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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: 7-128767546-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=128767546&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 128767546,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001199671.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "NM_001219.5",
"protein_id": "NP_001210.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 819,
"cdna_end": null,
"cdna_length": 5266,
"mane_select": "ENST00000249364.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001219.5"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000249364.9",
"protein_id": "ENSP00000249364.4",
"transcript_support_level": 1,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 819,
"cdna_end": null,
"cdna_length": 5266,
"mane_select": "NM_001219.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000249364.9"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.758G>A",
"hgvs_p": "p.Arg253His",
"transcript": "ENST00000479257.5",
"protein_id": "ENSP00000420381.1",
"transcript_support_level": 1,
"aa_start": 253,
"aa_end": null,
"aa_length": 323,
"cds_start": 758,
"cds_end": null,
"cds_length": 972,
"cdna_start": 1589,
"cdna_end": null,
"cdna_length": 2572,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000479257.5"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.758G>A",
"hgvs_p": "p.Arg253His",
"transcript": "ENST00000542996.7",
"protein_id": "ENSP00000438248.1",
"transcript_support_level": 1,
"aa_start": 253,
"aa_end": null,
"aa_length": 323,
"cds_start": 758,
"cds_end": null,
"cds_length": 972,
"cdna_start": 1634,
"cdna_end": null,
"cdna_length": 6081,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000542996.7"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000449187.7",
"protein_id": "ENSP00000408838.2",
"transcript_support_level": 1,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 819,
"cdna_end": null,
"cdna_length": 5266,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000449187.7"
},
{
"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": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.644-1517G>A",
"hgvs_p": null,
"transcript": "ENST00000535011.6",
"protein_id": "ENSP00000442110.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 224,
"cds_start": null,
"cds_end": null,
"cds_length": 675,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3210,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000535011.6"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.917G>A",
"hgvs_p": "p.Arg306His",
"transcript": "ENST00000955247.1",
"protein_id": "ENSP00000625306.1",
"transcript_support_level": null,
"aa_start": 306,
"aa_end": null,
"aa_length": 376,
"cds_start": 917,
"cds_end": null,
"cds_length": 1131,
"cdna_start": 985,
"cdna_end": null,
"cdna_length": 2608,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000955247.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.758G>A",
"hgvs_p": "p.Arg253His",
"transcript": "NM_001199671.2",
"protein_id": "NP_001186600.1",
"transcript_support_level": null,
"aa_start": 253,
"aa_end": null,
"aa_length": 323,
"cds_start": 758,
"cds_end": null,
"cds_length": 972,
"cdna_start": 1634,
"cdna_end": null,
"cdna_length": 6081,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001199671.2"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.758G>A",
"hgvs_p": "p.Arg253His",
"transcript": "NM_001199672.2",
"protein_id": "NP_001186601.1",
"transcript_support_level": null,
"aa_start": 253,
"aa_end": null,
"aa_length": 323,
"cds_start": 758,
"cds_end": null,
"cds_length": 972,
"cdna_start": 1634,
"cdna_end": null,
"cdna_length": 6081,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001199672.2"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "NM_001130674.3",
"protein_id": "NP_001124146.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 819,
"cdna_end": null,
"cdna_length": 5266,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130674.3"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860033.1",
"protein_id": "ENSP00000530092.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1850,
"cdna_end": null,
"cdna_length": 4371,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860033.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860034.1",
"protein_id": "ENSP00000530093.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1511,
"cdna_end": null,
"cdna_length": 3149,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860034.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860035.1",
"protein_id": "ENSP00000530094.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1470,
"cdna_end": null,
"cdna_length": 3108,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860035.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860038.1",
"protein_id": "ENSP00000530097.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 847,
"cdna_end": null,
"cdna_length": 2023,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860038.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860039.1",
"protein_id": "ENSP00000530098.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1856,
"cdna_end": null,
"cdna_length": 2500,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860039.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860040.1",
"protein_id": "ENSP00000530099.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1292,
"cdna_end": null,
"cdna_length": 1861,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860040.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000860041.1",
"protein_id": "ENSP00000530100.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1255,
"cdna_end": null,
"cdna_length": 1824,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000860041.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000918180.1",
"protein_id": "ENSP00000588239.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
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"cdna_start": 1673,
"cdna_end": null,
"cdna_length": 4194,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000918180.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000918181.1",
"protein_id": "ENSP00000588240.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
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"cds_length": 948,
"cdna_start": 1670,
"cdna_end": null,
"cdna_length": 4192,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000918181.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000918182.1",
"protein_id": "ENSP00000588241.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
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"cdna_start": 1228,
"cdna_end": null,
"cdna_length": 3749,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000918182.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000918183.1",
"protein_id": "ENSP00000588242.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 873,
"cdna_end": null,
"cdna_length": 3394,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000918183.1"
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CALU",
"gene_hgnc_id": 1458,
"hgvs_c": "c.734G>A",
"hgvs_p": "p.Arg245His",
"transcript": "ENST00000918184.1",
"protein_id": "ENSP00000588243.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 315,
"cds_start": 734,
"cds_end": null,
"cds_length": 948,
"cdna_start": 1210,
"cdna_end": null,
"cdna_length": 3731,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000918184.1"
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{
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],
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"biotype": "pseudogene",
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],
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"gnomad_exomes_homalt": 0,
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"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.12220653891563416,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.088,
"revel_prediction": "Benign",
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"bayesdelnoaf_score": -0.44,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.084,
"phylop100way_prediction": "Benign",
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"spliceai_max_prediction": "Benign",
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"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -2,
"acmg_classification": "Likely_benign",
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"acmg_by_gene": [
{
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"pathogenic_score": 0,
"criteria": [
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],
"verdict": "Likely_benign",
"transcript": "NM_001199671.2",
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"effects": [
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],
"inheritance_mode": "AR",
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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
}