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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: 14-94383044-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=94383044&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PS3",
"PP3",
"PP5_Very_Strong"
],
"effects": [
"missense_variant"
],
"gene_symbol": "SERPINA1",
"hgnc_id": 8941,
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"inheritance_mode": "AR,AD",
"pathogenic_score": 13,
"score": 13,
"transcript": "NM_000295.5",
"verdict": "Pathogenic"
}
],
"acmg_classification": "Pathogenic",
"acmg_criteria": "PS3,PP3,PP5_Very_Strong",
"acmg_score": 13,
"allele_count_reference_population": 89,
"alphamissense_prediction": null,
"alphamissense_score": 0.6761,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.28,
"chr": "14",
"clinvar_classification": "Pathogenic/Likely pathogenic",
"clinvar_disease": "Alpha-1-antitrypsin deficiency,PI M(PROCIDA),See cases,not provided",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "P:2 LP:6",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.7955477237701416,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3006,
"cdna_start": 241,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_000295.5",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000393087.9",
"protein_coding": true,
"protein_id": "NP_000286.3",
"strand": false,
"transcript": "NM_000295.5",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3006,
"cdna_start": 241,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000393087.9",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000295.5",
"protein_coding": true,
"protein_id": "ENSP00000376802.4",
"strand": false,
"transcript": "ENST00000393087.9",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3236,
"cdna_start": 471,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000355814.8",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000348068.4",
"strand": false,
"transcript": "ENST00000355814.8",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1885,
"cdna_start": 749,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000393088.8",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000376803.4",
"strand": false,
"transcript": "ENST00000393088.8",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1628,
"cdna_start": 505,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000404814.8",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000385960.4",
"strand": false,
"transcript": "ENST00000404814.8",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3340,
"cdna_start": 575,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000437397.5",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000408474.1",
"strand": false,
"transcript": "ENST00000437397.5",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3144,
"cdna_start": 379,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000440909.5",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000390299.1",
"strand": false,
"transcript": "ENST00000440909.5",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3532,
"cdna_start": 767,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000448921.5",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000416066.1",
"strand": false,
"transcript": "ENST00000448921.5",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1559,
"cdna_start": 496,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000449399.7",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000416354.3",
"strand": false,
"transcript": "ENST00000449399.7",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 359,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1450,
"cdna_start": 228,
"cds_end": null,
"cds_length": 1080,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000402629.1",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000386094.1",
"strand": false,
"transcript": "ENST00000402629.1",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 1562,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 4,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000489769.1",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "n.194T>C",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000451525.1",
"strand": false,
"transcript": "ENST00000489769.1",
"transcript_support_level": 1
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3142,
"cdna_start": 377,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001002235.3",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001002235.1",
"strand": false,
"transcript": "NM_001002235.3",
"transcript_support_level": null
},
{
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"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3456,
"cdna_start": 691,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001002236.3",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001002236.1",
"strand": false,
"transcript": "NM_001002236.3",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3179,
"cdna_start": 414,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "NM_001127700.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121172.1",
"strand": false,
"transcript": "NM_001127700.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3475,
"cdna_start": 710,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001127701.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121173.1",
"strand": false,
"transcript": "NM_001127701.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3283,
"cdna_start": 518,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001127702.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121174.1",
"strand": false,
"transcript": "NM_001127702.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3438,
"cdna_start": 673,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001127703.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121175.1",
"strand": false,
"transcript": "NM_001127703.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
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"aa_length": 418,
"aa_ref": "L",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3435,
"cdna_start": 670,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001127704.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121176.1",
"strand": false,
"transcript": "NM_001127704.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3453,
"cdna_start": 688,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 7,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001127705.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121177.1",
"strand": false,
"transcript": "NM_001127705.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3246,
"cdna_start": 481,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001127706.2",
"gene_hgnc_id": 8941,
"gene_symbol": "SERPINA1",
"hgvs_c": "c.194T>C",
"hgvs_p": "p.Leu65Pro",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001121178.1",
"strand": false,
"transcript": "NM_001127706.2",
"transcript_support_level": null
},
{
"aa_alt": "P",
"aa_end": null,
"aa_length": 418,
"aa_ref": "L",
"aa_start": 65,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3243,
"cdna_start": 478,
"cds_end": null,
"cds_length": 1257,
"cds_start": 194,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001127707.2",
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"consequences": [
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],
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"feature": "ENST00000557118.5",
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"protein_id": "ENSP00000451826.1",
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}
],
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"dbscsnv_ada_score": null,
"dbsnp": "rs28931569",
"effect": "missense_variant",
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"pathogenicity_classification_combined": "Pathogenic/Likely pathogenic",
"phenotype_combined": "PI M(PROCIDA)|Alpha-1-antitrypsin deficiency|not provided|See cases",
"phylop100way_prediction": "Benign",
"phylop100way_score": 2.619,
"pos": 94383044,
"ref": "A",
"revel_prediction": "Uncertain_significance",
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"splice_prediction_selected": "Benign",
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"splice_source_selected": "max_spliceai",
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"transcript": "NM_000295.5"
}
]
}