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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: 2-96707784-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=96707784&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 96707784,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001142292.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.834A>T",
"hgvs_p": "p.Arg278Ser",
"transcript": "NM_030805.4",
"protein_id": "NP_110432.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 348,
"cds_start": 834,
"cds_end": null,
"cds_length": 1047,
"cdna_start": 858,
"cdna_end": null,
"cdna_length": 2398,
"mane_select": "ENST00000264963.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_030805.4"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.834A>T",
"hgvs_p": "p.Arg278Ser",
"transcript": "ENST00000264963.9",
"protein_id": "ENSP00000264963.4",
"transcript_support_level": 1,
"aa_start": 278,
"aa_end": null,
"aa_length": 348,
"cds_start": 834,
"cds_end": null,
"cds_length": 1047,
"cdna_start": 858,
"cdna_end": null,
"cdna_length": 2398,
"mane_select": "NM_030805.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000264963.9"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.867A>T",
"hgvs_p": "p.Arg289Ser",
"transcript": "ENST00000377079.8",
"protein_id": "ENSP00000366280.4",
"transcript_support_level": 1,
"aa_start": 289,
"aa_end": null,
"aa_length": 359,
"cds_start": 867,
"cds_end": null,
"cds_length": 1080,
"cdna_start": 891,
"cdna_end": null,
"cdna_length": 2020,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000377079.8"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.873A>T",
"hgvs_p": "p.Arg291Ser",
"transcript": "ENST00000970314.1",
"protein_id": "ENSP00000640373.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 361,
"cds_start": 873,
"cds_end": null,
"cds_length": 1086,
"cdna_start": 897,
"cdna_end": null,
"cdna_length": 2434,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970314.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.867A>T",
"hgvs_p": "p.Arg289Ser",
"transcript": "NM_001142292.2",
"protein_id": "NP_001135764.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 359,
"cds_start": 867,
"cds_end": null,
"cds_length": 1080,
"cdna_start": 891,
"cdna_end": null,
"cdna_length": 2431,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001142292.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.840A>T",
"hgvs_p": "p.Arg280Ser",
"transcript": "ENST00000893541.1",
"protein_id": "ENSP00000563600.1",
"transcript_support_level": null,
"aa_start": 280,
"aa_end": null,
"aa_length": 350,
"cds_start": 840,
"cds_end": null,
"cds_length": 1053,
"cdna_start": 864,
"cdna_end": null,
"cdna_length": 2404,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893541.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.831A>T",
"hgvs_p": "p.Arg277Ser",
"transcript": "ENST00000970312.1",
"protein_id": "ENSP00000640371.1",
"transcript_support_level": null,
"aa_start": 277,
"aa_end": null,
"aa_length": 347,
"cds_start": 831,
"cds_end": null,
"cds_length": 1044,
"cdna_start": 861,
"cdna_end": null,
"cdna_length": 3337,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970312.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.867A>T",
"hgvs_p": "p.Arg289Ser",
"transcript": "ENST00000970313.1",
"protein_id": "ENSP00000640372.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 331,
"cds_start": 867,
"cds_end": null,
"cds_length": 996,
"cdna_start": 911,
"cdna_end": null,
"cdna_length": 2364,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970313.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.762A>T",
"hgvs_p": "p.Arg254Ser",
"transcript": "ENST00000970315.1",
"protein_id": "ENSP00000640374.1",
"transcript_support_level": null,
"aa_start": 254,
"aa_end": null,
"aa_length": 324,
"cds_start": 762,
"cds_end": null,
"cds_length": 975,
"cdna_start": 786,
"cdna_end": null,
"cdna_length": 2321,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970315.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.834A>T",
"hgvs_p": "p.Arg278Ser",
"transcript": "ENST00000920371.1",
"protein_id": "ENSP00000590430.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 320,
"cds_start": 834,
"cds_end": null,
"cds_length": 963,
"cdna_start": 858,
"cdna_end": null,
"cdna_length": 2314,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000920371.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.729A>T",
"hgvs_p": "p.Arg243Ser",
"transcript": "ENST00000893540.1",
"protein_id": "ENSP00000563599.1",
"transcript_support_level": null,
"aa_start": 243,
"aa_end": null,
"aa_length": 313,
"cds_start": 729,
"cds_end": null,
"cds_length": 942,
"cdna_start": 766,
"cdna_end": null,
"cdna_length": 2306,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893540.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.672A>T",
"hgvs_p": "p.Arg224Ser",
"transcript": "ENST00000893542.1",
"protein_id": "ENSP00000563601.1",
"transcript_support_level": null,
"aa_start": 224,
"aa_end": null,
"aa_length": 294,
"cds_start": 672,
"cds_end": null,
"cds_length": 885,
"cdna_start": 696,
"cdna_end": null,
"cdna_length": 2233,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893542.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.453A>T",
"hgvs_p": "p.Arg151Ser",
"transcript": "NM_001322347.2",
