Variant #0001110459 (NC_000011.9:g.65482032C>A, NM_006388.3:c.658C>A (KAT5))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.65482032C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KAT5_000061
Frequency 2/12996
Freq. EA 0/8594
Freq. AA 2/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 23:18:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KAT5 NM_006388.3 ?/? c.658C>A r.(=) p.(=)