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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: 22-25774660-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=25774660&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 25774660,
"ref": "C",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000407587.6",
"consequences": [
{
"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": 44,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "NM_032608.7",
"protein_id": "NP_115997.5",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2567,
"cds_start": -4,
"cds_end": null,
"cds_length": 7704,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8534,
"mane_select": "ENST00000335473.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 44,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "ENST00000335473.12",
"protein_id": "ENSP00000334563.8",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2567,
"cds_start": -4,
"cds_end": null,
"cds_length": 7704,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8534,
"mane_select": "NM_032608.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 44,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "ENST00000407587.6",
"protein_id": "ENSP00000386096.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2568,
"cds_start": -4,
"cds_end": null,
"cds_length": 7707,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8090,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 43,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "ENST00000536101.5",
"protein_id": "ENSP00000441229.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2567,
"cds_start": -4,
"cds_end": null,
"cds_length": 7704,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8051,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 39,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "n.440+2150C>T",
"hgvs_p": null,
"transcript": "ENST00000418374.6",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6363,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "n.1869+2150C>T",
"hgvs_p": null,
"transcript": "ENST00000539302.5",
"protein_id": "ENSP00000437587.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7774,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 44,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "NM_001318245.2",
"protein_id": "NP_001305174.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2568,
"cds_start": -4,
"cds_end": null,
"cds_length": 7707,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8537,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 45,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530458.3",
"protein_id": "XP_011528760.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2610,
"cds_start": -4,
"cds_end": null,
"cds_length": 7833,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8663,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 45,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530459.3",
"protein_id": "XP_011528761.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2610,
"cds_start": -4,
"cds_end": null,
"cds_length": 7833,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8688,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 44,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530460.3",
"protein_id": "XP_011528762.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2610,
"cds_start": -4,
"cds_end": null,
"cds_length": 7833,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8561,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 45,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530461.3",
"protein_id": "XP_011528763.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"mane_select": null,
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"biotype": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 45,
"intron_rank": 8,
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"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_017029013.2",
"protein_id": "XP_016884502.1",
"transcript_support_level": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530464.3",
"protein_id": "XP_011528766.1",
"transcript_support_level": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 45,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_017029014.2",
"protein_id": "XP_016884503.1",
"transcript_support_level": null,
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"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
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"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_047441551.1",
"protein_id": "XP_047297507.1",
"transcript_support_level": null,
"aa_start": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 7,
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"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null,
"transcript": "XM_017029015.2",
"protein_id": "XP_016884504.1",
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},
{
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"strand": true,
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"intron_variant"
],
"exon_rank": null,
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"exon_count": 44,
"intron_rank": 7,
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"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1512+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530465.3",
"protein_id": "XP_011528767.1",
"transcript_support_level": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 41,
"intron_rank": 8,
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"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"hgvs_c": "c.1995+2150C>T",
"hgvs_p": null,
"transcript": "XM_011530466.3",
"protein_id": "XP_011528768.1",
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"feature": null
}
],
"gene_symbol": "MYO18B",
"gene_hgnc_id": 18150,
"dbsnp": "rs9624894",
"frequency_reference_population": 0.2886671,
"hom_count_reference_population": 6805,
"allele_count_reference_population": 43908,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.288667,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 43908,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 6805,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8299999833106995,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.83,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.99,
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000407587.6",
"gene_symbol": "MYO18B",
"hgnc_id": 18150,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1869+2150C>T",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}