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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: X-71537955-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=71537955&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 71537955,
"ref": "A",
"alt": "C",
"effect": "synonymous_variant",
"transcript": "NM_181672.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "NM_181672.3",
"protein_id": "NP_858058.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1046,
"cds_start": 345,
"cds_end": null,
"cds_length": 3141,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000373719.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_181672.3"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000373719.8",
"protein_id": "ENSP00000362824.3",
"transcript_support_level": 1,
"aa_start": 115,
"aa_end": null,
"aa_length": 1046,
"cds_start": 345,
"cds_end": null,
"cds_length": 3141,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_181672.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000373719.8"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000373701.7",
"protein_id": "ENSP00000362805.3",
"transcript_support_level": 1,
"aa_start": 105,
"aa_end": null,
"aa_length": 1036,
"cds_start": 315,
"cds_end": null,
"cds_length": 3111,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000373701.7"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000925317.1",
"protein_id": "ENSP00000595376.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1044,
"cds_start": 345,
"cds_end": null,
"cds_length": 3135,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925317.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000899817.1",
"protein_id": "ENSP00000569876.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 1040,
"cds_start": 315,
"cds_end": null,
"cds_length": 3123,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899817.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "NM_181673.3",
"protein_id": "NP_858059.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 1036,
"cds_start": 315,
"cds_end": null,
"cds_length": 3111,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_181673.3"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899821.1",
"protein_id": "ENSP00000569880.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1036,
"cds_start": 345,
"cds_end": null,
"cds_length": 3111,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899821.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899818.1",
"protein_id": "ENSP00000569877.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1024,
"cds_start": 345,
"cds_end": null,
"cds_length": 3075,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899818.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000699749.1",
"protein_id": "ENSP00000514559.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1023,
"cds_start": 345,
"cds_end": null,
"cds_length": 3072,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699749.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000925316.1",
"protein_id": "ENSP00000595375.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1016,
"cds_start": 345,
"cds_end": null,
"cds_length": 3051,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925316.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000699782.1",
"protein_id": "ENSP00000514588.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 1013,
"cds_start": 315,
"cds_end": null,
"cds_length": 3042,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699782.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899819.1",
"protein_id": "ENSP00000569878.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1007,
"cds_start": 345,
"cds_end": null,
"cds_length": 3024,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899819.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899814.1",
"protein_id": "ENSP00000569873.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 1004,
"cds_start": 345,
"cds_end": null,
"cds_length": 3015,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899814.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000699784.1",
"protein_id": "ENSP00000514590.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 997,
"cds_start": 315,
"cds_end": null,
"cds_length": 2994,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699784.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000699783.1",
"protein_id": "ENSP00000514589.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 994,
"cds_start": 315,
"cds_end": null,
"cds_length": 2985,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699783.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899815.1",
"protein_id": "ENSP00000569874.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 984,
"cds_start": 345,
"cds_end": null,
"cds_length": 2955,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899815.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000925318.1",
"protein_id": "ENSP00000595377.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 981,
"cds_start": 345,
"cds_end": null,
"cds_length": 2946,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925318.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000899816.1",
"protein_id": "ENSP00000569875.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 974,
"cds_start": 315,
"cds_end": null,
"cds_length": 2925,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899816.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala",
"transcript": "ENST00000899820.1",
"protein_id": "ENSP00000569879.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 954,
"cds_start": 345,
"cds_end": null,
"cds_length": 2865,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899820.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.315A>C",
"hgvs_p": "p.Ala105Ala",
"transcript": "ENST00000899812.1",
"protein_id": "ENSP00000569871.1",
"transcript_support_level": null,
"aa_start": 105,
"aa_end": null,
"aa_length": 944,
"cds_start": 315,
"cds_end": null,
"cds_length": 2835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000899812.1"
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "c.294A>C",
"hgvs_p": "p.Ala98Ala",
"transcript": "ENST00000444774.3",
"protein_id": "ENSP00000399729.1",
"transcript_support_level": 4,
"aa_start": 98,
"aa_end": null,
"aa_length": 155,
"cds_start": 294,
"cds_end": null,
"cds_length": 469,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000444774.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "OGT",
"gene_hgnc_id": 8127,
"hgvs_c": "n.224A>C",
"hgvs_p": null,
"transcript": "ENST00000455587.3",
"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": "ENST00000455587.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
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"gene_symbol": "OGT",
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"feature": "ENST00000488174.5"
},
{
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"protein_coding": false,
"strand": true,
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"biotype": "pseudogene",
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},
{
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"protein_coding": false,
"strand": true,
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],
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"exon_count": 22,
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"gene_symbol": "OGT",
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"hgvs_c": "n.315A>C",
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"transcript": "ENST00000699750.1",
"protein_id": "ENSP00000514560.1",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000699750.1"
},
{
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"protein_coding": false,
"strand": true,
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"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
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"exon_count": 20,
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"gene_symbol": "OGT",
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"transcript": "ENST00000699779.1",
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"feature": "ENST00000699779.1"
},
{
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"non_coding_transcript_exon_variant"
],
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"gene_symbol": "OGT",
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{
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],
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"gene_symbol": "OGT",
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"transcript": "ENST00000699781.1",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000699781.1"
},
{
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"non_coding_transcript_exon_variant"
],
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"gene_symbol": "OGT",
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"hgvs_c": "n.345A>C",
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"transcript": "ENST00000699785.1",
"protein_id": "ENSP00000514591.1",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000699785.1"
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],
"gene_symbol": "OGT",
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"dbsnp": null,
"frequency_reference_population": 9.105851e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 9.10585e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.04899999871850014,
"computational_prediction_selected": "Benign",
"computational_source_selected": "REVEL",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.049,
"revel_prediction": "Benign",
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.65,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.364,
"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": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate,BP7",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 5,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate",
"BP6_Moderate",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "NM_181672.3",
"gene_symbol": "OGT",
"hgnc_id": 8127,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "c.345A>C",
"hgvs_p": "p.Ala115Ala"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}