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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: 22-50092222-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=50092222&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 50092222,
"ref": "G",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000262794.10",
"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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "NM_018995.3",
"protein_id": "NP_061868.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1211,
"cds_start": -4,
"cds_end": null,
"cds_length": 3636,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3957,
"mane_select": "ENST00000262794.10",
"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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "ENST00000262794.10",
"protein_id": "ENSP00000262794.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1211,
"cds_start": -4,
"cds_end": null,
"cds_length": 3636,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3957,
"mane_select": "NM_018995.3",
"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": 26,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "ENST00000395858.7",
"protein_id": "ENSP00000379199.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1165,
"cds_start": -4,
"cds_end": null,
"cds_length": 3498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3763,
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "n.*438+37G>T",
"hgvs_p": null,
"transcript": "ENST00000395854.6",
"protein_id": "ENSP00000379195.2",
"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": 1044,
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "n.*1388+37G>T",
"hgvs_p": null,
"transcript": "ENST00000419054.5",
"protein_id": "ENSP00000410957.1",
"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": 2003,
"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": 26,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "NM_001164104.2",
"protein_id": "NP_001157576.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1165,
"cds_start": -4,
"cds_end": null,
"cds_length": 3498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3819,
"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": 26,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.222+37G>T",
"hgvs_p": null,
"transcript": "NM_001164105.2",
"protein_id": "NP_001157577.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1165,
"cds_start": -4,
"cds_end": null,
"cds_length": 3498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4192,
"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": 26,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.222+37G>T",
"hgvs_p": null,
"transcript": "ENST00000540615.5",
"protein_id": "ENSP00000438542.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 1165,
"cds_start": -4,
"cds_end": null,
"cds_length": 3498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3941,
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "n.327+37G>T",
"hgvs_p": null,
"transcript": "ENST00000475190.1",
"protein_id": null,
"transcript_support_level": 4,
"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": 536,
"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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_011530696.2",
"protein_id": "XP_011528998.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1256,
"cds_start": -4,
"cds_end": null,
"cds_length": 3771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4092,
"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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.222+37G>T",
"hgvs_p": null,
"transcript": "XM_011530697.2",
"protein_id": "XP_011528999.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1236,
"cds_start": -4,
"cds_end": null,
"cds_length": 3711,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4419,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_017028833.2",
"protein_id": "XP_016884322.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 1210,
"cds_start": -4,
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"cds_length": 3633,
"cdna_start": null,
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"cdna_length": 3954,
"mane_select": 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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_011530698.2",
"protein_id": "XP_011529000.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1209,
"cds_start": -4,
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"cds_length": 3630,
"cdna_start": null,
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"cdna_length": 3951,
"mane_select": 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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.126+37G>T",
"hgvs_p": null,
"transcript": "XM_011530699.2",
"protein_id": "XP_011529001.1",
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"aa_start": 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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.126+37G>T",
"hgvs_p": null,
"transcript": "XM_011530700.3",
"protein_id": "XP_011529002.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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"mane_select": 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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.222+37G>T",
"hgvs_p": null,
"transcript": "XM_005261923.5",
"protein_id": "XP_005261980.1",
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"aa_start": null,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 24,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_011530701.1",
"protein_id": "XP_011529003.1",
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"cdna_start": null,
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"cdna_length": 3390,
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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": 24,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.-282+37G>T",
"hgvs_p": null,
"transcript": "XM_047441413.1",
"protein_id": "XP_047297369.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 924,
"cds_start": -4,
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"cdna_start": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 20,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
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"transcript": "XM_047441414.1",
"protein_id": "XP_047297370.1",
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},
{
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"strand": true,
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],
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"intron_rank": 2,
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"gene_symbol": "MOV10L1",
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"hgvs_c": "c.282+37G>T",
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"transcript": "XM_017028834.2",
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"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_011530704.1",
"protein_id": "XP_011529006.1",
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"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": 13,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"hgvs_c": "c.282+37G>T",
"hgvs_p": null,
"transcript": "XM_017028837.1",
"protein_id": "XP_016884326.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 611,
"cds_start": -4,
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"cds_length": 1836,
"cdna_start": null,
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"cdna_length": 3230,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MOV10L1",
"gene_hgnc_id": 7201,
"dbsnp": "rs738490",
"frequency_reference_population": 0.0000014042163,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000140422,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -1.0299999713897705,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -1.03,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.309,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000262794.10",
"gene_symbol": "MOV10L1",
"hgnc_id": 7201,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.282+37G>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
}