Variant #0000082524 (NC_000017.10:g.7591722G>C, NM_001143992.1:c.-159G>C (WRAP53))

Chromosome 17
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7591722G>C
DNA change (hg38) g.7688404G>C
Published as promoter -244G>C
ISCN -
DB-ID WRAP53_000005
Variant remarks -
Reference PubMed: Zhong 2011, Journal: Zhong 2011
ClinVar ID -
dbSNP ID rs17883670
Origin Germline
Segregation -
Frequency 1/16 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-10-27 09:52:58 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WRAP53 NM_001143992.1 -/. _1 c.-159G>C r.(=) p.(=)


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