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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: 4-87981665-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=87981665&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 87981665,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001251830.2",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "NM_001040058.2",
"protein_id": "NP_001035147.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 314,
"cds_start": 407,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000395080.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001040058.2"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "ENST00000395080.8",
"protein_id": "ENSP00000378517.3",
"transcript_support_level": 1,
"aa_start": 136,
"aa_end": null,
"aa_length": 314,
"cds_start": 407,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001040058.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000395080.8"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.365T>C",
"hgvs_p": "p.Phe122Ser",
"transcript": "ENST00000237623.11",
"protein_id": "ENSP00000237623.7",
"transcript_support_level": 1,
"aa_start": 122,
"aa_end": null,
"aa_length": 300,
"cds_start": 365,
"cds_end": null,
"cds_length": 903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000237623.11"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.326T>C",
"hgvs_p": "p.Phe109Ser",
"transcript": "ENST00000360804.4",
"protein_id": "ENSP00000354042.4",
"transcript_support_level": 1,
"aa_start": 109,
"aa_end": null,
"aa_length": 287,
"cds_start": 326,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360804.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "n.696T>C",
"hgvs_p": null,
"transcript": "ENST00000509659.5",
"protein_id": null,
"transcript_support_level": 1,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000509659.5"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.446T>C",
"hgvs_p": "p.Phe149Ser",
"transcript": "NM_001251830.2",
"protein_id": "NP_001238759.1",
"transcript_support_level": null,
"aa_start": 149,
"aa_end": null,
"aa_length": 327,
"cds_start": 446,
"cds_end": null,
"cds_length": 984,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001251830.2"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "ENST00000614857.5",
"protein_id": "ENSP00000477824.2",
"transcript_support_level": 2,
"aa_start": 136,
"aa_end": null,
"aa_length": 314,
"cds_start": 407,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000614857.5"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "ENST00000882523.1",
"protein_id": "ENSP00000552582.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 314,
"cds_start": 407,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882523.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "ENST00000942419.1",
"protein_id": "ENSP00000612478.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 314,
"cds_start": 407,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942419.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.398T>C",
"hgvs_p": "p.Phe133Ser",
"transcript": "ENST00000882522.1",
"protein_id": "ENSP00000552581.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 311,
"cds_start": 398,
"cds_end": null,
"cds_length": 936,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882522.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.365T>C",
"hgvs_p": "p.Phe122Ser",
"transcript": "NM_000582.3",
"protein_id": "NP_000573.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 300,
"cds_start": 365,
"cds_end": null,
"cds_length": 903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000582.3"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.365T>C",
"hgvs_p": "p.Phe122Ser",
"transcript": "ENST00000942420.1",
"protein_id": "ENSP00000612479.1",
"transcript_support_level": null,
"aa_start": 122,
"aa_end": null,
"aa_length": 300,
"cds_start": 365,
"cds_end": null,
"cds_length": 903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942420.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.356T>C",
"hgvs_p": "p.Phe119Ser",
"transcript": "ENST00000882525.1",
"protein_id": "ENSP00000552584.1",
"transcript_support_level": null,
"aa_start": 119,
"aa_end": null,
"aa_length": 297,
"cds_start": 356,
"cds_end": null,
"cds_length": 894,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882525.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.350T>C",
"hgvs_p": "p.Phe117Ser",
"transcript": "ENST00000920430.1",
"protein_id": "ENSP00000590489.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 295,
"cds_start": 350,
"cds_end": null,
"cds_length": 888,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000920430.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.326T>C",
"hgvs_p": "p.Phe109Ser",
"transcript": "NM_001040060.2",
"protein_id": "NP_001035149.1",
"transcript_support_level": null,
"aa_start": 109,
"aa_end": null,
"aa_length": 287,
"cds_start": 326,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001040060.2"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.326T>C",
"hgvs_p": "p.Phe109Ser",
"transcript": "ENST00000882524.1",
"protein_id": "ENSP00000552583.1",
"transcript_support_level": null,
"aa_start": 109,
"aa_end": null,
"aa_length": 287,
"cds_start": 326,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882524.1"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.284T>C",
"hgvs_p": "p.Phe95Ser",
"transcript": "NM_001251829.2",
"protein_id": "NP_001238758.1",
"transcript_support_level": null,
"aa_start": 95,
"aa_end": null,
"aa_length": 273,
"cds_start": 284,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001251829.2"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.284T>C",
"hgvs_p": "p.Phe95Ser",
"transcript": "ENST00000508233.6",
"protein_id": "ENSP00000422973.2",
"transcript_support_level": 2,
"aa_start": 95,
"aa_end": null,
"aa_length": 273,
"cds_start": 284,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000508233.6"
},
{
"aa_ref": "F",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "c.407T>C",
"hgvs_p": "p.Phe136Ser",
"transcript": "ENST00000682655.1",
"protein_id": "ENSP00000508280.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 192,
"cds_start": 407,
"cds_end": null,
"cds_length": 579,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000682655.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "n.664T>C",
"hgvs_p": null,
"transcript": "ENST00000509334.5",
"protein_id": null,
"transcript_support_level": 5,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000509334.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "n.706T>C",
"hgvs_p": null,
"transcript": "ENST00000513981.5",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000513981.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SPP1",
"gene_hgnc_id": 11255,
"hgvs_c": "n.634T>C",
"hgvs_p": null,
"transcript": "ENST00000681973.1",
"protein_id": null,
"transcript_support_level": null,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000681973.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
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],
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"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
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"revel_prediction": "Benign",
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"bayesdelnoaf_score": -0.4,
"bayesdelnoaf_prediction": "Benign",
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"phylop100way_prediction": "Benign",
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"spliceai_max_prediction": "Benign",
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"acmg_score": 0,
"acmg_classification": "Uncertain_significance",
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"acmg_by_gene": [
{
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"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001251830.2",
"gene_symbol": "SPP1",
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"effects": [
"missense_variant"
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"inheritance_mode": "Unknown",
"hgvs_c": "c.446T>C",
"hgvs_p": "p.Phe149Ser"
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{
"score": 0,
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"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000662475.1",
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"effects": [
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],
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}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}