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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: 1-160135250-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=160135250&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 160135250,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "NM_000702.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2070G>A",
"hgvs_p": "p.Thr690Thr",
"transcript": "NM_000702.4",
"protein_id": "NP_000693.1",
"transcript_support_level": null,
"aa_start": 690,
"aa_end": null,
"aa_length": 1020,
"cds_start": 2070,
"cds_end": null,
"cds_length": 3063,
"cdna_start": 2173,
"cdna_end": null,
"cdna_length": 5435,
"mane_select": "ENST00000361216.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000702.4"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2070G>A",
"hgvs_p": "p.Thr690Thr",
"transcript": "ENST00000361216.8",
"protein_id": "ENSP00000354490.3",
"transcript_support_level": 1,
"aa_start": 690,
"aa_end": null,
"aa_length": 1020,
"cds_start": 2070,
"cds_end": null,
"cds_length": 3063,
"cdna_start": 2173,
"cdna_end": null,
"cdna_length": 5435,
"mane_select": "NM_000702.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000361216.8"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2094G>A",
"hgvs_p": "p.Thr698Thr",
"transcript": "ENST00000857225.1",
"protein_id": "ENSP00000527284.1",
"transcript_support_level": null,
"aa_start": 698,
"aa_end": null,
"aa_length": 1028,
"cds_start": 2094,
"cds_end": null,
"cds_length": 3087,
"cdna_start": 2193,
"cdna_end": null,
"cdna_length": 4682,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857225.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2070G>A",
"hgvs_p": "p.Thr690Thr",
"transcript": "ENST00000969831.1",
"protein_id": "ENSP00000639890.1",
"transcript_support_level": null,
"aa_start": 690,
"aa_end": null,
"aa_length": 1019,
"cds_start": 2070,
"cds_end": null,
"cds_length": 3060,
"cdna_start": 2174,
"cdna_end": null,
"cdna_length": 5433,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969831.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2061G>A",
"hgvs_p": "p.Thr687Thr",
"transcript": "ENST00000969832.1",
"protein_id": "ENSP00000639891.1",
"transcript_support_level": null,
"aa_start": 687,
"aa_end": null,
"aa_length": 1017,
"cds_start": 2061,
"cds_end": null,
"cds_length": 3054,
"cdna_start": 2164,
"cdna_end": null,
"cdna_length": 5415,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969832.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2040G>A",
"hgvs_p": "p.Thr680Thr",
"transcript": "ENST00000857224.1",
"protein_id": "ENSP00000527283.1",
"transcript_support_level": null,
"aa_start": 680,
"aa_end": null,
"aa_length": 1010,
"cds_start": 2040,
"cds_end": null,
"cds_length": 3033,
"cdna_start": 2139,
"cdna_end": null,
"cdna_length": 5405,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857224.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2070G>A",
"hgvs_p": "p.Thr690Thr",
"transcript": "ENST00000392233.7",
"protein_id": "ENSP00000376066.3",
"transcript_support_level": 5,
"aa_start": 690,
"aa_end": null,
"aa_length": 1009,
"cds_start": 2070,
"cds_end": null,
"cds_length": 3030,
"cdna_start": 2155,
"cdna_end": null,
"cdna_length": 3338,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392233.7"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2007G>A",
"hgvs_p": "p.Thr669Thr",
"transcript": "ENST00000857223.1",
"protein_id": "ENSP00000527282.1",
"transcript_support_level": null,
"aa_start": 669,
"aa_end": null,
"aa_length": 999,
"cds_start": 2007,
"cds_end": null,
"cds_length": 3000,
"cdna_start": 2106,
"cdna_end": null,
"cdna_length": 5372,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857223.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.1866G>A",
"hgvs_p": "p.Thr622Thr",
"transcript": "ENST00000969833.1",
"protein_id": "ENSP00000639892.1",
"transcript_support_level": null,
"aa_start": 622,
"aa_end": null,
"aa_length": 952,
"cds_start": 1866,
"cds_end": null,
"cds_length": 2859,
"cdna_start": 1970,
"cdna_end": null,
"cdna_length": 4283,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969833.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.1200G>A",
"hgvs_p": "p.Thr400Thr",
"transcript": "ENST00000447527.1",
"protein_id": "ENSP00000411705.1",
"transcript_support_level": 2,
"aa_start": 400,
"aa_end": null,
"aa_length": 713,
"cds_start": 1200,
"cds_end": null,
"cds_length": 2142,
"cdna_start": 1202,
"cdna_end": null,
"cdna_length": 4413,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000447527.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.1179G>A",
"hgvs_p": "p.Thr393Thr",
"transcript": "XM_047421286.1",
"protein_id": "XP_047277242.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 723,
"cds_start": 1179,
"cds_end": null,
"cds_length": 2172,
"cdna_start": 1189,
"cdna_end": null,
"cdna_length": 4451,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047421286.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "n.2173G>A",
"hgvs_p": null,
"transcript": "ENST00000472488.5",
"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": 3114,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000472488.5"
}
],
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"dbsnp": "rs142865268",
"frequency_reference_population": 0.00009293519,
"hom_count_reference_population": 0,
"allele_count_reference_population": 150,
"gnomad_exomes_af": 0.0000950824,
"gnomad_genomes_af": 0.0000723028,
"gnomad_exomes_ac": 139,
"gnomad_genomes_ac": 11,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.020999999716877937,
"computational_prediction_selected": "Benign",
"computational_source_selected": "REVEL",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.021,
"revel_prediction": "Benign",
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.68,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.888,
"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": -15,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BS1",
"acmg_by_gene": [
{
"score": -15,
"benign_score": 15,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6_Very_Strong",
"BP7",
"BS1"
],
"verdict": "Benign",
"transcript": "NM_000702.4",
"gene_symbol": "ATP1A2",
"hgnc_id": 800,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.2070G>A",
"hgvs_p": "p.Thr690Thr"
}
],
"clinvar_disease": "Familial hemiplegic migraine,Inborn genetic diseases,not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3",
"phenotype_combined": "Familial hemiplegic migraine|not provided|Inborn genetic diseases",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}