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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: 6-75087281-GAAA-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=75087281&ref=GAAA&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM2"
],
"effects": [
"intron_variant"
],
"gene_symbol": "COL12A1",
"hgnc_id": 2188,
"hgvs_c": "c.9181+293_9181+295delTTT",
"hgvs_p": null,
"inheritance_mode": "AD,AR",
"pathogenic_score": 2,
"score": 2,
"transcript": "NM_001424113.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_score": 2,
"allele_count_reference_population": 2,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "6",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3063,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 11725,
"cdna_start": null,
"cds_end": null,
"cds_length": 9192,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 66,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_004370.6",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9181+293_9181+295delTTT",
"hgvs_p": null,
"intron_rank": 65,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000322507.13",
"protein_coding": true,
"protein_id": "NP_004361.3",
"strand": false,
"transcript": "NM_004370.6",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3063,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 11725,
"cdna_start": null,
"cds_end": null,
"cds_length": 9192,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 66,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000322507.13",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9181+293_9181+295delTTT",
"hgvs_p": null,
"intron_rank": 65,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_004370.6",
"protein_coding": true,
"protein_id": "ENSP00000325146.8",
"strand": false,
"transcript": "ENST00000322507.13",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1899,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5886,
"cdna_start": null,
"cds_end": null,
"cds_length": 5700,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 51,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000345356.10",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.5689+293_5689+295delTTT",
"hgvs_p": null,
"intron_rank": 50,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000305147.9",
"strand": false,
"transcript": "ENST00000345356.10",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3062,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 9637,
"cdna_start": null,
"cds_end": null,
"cds_length": 9189,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 65,
"exon_rank": 65,
"exon_rank_end": null,
"feature": "ENST00000483888.6",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.*273_*275delTTT",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000421216.1",
"strand": false,
"transcript": "ENST00000483888.6",
"transcript_support_level": 5
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3118,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10533,
"cdna_start": null,
"cds_end": null,
"cds_length": 9357,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 66,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001424113.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9181+293_9181+295delTTT",
"hgvs_p": null,
"intron_rank": 65,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001411042.1",
"strand": false,
"transcript": "NM_001424113.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3056,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 11704,
"cdna_start": null,
"cds_end": null,
"cds_length": 9171,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 65,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001424114.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9160+293_9160+295delTTT",
"hgvs_p": null,
"intron_rank": 64,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001411043.1",
"strand": false,
"transcript": "NM_001424114.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 2987,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8964,
"cdna_start": null,
"cds_end": null,
"cds_length": 8964,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 63,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000416123.6",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.8953+293_8953+295delTTT",
"hgvs_p": null,
"intron_rank": 62,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000412864.2",
"strand": false,
"transcript": "ENST00000416123.6",
"transcript_support_level": 5
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 2972,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 11452,
"cdna_start": null,
"cds_end": null,
"cds_length": 8919,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 65,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001424115.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.8908+293_8908+295delTTT",
"hgvs_p": null,
"intron_rank": 64,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001411044.1",
"strand": false,
"transcript": "NM_001424115.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 2972,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10080,
"cdna_start": null,
"cds_end": null,
"cds_length": 8919,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 65,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000898574.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.8908+293_8908+295delTTT",
"hgvs_p": null,
"intron_rank": 64,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000568633.1",
"strand": false,
"transcript": "ENST00000898574.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1954,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7041,
"cdna_start": null,
"cds_end": null,
"cds_length": 5865,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 51,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_001424116.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.5689+293_5689+295delTTT",
"hgvs_p": null,
"intron_rank": 50,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001411045.1",
"strand": false,
"transcript": "NM_001424116.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1899,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8233,
"cdna_start": null,
"cds_end": null,
"cds_length": 5700,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 51,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_080645.3",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.5689+293_5689+295delTTT",
"hgvs_p": null,
"intron_rank": 50,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_542376.2",
"strand": false,
"transcript": "NM_080645.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 756,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3135,
"cdna_start": null,
"cds_end": null,
"cds_length": 2271,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 22,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000425443.6",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.2095+293_2095+295delTTT",
"hgvs_p": null,
"intron_rank": 21,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000399812.2",
"strand": false,
"transcript": "ENST00000425443.6",
"transcript_support_level": 5
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3118,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10583,
"cdna_start": null,
"cds_end": null,
"cds_length": 9357,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 66,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047418184.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9181+293_9181+295delTTT",
"hgvs_p": null,
"intron_rank": 65,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047274140.1",
"strand": false,
"transcript": "XM_047418184.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3106,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10780,
"cdna_start": null,
"cds_end": null,
"cds_length": 9321,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 65,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_017010252.3",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.9145+293_9145+295delTTT",
"hgvs_p": null,
"intron_rank": 64,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016865741.1",
"strand": false,
"transcript": "XM_017010252.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 3027,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 10260,
"cdna_start": null,
"cds_end": null,
"cds_length": 9084,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 65,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_011535435.2",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.8908+293_8908+295delTTT",
"hgvs_p": null,
"intron_rank": 64,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011533737.1",
"strand": false,
"transcript": "XM_011535435.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 1899,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8283,
"cdna_start": null,
"cds_end": null,
"cds_length": 5700,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 51,
"exon_rank": null,
"exon_rank_end": null,
"feature": "XM_047418186.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "c.5689+293_5689+295delTTT",
"hgvs_p": null,
"intron_rank": 50,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047274142.1",
"strand": false,
"transcript": "XM_047418186.1",
"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": 2782,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 4,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000680981.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "n.590+293_590+295delTTT",
"hgvs_p": null,
"intron_rank": 3,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000680981.1",
"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": 3156,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 2,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000681086.1",
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"hgvs_c": "n.964+293_964+295delTTT",
"hgvs_p": null,
"intron_rank": 1,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000681086.1",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs11289042",
"effect": "intron_variant",
"frequency_reference_population": 0.000012936611,
"gene_hgnc_id": 2188,
"gene_symbol": "COL12A1",
"gnomad_exomes_ac": 2,
"gnomad_exomes_af": 0.0000129366,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_ac": 0,
"gnomad_genomes_af": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": null,
"phenotype_combined": null,
"phylop100way_prediction": "Benign",
"phylop100way_score": 0.554,
"pos": 75087281,
"ref": "GAAA",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_001424113.1"
}
]
}