← 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: 14-23128047-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=23128047&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 23128047,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_012244.4",
"consequences": [
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.1413C>G",
"hgvs_p": "p.His471Gln",
"transcript": "NM_012244.4",
"protein_id": "NP_036376.2",
"transcript_support_level": null,
"aa_start": 471,
"aa_end": null,
"aa_length": 535,
"cds_start": 1413,
"cds_end": null,
"cds_length": 1608,
"cdna_start": 2159,
"cdna_end": null,
"cdna_length": 4236,
"mane_select": "ENST00000316902.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012244.4"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.1413C>G",
"hgvs_p": "p.His471Gln",
"transcript": "ENST00000316902.12",
"protein_id": "ENSP00000320378.7",
"transcript_support_level": 1,
"aa_start": 471,
"aa_end": null,
"aa_length": 535,
"cds_start": 1413,
"cds_end": null,
"cds_length": 1608,
"cdna_start": 2159,
"cdna_end": null,
"cdna_length": 4236,
"mane_select": "NM_012244.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000316902.12"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.804C>G",
"hgvs_p": "p.His268Gln",
"transcript": "ENST00000453702.5",
"protein_id": "ENSP00000391577.1",
"transcript_support_level": 1,
"aa_start": 268,
"aa_end": null,
"aa_length": 332,
"cds_start": 804,
"cds_end": null,
"cds_length": 999,
"cdna_start": 1048,
"cdna_end": null,
"cdna_length": 1752,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000453702.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.789-704C>G",
"hgvs_p": null,
"transcript": "ENST00000469263.5",
"protein_id": "ENSP00000435114.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 289,
"cds_start": null,
"cds_end": null,
"cds_length": 870,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3557,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000469263.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.*297C>G",
"hgvs_p": null,
"transcript": "ENST00000339733.9",
"protein_id": "ENSP00000343949.5",
"transcript_support_level": 1,
"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": 3066,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000339733.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.*297C>G",
"hgvs_p": null,
"transcript": "ENST00000339733.9",
"protein_id": "ENSP00000343949.5",
"transcript_support_level": 1,
"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": 3066,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000339733.9"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.1098C>G",
"hgvs_p": "p.His366Gln",
"transcript": "NM_001267036.1",
"protein_id": "NP_001253965.1",
"transcript_support_level": null,
"aa_start": 366,
"aa_end": null,
"aa_length": 430,
"cds_start": 1098,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 1198,
"cdna_end": null,
"cdna_length": 3275,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001267036.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.1098C>G",
"hgvs_p": "p.His366Gln",
"transcript": "ENST00000529705.6",
"protein_id": "ENSP00000434345.2",
"transcript_support_level": 2,
"aa_start": 366,
"aa_end": null,
"aa_length": 430,
"cds_start": 1098,
"cds_end": null,
"cds_length": 1293,
"cdna_start": 1198,
"cdna_end": null,
"cdna_length": 1819,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000529705.6"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.804C>G",
"hgvs_p": "p.His268Gln",
"transcript": "NM_182728.3",
"protein_id": "NP_877392.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 332,
"cds_start": 804,
"cds_end": null,
"cds_length": 999,
"cdna_start": 1040,
"cdna_end": null,
"cdna_length": 3117,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_182728.3"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.741C>G",
"hgvs_p": "p.His247Gln",
"transcript": "NM_001267037.2",
"protein_id": "NP_001253966.1",
"transcript_support_level": null,
"aa_start": 247,
"aa_end": null,
"aa_length": 311,
"cds_start": 741,
"cds_end": null,
"cds_length": 936,
"cdna_start": 886,
"cdna_end": null,
"cdna_length": 2963,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001267037.2"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "c.741C>G",
"hgvs_p": "p.His247Gln",
"transcript": "ENST00000422941.6",
"protein_id": "ENSP00000416398.2",
"transcript_support_level": 2,
"aa_start": 247,
"aa_end": null,
"aa_length": 311,
"cds_start": 741,
"cds_end": null,
"cds_length": 936,
"cdna_start": 943,
"cdna_end": null,
"cdna_length": 3018,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000422941.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.644C>G",
"hgvs_p": null,
"transcript": "ENST00000397310.6",
"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": 2719,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000397310.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.*500C>G",
"hgvs_p": null,
"transcript": "ENST00000528860.5",
"protein_id": "ENSP00000435865.1",
"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": 1499,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000528860.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.1000C>G",
"hgvs_p": null,
"transcript": "NR_049767.2",
"protein_id": null,
"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": 3077,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_049767.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"hgvs_c": "n.*500C>G",
"hgvs_p": null,
"transcript": "ENST00000528860.5",
"protein_id": "ENSP00000435865.1",
"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": 1499,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000528860.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000295888",
"gene_hgnc_id": null,
"hgvs_c": "n.235-8942G>C",
"hgvs_p": null,
"transcript": "ENST00000733532.1",
"protein_id": null,
"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": 540,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000733532.1"
}
],
"gene_symbol": "SLC7A8",
"gene_hgnc_id": 11066,
"dbsnp": "rs2048595204",
"frequency_reference_population": 0.0000013681332,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000136813,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.1622263491153717,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.194,
"revel_prediction": "Benign",
"alphamissense_score": 0.0817,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.23,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.92,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_012244.4",
"gene_symbol": "SLC7A8",
"hgnc_id": 11066,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1413C>G",
"hgvs_p": "p.His471Gln"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000733532.1",
"gene_symbol": "ENSG00000295888",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.235-8942G>C",
"hgvs_p": null
}
],
"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
}