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 International |
Created by |
Johan den Dunnen |
Date created |
2015-10-27 09:52:58 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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