← 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: 1-160139735-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=160139735&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 160139735,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_000702.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2936C>T",
"hgvs_p": "p.Pro979Leu",
"transcript": "NM_000702.4",
"protein_id": "NP_000693.1",
"transcript_support_level": null,
"aa_start": 979,
"aa_end": null,
"aa_length": 1020,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3063,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000361216.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000702.4"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2936C>T",
"hgvs_p": "p.Pro979Leu",
"transcript": "ENST00000361216.8",
"protein_id": "ENSP00000354490.3",
"transcript_support_level": 1,
"aa_start": 979,
"aa_end": null,
"aa_length": 1020,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3063,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000702.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000361216.8"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2960C>T",
"hgvs_p": "p.Pro987Leu",
"transcript": "ENST00000857225.1",
"protein_id": "ENSP00000527284.1",
"transcript_support_level": null,
"aa_start": 987,
"aa_end": null,
"aa_length": 1028,
"cds_start": 2960,
"cds_end": null,
"cds_length": 3087,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857225.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2936C>T",
"hgvs_p": "p.Pro979Leu",
"transcript": "ENST00000969831.1",
"protein_id": "ENSP00000639890.1",
"transcript_support_level": null,
"aa_start": 979,
"aa_end": null,
"aa_length": 1019,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3060,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969831.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2927C>T",
"hgvs_p": "p.Pro976Leu",
"transcript": "ENST00000969832.1",
"protein_id": "ENSP00000639891.1",
"transcript_support_level": null,
"aa_start": 976,
"aa_end": null,
"aa_length": 1017,
"cds_start": 2927,
"cds_end": null,
"cds_length": 3054,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969832.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2906C>T",
"hgvs_p": "p.Pro969Leu",
"transcript": "ENST00000857224.1",
"protein_id": "ENSP00000527283.1",
"transcript_support_level": null,
"aa_start": 969,
"aa_end": null,
"aa_length": 1010,
"cds_start": 2906,
"cds_end": null,
"cds_length": 3033,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857224.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2936C>T",
"hgvs_p": "p.Pro979Leu",
"transcript": "ENST00000392233.7",
"protein_id": "ENSP00000376066.3",
"transcript_support_level": 5,
"aa_start": 979,
"aa_end": null,
"aa_length": 1009,
"cds_start": 2936,
"cds_end": null,
"cds_length": 3030,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392233.7"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2873C>T",
"hgvs_p": "p.Pro958Leu",
"transcript": "ENST00000857223.1",
"protein_id": "ENSP00000527282.1",
"transcript_support_level": null,
"aa_start": 958,
"aa_end": null,
"aa_length": 999,
"cds_start": 2873,
"cds_end": null,
"cds_length": 3000,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000857223.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2732C>T",
"hgvs_p": "p.Pro911Leu",
"transcript": "ENST00000969833.1",
"protein_id": "ENSP00000639892.1",
"transcript_support_level": null,
"aa_start": 911,
"aa_end": null,
"aa_length": 952,
"cds_start": 2732,
"cds_end": null,
"cds_length": 2859,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000969833.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2015C>T",
"hgvs_p": "p.Pro672Leu",
"transcript": "ENST00000447527.1",
"protein_id": "ENSP00000411705.1",
"transcript_support_level": 2,
"aa_start": 672,
"aa_end": null,
"aa_length": 713,
"cds_start": 2015,
"cds_end": null,
"cds_length": 2142,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000447527.1"
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "c.2045C>T",
"hgvs_p": "p.Pro682Leu",
"transcript": "XM_047421286.1",
"protein_id": "XP_047277242.1",
"transcript_support_level": null,
"aa_start": 682,
"aa_end": null,
"aa_length": 723,
"cds_start": 2045,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"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": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "n.272C>T",
"hgvs_p": null,
"transcript": "ENST00000463989.1",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000463989.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"hgvs_c": "n.-224C>T",
"hgvs_p": null,
"transcript": "ENST00000459972.1",
"protein_id": null,
"transcript_support_level": 5,
"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": "ENST00000459972.1"
}
],
"gene_symbol": "ATP1A2",
"gene_hgnc_id": 800,
"dbsnp": "rs121918615",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9623487591743469,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.949,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.955,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.57,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.905,
"phylop100way_prediction": "Pathogenic",
"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": 17,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PM2,PM5,PP2,PP3_Strong,PP5_Very_Strong",
"acmg_by_gene": [
{
"score": 17,
"benign_score": 0,
"pathogenic_score": 17,
"criteria": [
"PM2",
"PM5",
"PP2",
"PP3_Strong",
"PP5_Very_Strong"
],
"verdict": "Pathogenic",
"transcript": "NM_000702.4",
"gene_symbol": "ATP1A2",
"hgnc_id": 800,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.2936C>T",
"hgvs_p": "p.Pro979Leu"
}
],
"clinvar_disease": " 2, familial hemiplegic,Alternating hemiplegia of childhood 1,Familial hemiplegic migraine,Migraine,not provided",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:3 O:2",
"phenotype_combined": "Migraine, familial hemiplegic, 2|Familial hemiplegic migraine|Migraine, familial hemiplegic, 2;Alternating hemiplegia of childhood 1|not provided",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}