Variant #0001964701 (NC_000023.10:g.48547416G>A, NM_000377.2:c.1299G>A (WAS))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.48547416G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WAS_000051
Frequency 1/10010
Freq. EA 1/6394
Freq. AA 0/3616
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 09:42:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WAS NM_000377.2 ?/? c.1299G>A r.(=) p.(=)