Variant #0001900105 (NC_000022.10:g.17071756T>C, NM_014406.4:c.*11A>G (CCT8L2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.17071756T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCT8L2_000001
Frequency 8/13006
Freq. EA 0/8600
Freq. AA 8/4406
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 16:50:05 +02:00 (CEST)
Date last edited 2014-05-15 20:40:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CCT8L2 NM_014406.4 ?/? c.*11A>G r.(=) p.(=)