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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: 6-148520616-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=148520616&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 148520616,
"ref": "T",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000367467.8",
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1209+723T>C",
"hgvs_p": null,
"transcript": "NM_015278.5",
"protein_id": "NP_056093.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1247,
"cds_start": -4,
"cds_end": null,
"cds_length": 3744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7460,
"mane_select": "ENST00000367467.8",
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1209+723T>C",
"hgvs_p": null,
"transcript": "ENST00000367467.8",
"protein_id": "ENSP00000356437.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1247,
"cds_start": -4,
"cds_end": null,
"cds_length": 3744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7460,
"mane_select": "NM_015278.5",
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1074+723T>C",
"hgvs_p": null,
"transcript": "NM_001346505.2",
"protein_id": "NP_001333434.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1202,
"cds_start": -4,
"cds_end": null,
"cds_length": 3609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7124,
"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": 13,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.981+234T>C",
"hgvs_p": null,
"transcript": "NM_001346508.2",
"protein_id": "NP_001333437.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1171,
"cds_start": -4,
"cds_end": null,
"cds_length": 3516,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7369,
"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": 13,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.858+234T>C",
"hgvs_p": null,
"transcript": "NM_001346509.2",
"protein_id": "NP_001333438.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1130,
"cds_start": -4,
"cds_end": null,
"cds_length": 3393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7177,
"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": 21,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.837+723T>C",
"hgvs_p": null,
"transcript": "NM_001346506.2",
"protein_id": "NP_001333435.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1123,
"cds_start": -4,
"cds_end": null,
"cds_length": 3372,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7525,
"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": 13,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.492+723T>C",
"hgvs_p": null,
"transcript": "NM_001346507.2",
"protein_id": "NP_001333436.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1008,
"cds_start": -4,
"cds_end": null,
"cds_length": 3027,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6880,
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.969+234T>C",
"hgvs_p": null,
"transcript": "ENST00000636279.1",
"protein_id": "ENSP00000490865.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 358,
"cds_start": -4,
"cds_end": null,
"cds_length": 1077,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1077,
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1698+234T>C",
"hgvs_p": null,
"transcript": "XM_017010598.3",
"protein_id": "XP_016866087.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1410,
"cds_start": -4,
"cds_end": null,
"cds_length": 4233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7949,
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1587+234T>C",
"hgvs_p": null,
"transcript": "XM_017010599.2",
"protein_id": "XP_016866088.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1373,
"cds_start": -4,
"cds_end": null,
"cds_length": 4122,
"cdna_start": null,
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"cdna_length": 7721,
"mane_select": null,
"mane_plus": null,
"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": 20,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1563+234T>C",
"hgvs_p": null,
"transcript": "XM_017010600.2",
"protein_id": "XP_016866089.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 1365,
"cds_start": -4,
"cds_end": null,
"cds_length": 4098,
"cdna_start": null,
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"cdna_length": 7613,
"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,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": 8,
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"gene_symbol": "SASH1",
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"hgvs_c": "c.1419+234T>C",
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"transcript": "XM_047418496.1",
"protein_id": "XP_047274452.1",
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},
{
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"intron_variant"
],
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"exon_count": 18,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1419+234T>C",
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"transcript": "XM_047418497.1",
"protein_id": "XP_047274453.1",
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
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"intron_variant"
],
"exon_rank": null,
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"exon_count": 18,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1326+234T>C",
"hgvs_p": null,
"transcript": "XM_017010605.2",
"protein_id": "XP_016866094.1",
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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": 17,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1203+234T>C",
"hgvs_p": null,
"transcript": "XM_047418498.1",
"protein_id": "XP_047274454.1",
"transcript_support_level": null,
"aa_start": null,
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"feature": null
},
{
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"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 7,
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"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.1203+234T>C",
"hgvs_p": null,
"transcript": "XM_047418499.1",
"protein_id": "XP_047274455.1",
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},
{
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],
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"gene_symbol": "SASH1",
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"hgvs_c": "c.1098+723T>C",
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"transcript": "XM_024446384.2",
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"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
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"exon_count": 13,
"intron_rank": 3,
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"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.972+234T>C",
"hgvs_p": null,
"transcript": "XM_024446385.2",
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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": 20,
"intron_rank": 10,
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"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"hgvs_c": "c.969+723T>C",
"hgvs_p": null,
"transcript": "XM_047418500.1",
"protein_id": "XP_047274456.1",
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}
],
"gene_symbol": "SASH1",
"gene_hgnc_id": 19182,
"dbsnp": "rs1147857",
"frequency_reference_population": 0.45466217,
"hom_count_reference_population": 16680,
"allele_count_reference_population": 69055,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.454662,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 69055,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 16680,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8199999928474426,
"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": -0.82,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.862,
"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": "ENST00000367467.8",
"gene_symbol": "SASH1",
"hgnc_id": 19182,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.1209+723T>C",
"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
}