Variant #0001900123 (NC_000022.10:g.17072145C>T, NM_014406.4:c.1296G>A (CCT8L2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.17072145C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCT8L2_000019
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 2014-05-11 02:26:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CCT8L2 NM_014406.4 ?/? c.1296G>A r.(=) p.(=)