 1308,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001302545.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1291C>A",
"hgvs_p": "p.Arg431Ser",
"transcript": "ENST00000896972.1",
"protein_id": "ENSP00000567031.1",
"transcript_support_level": null,
"aa_start": 431,
"aa_end": null,
"aa_length": 431,
"cds_start": 1291,
"cds_end": null,
"cds_length": 1296,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896972.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1285C>A",
"hgvs_p": "p.Arg429Ser",
"transcript": "ENST00000912377.1",
"protein_id": "ENSP00000582436.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 429,
"cds_start": 1285,
"cds_end": null,
"cds_length": 1290,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912377.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1282C>A",
"hgvs_p": "p.Arg428Ser",
"transcript": "ENST00000952048.1",
"protein_id": "ENSP00000622107.1",
"transcript_support_level": null,
"aa_start": 428,
"aa_end": null,
"aa_length": 428,
"cds_start": 1282,
"cds_end": null,
"cds_length": 1287,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952048.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1261C>A",
"hgvs_p": "p.Arg421Ser",
"transcript": "ENST00000952045.1",
"protein_id": "ENSP00000622104.1",
"transcript_support_level": null,
"aa_start": 421,
"aa_end": null,
"aa_length": 421,
"cds_start": 1261,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952045.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1255C>A",
"hgvs_p": "p.Arg419Ser",
"transcript": "ENST00000952043.1",
"protein_id": "ENSP00000622102.1",
"transcript_support_level": null,
"aa_start": 419,
"aa_end": null,
"aa_length": 419,
"cds_start": 1255,
"cds_end": null,
"cds_length": 1260,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952043.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1252C>A",
"hgvs_p": "p.Arg418Ser",
"transcript": "ENST00000952044.1",
"protein_id": "ENSP00000622103.1",
"transcript_support_level": null,
"aa_start": 418,
"aa_end": null,
"aa_length": 418,
"cds_start": 1252,
"cds_end": null,
"cds_length": 1257,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952044.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1243C>A",
"hgvs_p": "p.Arg415Ser",
"transcript": "ENST00000420660.5",
"protein_id": "ENSP00000416394.1",
"transcript_support_level": 2,
"aa_start": 415,
"aa_end": null,
"aa_length": 415,
"cds_start": 1243,
"cds_end": null,
"cds_length": 1248,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000420660.5"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1219C>A",
"hgvs_p": "p.Arg407Ser",
"transcript": "ENST00000952047.1",
"protein_id": "ENSP00000622106.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 407,
"cds_start": 1219,
"cds_end": null,
"cds_length": 1224,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952047.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1216C>A",
"hgvs_p": "p.Arg406Ser",
"transcript": "ENST00000896971.1",
"protein_id": "ENSP00000567030.1",
"transcript_support_level": null,
"aa_start": 406,
"aa_end": null,
"aa_length": 406,
"cds_start": 1216,
"cds_end": null,
"cds_length": 1221,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896971.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1180C>A",
"hgvs_p": "p.Arg394Ser",
"transcript": "ENST00000896973.1",
"protein_id": "ENSP00000567032.1",
"transcript_support_level": null,
"aa_start": 394,
"aa_end": null,
"aa_length": 394,
"cds_start": 1180,
"cds_end": null,
"cds_length": 1185,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896973.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1147C>A",
"hgvs_p": "p.Arg383Ser",
"transcript": "ENST00000952046.1",
"protein_id": "ENSP00000622105.1",
"transcript_support_level": null,
"aa_start": 383,
"aa_end": null,
"aa_length": 383,
"cds_start": 1147,
"cds_end": null,
"cds_length": 1152,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000952046.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.1105C>A",
"hgvs_p": "p.Arg369Ser",
"transcript": "ENST00000912378.1",
"protein_id": "ENSP00000582437.1",
"transcript_support_level": null,
"aa_start": 369,
"aa_end": null,
"aa_length": 369,
"cds_start": 1105,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912378.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "c.562C>A",
"hgvs_p": "p.Arg188Ser",
"transcript": "ENST00000422731.1",
"protein_id": "ENSP00000396295.1",
"transcript_support_level": 3,
"aa_start": 188,
"aa_end": null,
"aa_length": 188,
"cds_start": 562,
"cds_end": null,
"cds_length": 567,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000422731.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "n.1862C>A",
"hgvs_p": null,
"transcript": "ENST00000475678.5",
"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": "retained_intron",
"feature": "ENST00000475678.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "n.1478C>A",
"hgvs_p": null,
"transcript": "ENST00000489767.5",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000489767.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"hgvs_c": "n.777C>A",
"hgvs_p": null,
"transcript": "ENST00000494720.5",
"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": "retained_intron",
"feature": "ENST00000494720.5"
}
],
"gene_symbol": "AAMP",
"gene_hgnc_id": 18,
"dbsnp": "rs773199979",
"frequency_reference_population": 6.8411805e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84118e-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": 0.6521857976913452,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.236,
"revel_prediction": "Benign",
"alphamissense_score": 0.9521,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 9.678,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001302545.2",
"gene_symbol": "AAMP",
"hgnc_id": 18,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1303C>A",
"hgvs_p": "p.Arg435Ser"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}