Variant #0001110444 (NC_000011.9:g.65481166T>C, NC_000011.9(NM_006388.3):c.516+28T>C (KAT5))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.65481166T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KAT5_000044
Frequency 11241/12996
Freq. EA 7860/8594
Freq. AA 3381/4402
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 23:18:54 +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.516+28T>C r.(=) p.(=)