Variant #0001110469 (NC_000011.9:g.65482283C>G, NC_000011.9(NM_006388.3):c.841-9C>G (KAT5))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.65482283C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KAT5_000071
Frequency 1/12996
Freq. EA 0/8594
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 23:18:58 +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.841-9C>G r.(=) p.(=)