Variant #0000830835 (NC_000008.10:g.30942755T>C, NM_000553.4:c.1424T>C (WRN))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.30942755T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WRN_000092
Frequency 1/12984
Freq. EA 0/8582
Freq. AA 1/4402
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:29 +02:00 (CEST)
Date last edited 2019-10-11 17:57:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WRN NM_000553.4 ?/? c.1424T>C r.(?) p.(Met475Thr)