Variant #0000880231 (NC_000009.11:g.154718G>A, NM_018491.3:c.653C>T (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.154718G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000027
Frequency 2/7308
Freq. EA 1/4594
Freq. AA 1/2714
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 2020-08-29 15:29:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CBWD1 NM_018491.3 ?/? c.653C>T r.(?) p.(Thr218Met)