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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: 19-1912430-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=1912430&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 1912430,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_138422.4",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.383G>T",
"hgvs_p": "p.Arg128Leu",
"transcript": "NM_138422.4",
"protein_id": "NP_612431.2",
"transcript_support_level": null,
"aa_start": 128,
"aa_end": null,
"aa_length": 367,
"cds_start": 383,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 582,
"cdna_end": null,
"cdna_length": 1599,
"mane_select": "ENST00000329478.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_138422.4"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.383G>T",
"hgvs_p": "p.Arg128Leu",
"transcript": "ENST00000329478.4",
"protein_id": "ENSP00000332448.2",
"transcript_support_level": 1,
"aa_start": 128,
"aa_end": null,
"aa_length": 367,
"cds_start": 383,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 582,
"cdna_end": null,
"cdna_length": 1599,
"mane_select": "NM_138422.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000329478.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "NM_079834.4",
"protein_id": "NP_524558.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2501,
"mane_select": "ENST00000316097.13",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_079834.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000316097.13",
"protein_id": "ENSP00000316007.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2501,
"mane_select": "NM_079834.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000316097.13"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-125-5264G>T",
"hgvs_p": null,
"transcript": "ENST00000414057.6",
"protein_id": "ENSP00000479672.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 139,
"cds_start": null,
"cds_end": null,
"cds_length": 422,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1477,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000414057.6"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.383G>T",
"hgvs_p": "p.Arg128Leu",
"transcript": "ENST00000942414.1",
"protein_id": "ENSP00000612473.1",
"transcript_support_level": null,
"aa_start": 128,
"aa_end": null,
"aa_length": 367,
"cds_start": 383,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 627,
"cdna_end": null,
"cdna_length": 1636,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942414.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.383G>T",
"hgvs_p": "p.Arg128Leu",
"transcript": "ENST00000942415.1",
"protein_id": "ENSP00000612474.1",
"transcript_support_level": null,
"aa_start": 128,
"aa_end": null,
"aa_length": 367,
"cds_start": 383,
"cds_end": null,
"cds_length": 1104,
"cdna_start": 612,
"cdna_end": null,
"cdna_length": 1594,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942415.1"
},
{
"aa_ref": "R",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.335G>T",
"hgvs_p": "p.Arg112Leu",
"transcript": "NM_001329533.2",
"protein_id": "NP_001316462.1",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 351,
"cds_start": 335,
"cds_end": null,
"cds_length": 1056,
"cdna_start": 391,
"cdna_end": null,
"cdna_length": 1408,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001329533.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000873398.1",
"protein_id": "ENSP00000543457.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2520,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000873398.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "NM_001329540.2",
"protein_id": "NP_001316469.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 195,
"cds_start": null,
"cds_end": null,
"cds_length": 588,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2399,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001329540.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000409472.6",
"protein_id": "ENSP00000386865.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 195,
"cds_start": null,
"cds_end": null,
"cds_length": 588,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2584,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409472.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-125-5264G>T",
"hgvs_p": null,
"transcript": "NM_001329539.2",
"protein_id": "NP_001316468.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 185,
"cds_start": null,
"cds_end": null,
"cds_length": 558,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2453,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001329539.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000411971.5",
"protein_id": "ENSP00000388185.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 122,
"cds_start": null,
"cds_end": null,
"cds_length": 370,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 783,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000411971.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "c.-126+3795G>T",
"hgvs_p": null,
"transcript": "ENST00000588907.2",
"protein_id": "ENSP00000478264.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 21,
"cds_start": null,
"cds_end": null,
"cds_length": 67,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 547,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000588907.2"
},
{
"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": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "n.69-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000452128.6",
"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": 718,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000452128.6"
},
{
"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": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "n.-41-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000460767.5",
"protein_id": "ENSP00000481989.1",
"transcript_support_level": 4,
"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": 569,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000460767.5"
},
{
"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": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SCAMP4",
"gene_hgnc_id": 30385,
"hgvs_c": "n.42-2549G>T",
"hgvs_p": null,
"transcript": "ENST00000489554.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 573,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000489554.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"hgvs_c": "c.*175G>T",
"hgvs_p": null,
"transcript": "ENST00000454697.1",
"protein_id": "ENSP00000404502.2",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 68,
"cds_start": null,
"cds_end": null,
"cds_length": 208,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 983,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000454697.1"
}
],
"gene_symbol": "ADAT3",
"gene_hgnc_id": 25151,
"dbsnp": "rs200992550",
"frequency_reference_population": 0.0021763672,
"hom_count_reference_population": 4,
"allele_count_reference_population": 3289,
"gnomad_exomes_af": 0.00216703,
"gnomad_genomes_af": 0.00225977,
"gnomad_exomes_ac": 2945,
"gnomad_genomes_ac": 344,
"gnomad_exomes_homalt": 4,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0057032108306884766,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.055,
"revel_prediction": "Benign",
"alphamissense_score": 0.0649,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.63,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.191,
"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": -9,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BS2",
"acmg_by_gene": [
{
"score": -9,
"benign_score": 9,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_138422.4",
"gene_symbol": "ADAT3",
"hgnc_id": 25151,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.383G>T",
"hgvs_p": "p.Arg128Leu"
},
{
"score": -9,
"benign_score": 9,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_079834.4",
"gene_symbol": "SCAMP4",
"hgnc_id": 30385,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.-41-2549G>T",
"hgvs_p": null
}
],
"clinvar_disease": "ADAT3-related disorder,Inborn genetic diseases,not provided,not specified",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:1 LB:4 B:1",
"phenotype_combined": "not specified|not provided|Inborn genetic diseases|ADAT3-related disorder",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}