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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: 1-160130114-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=160130114&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 11,
"criteria": [
"PP2",
"BP4_Moderate",
"BP6",
"BS1",
"BS2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "ATP1A2",
"hgnc_id": 800,
"hgvs_c": "c.1474G>A",
"hgvs_p": "p.Glu492Lys",
"inheritance_mode": "AD,AR",
"pathogenic_score": 1,
"score": -10,
"transcript": "NM_000702.4",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "PP2,BP4_Moderate,BP6,BS1,BS2",
"acmg_score": -10,
"allele_count_reference_population": 1110,
"alphamissense_prediction": null,
"alphamissense_score": 0.2906,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Uncertain_significance",
"bayesdelnoaf_score": 0.13,
"chr": "1",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": " 2, familial hemiplegic,ATP1A2-related disorder,Alternating hemiplegia of childhood 1,Familial hemiplegic migraine,Inborn genetic diseases,Migraine,not provided,not specified",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:6 LB:4 B:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.10675838589668274,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1020,
"aa_ref": "E",
"aa_start": 492,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5435,
"cdna_start": 1577,
"cds_end": null,
"cds_length": 3063,
"cds_start": 1474,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_000702.4",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1474G>A",
"hgvs_p": "p.Glu492Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000361216.8",
"protein_coding": true,
"protein_id": "NP_000693.1",
"strand": true,
"transcript": "NM_000702.4",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1020,
"aa_ref": "E",
"aa_start": 492,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 5435,
"cdna_start": 1577,
"cds_end": null,
"cds_length": 3063,
"cds_start": 1474,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000361216.8",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1474G>A",
"hgvs_p": "p.Glu492Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000702.4",
"protein_coding": true,
"protein_id": "ENSP00000354490.3",
"strand": true,
"transcript": "ENST00000361216.8",
"transcript_support_level": 1
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1028,
"aa_ref": "E",
"aa_start": 500,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4682,
"cdna_start": 1597,
"cds_end": null,
"cds_length": 3087,
"cds_start": 1498,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000857225.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1498G>A",
"hgvs_p": "p.Glu500Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000527284.1",
"strand": true,
"transcript": "ENST00000857225.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1019,
"aa_ref": "E",
"aa_start": 492,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5433,
"cdna_start": 1578,
"cds_end": null,
"cds_length": 3060,
"cds_start": 1474,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000969831.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1474G>A",
"hgvs_p": "p.Glu492Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000639890.1",
"strand": true,
"transcript": "ENST00000969831.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1017,
"aa_ref": "E",
"aa_start": 489,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5415,
"cdna_start": 1568,
"cds_end": null,
"cds_length": 3054,
"cds_start": 1465,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000969832.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1465G>A",
"hgvs_p": "p.Glu489Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000639891.1",
"strand": true,
"transcript": "ENST00000969832.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1010,
"aa_ref": "E",
"aa_start": 482,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5405,
"cdna_start": 1543,
"cds_end": null,
"cds_length": 3033,
"cds_start": 1444,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000857224.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1444G>A",
"hgvs_p": "p.Glu482Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000527283.1",
"strand": true,
"transcript": "ENST00000857224.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 1009,
"aa_ref": "E",
"aa_start": 492,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3338,
"cdna_start": 1559,
"cds_end": null,
"cds_length": 3030,
"cds_start": 1474,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000392233.7",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1474G>A",
"hgvs_p": "p.Glu492Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000376066.3",
"strand": true,
"transcript": "ENST00000392233.7",
"transcript_support_level": 5
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 999,
"aa_ref": "E",
"aa_start": 471,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5372,
"cdna_start": 1510,
"cds_end": null,
"cds_length": 3000,
"cds_start": 1411,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000857223.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1411G>A",
"hgvs_p": "p.Glu471Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000527282.1",
"strand": true,
"transcript": "ENST00000857223.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 952,
"aa_ref": "E",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4283,
"cdna_start": 1374,
"cds_end": null,
"cds_length": 2859,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000969833.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.1270G>A",
"hgvs_p": "p.Glu424Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000639892.1",
"strand": true,
"transcript": "ENST00000969833.1",
"transcript_support_level": null
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 713,
"aa_ref": "E",
"aa_start": 202,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4413,
"cdna_start": 606,
"cds_end": null,
"cds_length": 2142,
"cds_start": 604,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000447527.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.604G>A",
"hgvs_p": "p.Glu202Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000411705.1",
"strand": true,
"transcript": "ENST00000447527.1",
"transcript_support_level": 2
},
{
"aa_alt": "K",
"aa_end": null,
"aa_length": 723,
"aa_ref": "E",
"aa_start": 195,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4451,
"cdna_start": 593,
"cds_end": null,
"cds_length": 2172,
"cds_start": 583,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "XM_047421286.1",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "c.583G>A",
"hgvs_p": "p.Glu195Lys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047277242.1",
"strand": true,
"transcript": "XM_047421286.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 3114,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 20,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000472488.5",
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"hgvs_c": "n.1577G>A",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "ENST00000472488.5",
"transcript_support_level": 2
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs142348542",
"effect": "missense_variant",
"frequency_reference_population": 0.0006876454,
"gene_hgnc_id": 800,
"gene_symbol": "ATP1A2",
"gnomad_exomes_ac": 1033,
"gnomad_exomes_af": 0.000706626,
"gnomad_exomes_homalt": 2,
"gnomad_genomes_ac": 77,
"gnomad_genomes_af": 0.000505488,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 2,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"phenotype_combined": "Familial hemiplegic migraine|Migraine, familial hemiplegic, 2|not provided|not specified|Alternating hemiplegia of childhood 1|Inborn genetic diseases|ATP1A2-related disorder",
"phylop100way_prediction": "Benign",
"phylop100way_score": 1.426,
"pos": 160130114,
"ref": "G",
"revel_prediction": "Uncertain_significance",
"revel_score": 0.519,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_000702.4"
}
]
}