Variant #0000880216 (NC_000009.11:g.121483_121485del, NM_018491.3:c.1170_1172del (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.121483_121485del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000004
Frequency 115/12518
Freq. EA 74/8254
Freq. AA 41/4264
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 01:29:31 +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.1170_1172del r.(?) p.(Glu390del)