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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: 5-160565493-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=160565493&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 160565493,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_025153.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "NM_025153.3",
"protein_id": "NP_079429.2",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000327245.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_025153.3"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "ENST00000327245.10",
"protein_id": "ENSP00000313600.5",
"transcript_support_level": 1,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_025153.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000327245.10"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "NM_001366652.1",
"protein_id": "NP_001353581.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366652.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "NM_001366655.1",
"protein_id": "NP_001353584.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366655.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "ENST00000943128.1",
"protein_id": "ENSP00000613187.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943128.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4310G>A",
"hgvs_p": "p.Arg1437Lys",
"transcript": "NM_001366657.1",
"protein_id": "NP_001353586.1",
"transcript_support_level": null,
"aa_start": 1437,
"aa_end": null,
"aa_length": 1449,
"cds_start": 4310,
"cds_end": null,
"cds_length": 4350,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366657.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4262G>A",
"hgvs_p": "p.Arg1421Lys",
"transcript": "NM_001410822.1",
"protein_id": "NP_001397751.1",
"transcript_support_level": null,
"aa_start": 1421,
"aa_end": null,
"aa_length": 1433,
"cds_start": 4262,
"cds_end": null,
"cds_length": 4302,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001410822.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4262G>A",
"hgvs_p": "p.Arg1421Lys",
"transcript": "ENST00000642502.1",
"protein_id": "ENSP00000493802.1",
"transcript_support_level": null,
"aa_start": 1421,
"aa_end": null,
"aa_length": 1433,
"cds_start": 4262,
"cds_end": null,
"cds_length": 4302,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000642502.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "XM_011534468.3",
"protein_id": "XP_011532770.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011534468.3"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "XM_011534469.2",
"protein_id": "XP_011532771.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011534469.2"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys",
"transcript": "XM_047416994.1",
"protein_id": "XP_047272950.1",
"transcript_support_level": null,
"aa_start": 1449,
"aa_end": null,
"aa_length": 1461,
"cds_start": 4346,
"cds_end": null,
"cds_length": 4386,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416994.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4310G>A",
"hgvs_p": "p.Arg1437Lys",
"transcript": "XM_017009252.2",
"protein_id": "XP_016864741.1",
"transcript_support_level": null,
"aa_start": 1437,
"aa_end": null,
"aa_length": 1449,
"cds_start": 4310,
"cds_end": null,
"cds_length": 4350,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017009252.2"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4145G>A",
"hgvs_p": "p.Arg1382Lys",
"transcript": "XM_047416995.1",
"protein_id": "XP_047272951.1",
"transcript_support_level": null,
"aa_start": 1382,
"aa_end": null,
"aa_length": 1394,
"cds_start": 4145,
"cds_end": null,
"cds_length": 4185,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416995.1"
},
{
"aa_ref": "R",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"hgvs_c": "c.4061G>A",
"hgvs_p": "p.Arg1354Lys",
"transcript": "XM_047416996.1",
"protein_id": "XP_047272952.1",
"transcript_support_level": null,
"aa_start": 1354,
"aa_end": null,
"aa_length": 1366,
"cds_start": 4061,
"cds_end": null,
"cds_length": 4101,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416996.1"
},
{
"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": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MIR3142HG",
"gene_hgnc_id": 51944,
"hgvs_c": "n.658-35216C>T",
"hgvs_p": null,
"transcript": "ENST00000770454.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000770454.1"
},
{
"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": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MIR3142HG",
"gene_hgnc_id": 51944,
"hgvs_c": "n.563-35216C>T",
"hgvs_p": null,
"transcript": "ENST00000770455.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000770455.1"
},
{
"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": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MIR3142HG",
"gene_hgnc_id": 51944,
"hgvs_c": "n.340+12900C>T",
"hgvs_p": null,
"transcript": "ENST00000770456.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000770456.1"
},
{
"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": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MIR3142HG",
"gene_hgnc_id": 51944,
"hgvs_c": "n.317+12900C>T",
"hgvs_p": null,
"transcript": "ENST00000770457.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000770457.1"
}
],
"gene_symbol": "ATP10B",
"gene_hgnc_id": 13543,
"dbsnp": "rs201409494",
"frequency_reference_population": 0.00072300085,
"hom_count_reference_population": 1,
"allele_count_reference_population": 1167,
"gnomad_exomes_af": 0.000758659,
"gnomad_genomes_af": 0.000380787,
"gnomad_exomes_ac": 1109,
"gnomad_genomes_ac": 58,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.024545997381210327,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.026,
"revel_prediction": "Benign",
"alphamissense_score": 0.0738,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.76,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.296,
"phylop100way_prediction": "Benign",
"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": -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_025153.3",
"gene_symbol": "ATP10B",
"hgnc_id": 13543,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.4346G>A",
"hgvs_p": "p.Arg1449Lys"
},
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000770454.1",
"gene_symbol": "MIR3142HG",
"hgnc_id": 51944,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.658-35216C>T",
"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
}