Variant #0000880226 (NC_000009.11:g.146089A>T, NC_000009.11(NM_018491.3):c.764+13T>A (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.146089A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000018
Frequency 7/5782
Freq. EA 7/3986
Freq. AA 0/1796
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 15:22:58 +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.764+13T>A r.(=) p.(=)