Variant #0000880237 (NC_000009.11:g.156523A>G, NM_018491.3:c.533T>C (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.156523A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000014
Frequency 5/11532
Freq. EA 0/7576
Freq. AA 5/3956
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 01:28:31 +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.533T>C r.(?) p.(Leu178Ser)