"protein_id": "NP_001309276.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 221,
"cds_start": 453,
"cds_end": null,
"cds_length": 666,
"cdna_start": 772,
"cdna_end": null,
"cdna_length": 2312,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322347.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.453A>T",
"hgvs_p": "p.Arg151Ser",
"transcript": "NM_001322352.2",
"protein_id": "NP_001309281.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 221,
"cds_start": 453,
"cds_end": null,
"cds_length": 666,
"cdna_start": 972,
"cdna_end": null,
"cdna_length": 2512,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322352.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.432A>T",
"hgvs_p": "p.Arg144Ser",
"transcript": "NM_001322346.2",
"protein_id": "NP_001309275.1",
"transcript_support_level": null,
"aa_start": 144,
"aa_end": null,
"aa_length": 214,
"cds_start": 432,
"cds_end": null,
"cds_length": 645,
"cdna_start": 808,
"cdna_end": null,
"cdna_length": 2348,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322346.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.432A>T",
"hgvs_p": "p.Arg144Ser",
"transcript": "NM_001322354.2",
"protein_id": "NP_001309283.1",
"transcript_support_level": null,
"aa_start": 144,
"aa_end": null,
"aa_length": 214,
"cds_start": 432,
"cds_end": null,
"cds_length": 645,
"cdna_start": 822,
"cdna_end": null,
"cdna_length": 2362,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322354.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.420A>T",
"hgvs_p": "p.Arg140Ser",
"transcript": "NM_001322350.2",
"protein_id": "NP_001309279.1",
"transcript_support_level": null,
"aa_start": 140,
"aa_end": null,
"aa_length": 210,
"cds_start": 420,
"cds_end": null,
"cds_length": 633,
"cdna_start": 739,
"cdna_end": null,
"cdna_length": 2279,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322350.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.399A>T",
"hgvs_p": "p.Arg133Ser",
"transcript": "NM_001322351.2",
"protein_id": "NP_001309280.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 203,
"cds_start": 399,
"cds_end": null,
"cds_length": 612,
"cdna_start": 656,
"cdna_end": null,
"cdna_length": 2196,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322351.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.399A>T",
"hgvs_p": "p.Arg133Ser",
"transcript": "NM_001322355.2",
"protein_id": "NP_001309284.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 203,
"cds_start": 399,
"cds_end": null,
"cds_length": 612,
"cdna_start": 856,
"cdna_end": null,
"cdna_length": 2396,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322355.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.399A>T",
"hgvs_p": "p.Arg133Ser",
"transcript": "NM_001322356.2",
"protein_id": "NP_001309285.1",
"transcript_support_level": null,
"aa_start": 133,
"aa_end": null,
"aa_length": 203,
"cds_start": 399,
"cds_end": null,
"cds_length": 612,
"cdna_start": 775,
"cdna_end": null,
"cdna_length": 2315,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322356.2"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "c.420A>T",
"hgvs_p": "p.Arg140Ser",
"transcript": "XM_047445946.1",
"protein_id": "XP_047301902.1",
"transcript_support_level": null,
"aa_start": 140,
"aa_end": null,
"aa_length": 210,
"cds_start": 420,
"cds_end": null,
"cds_length": 633,
"cdna_start": 699,
"cdna_end": null,
"cdna_length": 2239,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047445946.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LMAN2L",
"gene_hgnc_id": 19263,
"hgvs_c": "n.*591A>T",
"hgvs_p": null,
"transcript": "ENST00000434524.5",
"protein_id": "ENSP00000413533.1",
"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": 2410,
"mane_select": null,
"mane_plus": null,
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],
"gene_symbol": "LMAN2L",
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"hom_count_reference_population": 0,
"allele_count_reference_population": 4,
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"gnomad_genomes_ac": 2,
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"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.45715245604515076,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.319,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.6748,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.25,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.187,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
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"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
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"acmg_score": 2,
"acmg_classification": "Uncertain_significance",
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"acmg_by_gene": [
{
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"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
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],
"verdict": "Uncertain_significance",
"transcript": "NM_001142292.2",
"gene_symbol": "LMAN2L",
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"effects": [
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],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.867A>T",
"hgvs_p": "p.Arg289Ser"
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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
}