Variant #0000880236 (NC_000009.11:g.154795T>C, NM_018491.3:c.576A>G (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.154795T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000012
Frequency 5486/7182
Freq. EA 3426/4530
Freq. AA 2060/2652
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 01:31:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CBWD1 NM_018491.3 ?/? c.576A>G r.(=) p.(=)