Variant #0000880218 (NC_000009.11:g.121526C>T, NM_018491.3:c.1129G>A (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.121526C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000006
Frequency 1/13002
Freq. EA 1/8596
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 16:29:58 +02:00 (CEST)
Date last edited 2020-08-30 05:33:47 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CBWD1 NM_018491.3 ?/? c.1129G>A r.(?) p.(Val377Met)