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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: 9-38577917-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=38577917&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 38577917,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001331100.2",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2479G>A",
"hgvs_p": "p.Asp827Asn",
"transcript": "NM_147195.4",
"protein_id": "NP_671728.2",
"transcript_support_level": null,
"aa_start": 827,
"aa_end": null,
"aa_length": 992,
"cds_start": 2479,
"cds_end": null,
"cds_length": 2979,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000399703.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_147195.4"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2479G>A",
"hgvs_p": "p.Asp827Asn",
"transcript": "ENST00000399703.6",
"protein_id": "ENSP00000382610.4",
"transcript_support_level": 1,
"aa_start": 827,
"aa_end": null,
"aa_length": 992,
"cds_start": 2479,
"cds_end": null,
"cds_length": 2979,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_147195.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000399703.6"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.649G>A",
"hgvs_p": "p.Asp217Asn",
"transcript": "ENST00000602295.5",
"protein_id": "ENSP00000473463.1",
"transcript_support_level": 1,
"aa_start": 217,
"aa_end": null,
"aa_length": 401,
"cds_start": 649,
"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": "ENST00000602295.5"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2665G>A",
"hgvs_p": "p.Asp889Asn",
"transcript": "NM_001331100.2",
"protein_id": "NP_001318029.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 1054,
"cds_start": 2665,
"cds_end": null,
"cds_length": 3165,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001331100.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2665G>A",
"hgvs_p": "p.Asp889Asn",
"transcript": "ENST00000703205.1",
"protein_id": "ENSP00000515234.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 1054,
"cds_start": 2665,
"cds_end": null,
"cds_length": 3165,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000703205.1"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2479G>A",
"hgvs_p": "p.Asp827Asn",
"transcript": "XM_024447483.2",
"protein_id": "XP_024303251.1",
"transcript_support_level": null,
"aa_start": 827,
"aa_end": null,
"aa_length": 1170,
"cds_start": 2479,
"cds_end": null,
"cds_length": 3513,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447483.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2668G>A",
"hgvs_p": "p.Asp890Asn",
"transcript": "XM_024447479.2",
"protein_id": "XP_024303247.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 1127,
"cds_start": 2668,
"cds_end": null,
"cds_length": 3384,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447479.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2668G>A",
"hgvs_p": "p.Asp890Asn",
"transcript": "XM_024447480.2",
"protein_id": "XP_024303248.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 1126,
"cds_start": 2668,
"cds_end": null,
"cds_length": 3381,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447480.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2668G>A",
"hgvs_p": "p.Asp890Asn",
"transcript": "XM_024447481.2",
"protein_id": "XP_024303249.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 1119,
"cds_start": 2668,
"cds_end": null,
"cds_length": 3360,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447481.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2668G>A",
"hgvs_p": "p.Asp890Asn",
"transcript": "XM_024447482.2",
"protein_id": "XP_024303250.1",
"transcript_support_level": null,
"aa_start": 890,
"aa_end": null,
"aa_length": 1055,
"cds_start": 2668,
"cds_end": null,
"cds_length": 3168,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024447482.2"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2665G>A",
"hgvs_p": "p.Asp889Asn",
"transcript": "XM_017014576.3",
"protein_id": "XP_016870065.1",
"transcript_support_level": null,
"aa_start": 889,
"aa_end": null,
"aa_length": 1054,
"cds_start": 2665,
"cds_end": null,
"cds_length": 3165,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017014576.3"
},
{
"aa_ref": "D",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "c.2479G>A",
"hgvs_p": "p.Asp827Asn",
"transcript": "XM_011517839.4",
"protein_id": "XP_011516141.1",
"transcript_support_level": null,
"aa_start": 827,
"aa_end": null,
"aa_length": 992,
"cds_start": 2479,
"cds_end": null,
"cds_length": 2979,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011517839.4"
},
{
"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": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "n.*1439G>A",
"hgvs_p": null,
"transcript": "ENST00000703204.1",
"protein_id": "ENSP00000515233.1",
"transcript_support_level": null,
"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": "ENST00000703204.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"hgvs_c": "n.*1439G>A",
"hgvs_p": null,
"transcript": "ENST00000703204.1",
"protein_id": "ENSP00000515233.1",
"transcript_support_level": null,
"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": "ENST00000703204.1"
}
],
"gene_symbol": "ANKRD18A",
"gene_hgnc_id": 23643,
"dbsnp": "rs748836421",
"frequency_reference_population": 0.00011202721,
"hom_count_reference_population": 0,
"allele_count_reference_population": 179,
"gnomad_exomes_af": 0.000107911,
"gnomad_genomes_af": 0.000151133,
"gnomad_exomes_ac": 156,
"gnomad_genomes_ac": 23,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.01719146966934204,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.117,
"revel_prediction": "Benign",
"alphamissense_score": 0.1121,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.66,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.511,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_001331100.2",
"gene_symbol": "ANKRD18A",
"hgnc_id": 23643,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2665G>A",
"hgvs_p": "p.Asp889Asn"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}