Variant #0001964707 (NC_000023.10:g.48547839C>T, NC_000023.10(NM_000377.2):c.1453+16C>T (WAS))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.48547839C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WAS_000057
Frequency 19/10556
Freq. EA 16/6724
Freq. AA 3/3832
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 16:50:35 +02:00 (CEST)
Date last edited 2013-05-06 09:42:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WAS NM_000377.2 ?/? c.1453+16C>T r.(=) p.(=)